{"title":"BIPHEP","description":null,"products":[{"product_id":"q8896-3656","title":"Solvias (S)-MeO-BIPHEP Ligand Kit","description":"\u003cstyle\u003e\n  \/* isQuote *\/\n  div.swatch.clearfix {\n    display:  unset ;\n  }\n\n  \/* Hide sku *\/\n  .product-sku, \n  #leadtimetext {\n    display: none !important;\n  }\n\n  \/* Square brackets *\/\n  span.l_bracket:before {\n    content: \"[\";\n  }\n  span.r_bracket:after {\n    content: \"]\";\n  }\n\n  \/* Hazard Symbols *\/\n  .ghs-symbols-row {\n    display: flex;\n    flex-wrap: wrap;\n    gap: 10px;\n  }\n\n  .hazard-symbol-container {\n    width: 50px;\n  }\n\n  .hazard-symbol {\n    object-fit: contain;\n    aspect-ratio: 1 \/ 1;\n    width: 100%;\n  }\n\n  \/* Section *\/\n  .section-header {\n    font-size: 2rem;\n    font-weight: bold;\n    color: #239ab7;\n    background-color: #f2f2f2;\n    padding: 10px;\n    border-radius: 4px;\n  }\n\n  .section-row {\n    display: grid;\n    grid-template-columns: repeat(8, 1fr);\n    padding: 6px 10px;\n    border-bottom: 1px solid #e0e0e0;\n  }\n\n  .section-content {\n    padding-bottom: 6px;\n  }\n\n  .section-content .section-row:last-child {\n    border-bottom: none;\n  }\n\n  .section-row .row-key {\n    grid-column: 1 \/ 3;\n    font-weight: bold;\n    align-self: center;\n  }\n\n  .section-row .row-value {\n    grid-column: 3 \/ 9;\n  }\n\n  .section-row ul li {\n    line-height: 2rem !important;\n    font-size: 1.3rem;\n  }\n\n  .html-area {\n    padding: 10px;\n    width: 100%;\n    overflow-x: auto;\n  }\n\n  .html-area {\n    padding: 10px;\n  }\n\n  .html-area p {\n    margin: 0 !important;\n  }\n\n  .hazard-grid {\n    display: grid;\n    grid-template-columns: repeat(6, 1fr);\n    gap: 0 10px;\n    font-size: 1.3rem;\n  }\n\n  .reference-item {\n    padding: 10px 10px;\n    border-bottom: 1px solid #e0e0e0;\n  }\n\n  .section-content .reference-item:last-child {\n    border-bottom: none;\n  }\n\n  .reference-item h3 {\n    font-size: 1.5rem !important;\n  }\n\n  .reference-item .publication-item {\n    font-size: 1.3rem !important;\n    line-height: 1.5rem !important;\n  }\n\n  \/* SDS Search *\/\n  .section-row .coa-search-container {\n    display: flex;\n    align-items: center;\n    margin-top: 6px;\n  }\n\n  .section-row .coa-search-container input {\n    border: 1px solid #e0e0e0;\n    height: 2.5rem;\n    border-top-left-radius: 0.5rem !important;\n    border-bottom-left-radius: 0.5rem !important;\n    padding: 3px 5px;\n  }\n\n  .section-row .coa-search-container button {\n    height: 2.5rem;\n    line-height: 2.5rem;\n    border-radius: 0 0.5rem 0.5rem 0;\n  }\n\n  .section-row .coa-search-container button .coa-search-button-content {\n    display: flex;\n    align-items: center;\n    justify-content: center;\n    gap: 3px;\n  }\n\n  .section-row .coa-search-container button .coa-search-button-content .search-spin {\n    display: none;\n    width: 2rem;\n  }\n\n  .section-row .coa-search-container .coa-not-found {\n    display: none;\n    margin: 0 0 0 2rem;\n    color: #ad2031;\n    font-size: 1.3rem;\n  }\n\n  \/* Table *\/\n  .html-area table {\n    width: 100%;\n    border-collapse: collapse;\n    margin: 15px 0;\n  }\n\n  .html-area table th,\n  .html-area table td {\n    border: 1px solid #e0e0e0;\n    padding: 5px 8px;\n  }\n\n  @media (max-width: 600px) {\n    .section-row {\n      grid-template-columns: repeat(1, 1fr);\n    }\n\n    .section-row .row-key {\n      grid-column: 1 \/ 2;\n    }\n\n    .section-row .row-value {\n      grid-column: 1 \/ 2;\n    }\n\n    .hazard-grid {\n      grid-template-columns: repeat(2, 1fr);\n      gap: 0 20px;\n    }\n  }\n  \n\u003c\/style\u003e\n\n\u003cdiv class=\"section\"\u003e\n  \n\n    \u003c!-- Order Info --\u003e\n    \u003ch2 class=\"section-header\"\u003eProduct Information\u003c\/h2\u003e\n    \u003cdiv class=\"section-content\"\u003e\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eProduct Name\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003eSolvias (S)-MeO-BIPHEP Ligand Kit\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n        \n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eBrand Name\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003eUS-Strem\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eProduct Number\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e96-3656\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n\n        \n\n        \n\n        \n\n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eCertificate of Analysis (COA)​\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e\n                \u003cdiv class=\"coa-search-container\"\u003e\n                    \u003cinput id=\"coa-link-input\" type=\"text\" placeholder=\"Enter Lot No.\"\u003e\n                    \u003cbutton id=\"coa-search-button\"\u003e\n                        \u003cdiv class=\"coa-search-button-content\"\u003e\n                            \u003csvg class=\"search-spin\" xmlns=\"http:\/\/www.w3.org\/2000\/svg\" viewbox=\"0 0 200 200\"\u003e\u003cradialgradient id=\"a7\" cx=\".66\" fx=\".66\" cy=\".3125\" fy=\".3125\" gradienttransform=\"scale(1.5)\"\u003e\u003cstop offset=\"0\" stop-color=\"#FFFFFF\"\u003e\u003c\/stop\u003e\u003cstop offset=\".3\" stop-color=\"#FFFFFF\" stop-opacity=\".9\"\u003e\u003c\/stop\u003e\u003cstop offset=\".6\" stop-color=\"#FFFFFF\" stop-opacity=\".6\"\u003e\u003c\/stop\u003e\u003cstop offset=\".8\" stop-color=\"#FFFFFF\" stop-opacity=\".3\"\u003e\u003c\/stop\u003e\u003cstop offset=\"1\" stop-color=\"#FFFFFF\" stop-opacity=\"0\"\u003e\u003c\/stop\u003e\u003c\/radialgradient\u003e\u003ccircle transform-origin=\"center\" fill=\"none\" stroke=\"url(#a7)\" stroke-width=\"15\" stroke-linecap=\"round\" stroke-dasharray=\"200 1000\" stroke-dashoffset=\"0\" cx=\"100\" cy=\"100\" r=\"70\"\u003e\u003canimatetransform type=\"rotate\" attributename=\"transform\" calcmode=\"spline\" dur=\"2\" values=\"360;0\" keytimes=\"0;1\" keysplines=\"0 0 1 1\" repeatcount=\"indefinite\"\u003e\u003c\/animatetransform\u003e\u003c\/circle\u003e\u003ccircle transform-origin=\"center\" fill=\"none\" opacity=\".2\" stroke=\"#FFFFFF\" stroke-width=\"15\" stroke-linecap=\"round\" cx=\"100\" cy=\"100\" r=\"70\"\u003e\u003c\/circle\u003e\u003c\/svg\u003e\n                            \u003cspan\u003eSearch\u003c\/span\u003e\n                        \u003c\/div\u003e\n                    \u003c\/button\u003e\n                    \u003cspan class=\"coa-not-found\"\u003eCOA not found\u003c\/span\u003e\n                \u003c\/div\u003e\n            \u003c\/div\u003e\n        \u003c\/div\u003e\n\n    \u003c\/div\u003e\n\n    \u003c!-- General Info --\u003e\n    \n\n    \u003c!-- Properties --\u003e\n    \n\n    \u003c!-- Safety Info --\u003e\n    \n\n    \u003c!-- Description --\u003e\n    \n\n    \u003c!-- Faq --\u003e\n    \n\n    \u003c!-- References --\u003e\n    \n\n\n    \u003cscript\u003e\n        const coaSearchButton = document.getElementById('coa-search-button');\n        coaSearchButton.addEventListener('click', async function() {\n            const coaLinkInput = document.getElementById('coa-link-input');\n            const spinElement = document.querySelector('.search-spin');\n            const notFoundElement = document.querySelector('.coa-not-found');\n\n            const lot = coaLinkInput.value.trim().toUpperCase();\n            if (lot.length \u003e 0) {\n                spinElement.style.display = 'block';\n                notFoundElement.style.display = 'none';\n\n                const url = `https:\/\/web.jkchemical.com\/partial\/coaFileLotNumber\/${lot}`;\n                await fetch(url).then((res) =\u003e {\n                    if (res.status === 200) {\n                        window.open(url, '_blank');\n                    } else {\n                        notFoundElement.style.display = 'block';\n                    }\n                }).finally(() =\u003e {\n                    spinElement.style.display = 'none';\n                });\n            }\n        });\n    \u003c\/script\u003e\n\n\n\u003c\/div\u003e","brand":"US-Strem","offers":[{"title":"1×1kit","offer_id":45726924505278,"sku":"SC96-3656_1_KIT","price":846.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0506\/0005\/0878\/files\/ee332c00a367e9435177636625c7af78_42e226b5-ef12-4a01-930c-bb878aa6d71b.jpg?v=1788898491"},{"product_id":"q8896-3655","title":"Solvias (R)-MeO-BIPHEP Ligand Kit","description":"\u003cstyle\u003e\n  \/* isQuote *\/\n  div.swatch.clearfix {\n    display:  unset ;\n  }\n\n  \/* Hide sku *\/\n  .product-sku, \n  #leadtimetext {\n    display: none !important;\n  }\n\n  \/* Square brackets *\/\n  span.l_bracket:before {\n    content: \"[\";\n  }\n  span.r_bracket:after {\n    content: \"]\";\n  }\n\n  \/* Hazard Symbols *\/\n  .ghs-symbols-row {\n    display: flex;\n    flex-wrap: wrap;\n    gap: 10px;\n  }\n\n  .hazard-symbol-container {\n    width: 50px;\n  }\n\n  .hazard-symbol {\n    object-fit: contain;\n    aspect-ratio: 1 \/ 1;\n    width: 100%;\n  }\n\n  \/* Section *\/\n  .section-header {\n    font-size: 2rem;\n    font-weight: bold;\n    color: #239ab7;\n    background-color: #f2f2f2;\n    padding: 10px;\n    border-radius: 4px;\n  }\n\n  .section-row {\n    display: grid;\n    grid-template-columns: repeat(8, 1fr);\n    padding: 6px 10px;\n    border-bottom: 1px solid #e0e0e0;\n  }\n\n  .section-content {\n    padding-bottom: 6px;\n  }\n\n  .section-content .section-row:last-child {\n    border-bottom: none;\n  }\n\n  .section-row .row-key {\n    grid-column: 1 \/ 3;\n    font-weight: bold;\n    align-self: center;\n  }\n\n  .section-row .row-value {\n    grid-column: 3 \/ 9;\n  }\n\n  .section-row ul li {\n    line-height: 2rem !important;\n    font-size: 1.3rem;\n  }\n\n  .html-area {\n    padding: 10px;\n    width: 100%;\n    overflow-x: auto;\n  }\n\n  .html-area {\n    padding: 10px;\n  }\n\n  .html-area p {\n    margin: 0 !important;\n  }\n\n  .hazard-grid {\n    display: grid;\n    grid-template-columns: repeat(6, 1fr);\n    gap: 0 10px;\n    font-size: 1.3rem;\n  }\n\n  .reference-item {\n    padding: 10px 10px;\n    border-bottom: 1px solid #e0e0e0;\n  }\n\n  .section-content .reference-item:last-child {\n    border-bottom: none;\n  }\n\n  .reference-item h3 {\n    font-size: 1.5rem !important;\n  }\n\n  .reference-item .publication-item {\n    font-size: 1.3rem !important;\n    line-height: 1.5rem !important;\n  }\n\n  \/* SDS Search *\/\n  .section-row .coa-search-container {\n    display: flex;\n    align-items: center;\n    margin-top: 6px;\n  }\n\n  .section-row .coa-search-container input {\n    border: 1px solid #e0e0e0;\n    height: 2.5rem;\n    border-top-left-radius: 0.5rem !important;\n    border-bottom-left-radius: 0.5rem !important;\n    padding: 3px 5px;\n  }\n\n  .section-row .coa-search-container button {\n    height: 2.5rem;\n    line-height: 2.5rem;\n    border-radius: 0 0.5rem 0.5rem 0;\n  }\n\n  .section-row .coa-search-container button .coa-search-button-content {\n    display: flex;\n    align-items: center;\n    justify-content: center;\n    gap: 3px;\n  }\n\n  .section-row .coa-search-container button .coa-search-button-content .search-spin {\n    display: none;\n    width: 2rem;\n  }\n\n  .section-row .coa-search-container .coa-not-found {\n    display: none;\n    margin: 0 0 0 2rem;\n    color: #ad2031;\n    font-size: 1.3rem;\n  }\n\n  \/* Table *\/\n  .html-area table {\n    width: 100%;\n    border-collapse: collapse;\n    margin: 15px 0;\n  }\n\n  .html-area table th,\n  .html-area table td {\n    border: 1px solid #e0e0e0;\n    padding: 5px 8px;\n  }\n\n  @media (max-width: 600px) {\n    .section-row {\n      grid-template-columns: repeat(1, 1fr);\n    }\n\n    .section-row .row-key {\n      grid-column: 1 \/ 2;\n    }\n\n    .section-row .row-value {\n      grid-column: 1 \/ 2;\n    }\n\n    .hazard-grid {\n      grid-template-columns: repeat(2, 1fr);\n      gap: 0 20px;\n    }\n  }\n  \n\u003c\/style\u003e\n\n\u003cdiv class=\"section\"\u003e\n  \n\n    \u003c!-- Order Info --\u003e\n    \u003ch2 class=\"section-header\"\u003eProduct Information\u003c\/h2\u003e\n    \u003cdiv class=\"section-content\"\u003e\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eProduct Name\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003eSolvias (R)-MeO-BIPHEP Ligand Kit\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n        \n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eBrand Name\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003eUS-Strem\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eProduct Number\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e96-3655\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n\n        \n\n        \n\n        \n\n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eCertificate of Analysis (COA)​\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e\n                \u003cdiv class=\"coa-search-container\"\u003e\n                    \u003cinput id=\"coa-link-input\" type=\"text\" placeholder=\"Enter Lot No.\"\u003e\n                    \u003cbutton id=\"coa-search-button\"\u003e\n                        \u003cdiv class=\"coa-search-button-content\"\u003e\n                            \u003csvg class=\"search-spin\" xmlns=\"http:\/\/www.w3.org\/2000\/svg\" viewbox=\"0 0 200 200\"\u003e\u003cradialgradient id=\"a7\" cx=\".66\" fx=\".66\" cy=\".3125\" fy=\".3125\" gradienttransform=\"scale(1.5)\"\u003e\u003cstop offset=\"0\" stop-color=\"#FFFFFF\"\u003e\u003c\/stop\u003e\u003cstop offset=\".3\" stop-color=\"#FFFFFF\" stop-opacity=\".9\"\u003e\u003c\/stop\u003e\u003cstop offset=\".6\" stop-color=\"#FFFFFF\" stop-opacity=\".6\"\u003e\u003c\/stop\u003e\u003cstop offset=\".8\" stop-color=\"#FFFFFF\" stop-opacity=\".3\"\u003e\u003c\/stop\u003e\u003cstop offset=\"1\" stop-color=\"#FFFFFF\" stop-opacity=\"0\"\u003e\u003c\/stop\u003e\u003c\/radialgradient\u003e\u003ccircle transform-origin=\"center\" fill=\"none\" stroke=\"url(#a7)\" stroke-width=\"15\" stroke-linecap=\"round\" stroke-dasharray=\"200 1000\" stroke-dashoffset=\"0\" cx=\"100\" cy=\"100\" r=\"70\"\u003e\u003canimatetransform type=\"rotate\" attributename=\"transform\" calcmode=\"spline\" dur=\"2\" values=\"360;0\" keytimes=\"0;1\" keysplines=\"0 0 1 1\" repeatcount=\"indefinite\"\u003e\u003c\/animatetransform\u003e\u003c\/circle\u003e\u003ccircle transform-origin=\"center\" fill=\"none\" opacity=\".2\" stroke=\"#FFFFFF\" stroke-width=\"15\" stroke-linecap=\"round\" cx=\"100\" cy=\"100\" r=\"70\"\u003e\u003c\/circle\u003e\u003c\/svg\u003e\n                            \u003cspan\u003eSearch\u003c\/span\u003e\n                        \u003c\/div\u003e\n                    \u003c\/button\u003e\n                    \u003cspan class=\"coa-not-found\"\u003eCOA not found\u003c\/span\u003e\n                \u003c\/div\u003e\n            \u003c\/div\u003e\n        \u003c\/div\u003e\n\n    \u003c\/div\u003e\n\n    \u003c!-- General Info --\u003e\n    \n\n    \u003c!-- Properties --\u003e\n    \n\n    \u003c!-- Safety Info --\u003e\n    \n\n    \u003c!-- Description --\u003e\n    \n\n    \u003c!-- Faq --\u003e\n    \n\n    \u003c!-- References --\u003e\n    \n\n\n    \u003cscript\u003e\n        const coaSearchButton = document.getElementById('coa-search-button');\n        coaSearchButton.addEventListener('click', async function() {\n            const coaLinkInput = document.getElementById('coa-link-input');\n            const spinElement = document.querySelector('.search-spin');\n            const notFoundElement = document.querySelector('.coa-not-found');\n\n            const lot = coaLinkInput.value.trim().toUpperCase();\n            if (lot.length \u003e 0) {\n                spinElement.style.display = 'block';\n                notFoundElement.style.display = 'none';\n\n                const url = `https:\/\/web.jkchemical.com\/partial\/coaFileLotNumber\/${lot}`;\n                await fetch(url).then((res) =\u003e {\n                    if (res.status === 200) {\n                        window.open(url, '_blank');\n                    } else {\n                        notFoundElement.style.display = 'block';\n                    }\n                }).finally(() =\u003e {\n                    spinElement.style.display = 'none';\n                });\n            }\n        });\n    \u003c\/script\u003e\n\n\n\u003c\/div\u003e","brand":"US-Strem","offers":[{"title":"1×1kit","offer_id":45727193923774,"sku":"SC96-3655_1_KIT","price":658.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0506\/0005\/0878\/files\/ee332c00a367e9435177636625c7af78_d91a0542-b870-4233-9ee5-8702cd946762.jpg?v=1788898494"},{"product_id":"q8815-0652","title":"(R)-(-)-2,2'-Bis[di(3,5-di-i-propyl-4-dimethylaminophenyl)phosphino]-6,6'-dimethoxy-1,1'-biphenyl, min. 97% | 352655-40-4","description":"\u003cstyle\u003e\n  \/* isQuote *\/\n  div.swatch.clearfix {\n    display:  unset ;\n  }\n\n  \/* Hide sku *\/\n  .product-sku, \n  #leadtimetext {\n    display: none !important;\n  }\n\n  \/* Square brackets *\/\n  span.l_bracket:before {\n    content: \"[\";\n  }\n  span.r_bracket:after {\n    content: \"]\";\n  }\n\n  \/* Hazard Symbols *\/\n  .ghs-symbols-row {\n    display: flex;\n    flex-wrap: wrap;\n    gap: 10px;\n  }\n\n  .hazard-symbol-container {\n    width: 50px;\n  }\n\n  .hazard-symbol {\n    object-fit: contain;\n    aspect-ratio: 1 \/ 1;\n    width: 100%;\n  }\n\n  \/* Section *\/\n  .section-header {\n    font-size: 2rem;\n    font-weight: bold;\n    color: #239ab7;\n    background-color: #f2f2f2;\n    padding: 10px;\n    border-radius: 4px;\n  }\n\n  .section-row {\n    display: grid;\n    grid-template-columns: repeat(8, 1fr);\n    padding: 6px 10px;\n    border-bottom: 1px solid #e0e0e0;\n  }\n\n  .section-content {\n    padding-bottom: 6px;\n  }\n\n  .section-content .section-row:last-child {\n    border-bottom: none;\n  }\n\n  .section-row .row-key {\n    grid-column: 1 \/ 3;\n    font-weight: bold;\n    align-self: center;\n  }\n\n  .section-row .row-value {\n    grid-column: 3 \/ 9;\n  }\n\n  .section-row ul li {\n    line-height: 2rem !important;\n    font-size: 1.3rem;\n  }\n\n  .html-area {\n    padding: 10px;\n    width: 100%;\n    overflow-x: auto;\n  }\n\n  .html-area {\n    padding: 10px;\n  }\n\n  .html-area p {\n    margin: 0 !important;\n  }\n\n  .hazard-grid {\n    display: grid;\n    grid-template-columns: repeat(6, 1fr);\n    gap: 0 10px;\n    font-size: 1.3rem;\n  }\n\n  .reference-item {\n    padding: 10px 10px;\n    border-bottom: 1px solid #e0e0e0;\n  }\n\n  .section-content .reference-item:last-child {\n    border-bottom: none;\n  }\n\n  .reference-item h3 {\n    font-size: 1.5rem !important;\n  }\n\n  .reference-item .publication-item {\n    font-size: 1.3rem !important;\n    line-height: 1.5rem !important;\n  }\n\n  \/* SDS Search *\/\n  .section-row .coa-search-container {\n    display: flex;\n    align-items: center;\n    margin-top: 6px;\n  }\n\n  .section-row .coa-search-container input {\n    border: 1px solid #e0e0e0;\n    height: 2.5rem;\n    border-top-left-radius: 0.5rem !important;\n    border-bottom-left-radius: 0.5rem !important;\n    padding: 3px 5px;\n  }\n\n  .section-row .coa-search-container button {\n    height: 2.5rem;\n    line-height: 2.5rem;\n    border-radius: 0 0.5rem 0.5rem 0;\n  }\n\n  .section-row .coa-search-container button .coa-search-button-content {\n    display: flex;\n    align-items: center;\n    justify-content: center;\n    gap: 3px;\n  }\n\n  .section-row .coa-search-container button .coa-search-button-content .search-spin {\n    display: none;\n    width: 2rem;\n  }\n\n  .section-row .coa-search-container .coa-not-found {\n    display: none;\n    margin: 0 0 0 2rem;\n    color: #ad2031;\n    font-size: 1.3rem;\n  }\n\n  \/* Table *\/\n  .html-area table {\n    width: 100%;\n    border-collapse: collapse;\n    margin: 15px 0;\n  }\n\n  .html-area table th,\n  .html-area table td {\n    border: 1px solid #e0e0e0;\n    padding: 5px 8px;\n  }\n\n  @media (max-width: 600px) {\n    .section-row {\n      grid-template-columns: repeat(1, 1fr);\n    }\n\n    .section-row .row-key {\n      grid-column: 1 \/ 2;\n    }\n\n    .section-row .row-value {\n      grid-column: 1 \/ 2;\n    }\n\n    .hazard-grid {\n      grid-template-columns: repeat(2, 1fr);\n      gap: 0 20px;\n    }\n  }\n  \n\u003c\/style\u003e\n\n\u003cdiv class=\"section\"\u003e\n  \n\n    \u003c!-- Order Info --\u003e\n    \u003ch2 class=\"section-header\"\u003eProduct Information\u003c\/h2\u003e\n    \u003cdiv class=\"section-content\"\u003e\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eProduct Name\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e(R)-(-)-2,2'-Bis\u003cspan class=\"l_bracket\"\u003e\u003c\/span\u003edi(3,5-di-i-propyl-4-dimethylaminophenyl)phosphino\u003cspan class=\"r_bracket\"\u003e\u003c\/span\u003e-6,6'-dimethoxy-1,1'-biphenyl, min. 97%\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n        \n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eBrand Name\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003eUS-Strem\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eProduct Number\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e15-0652\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eCAS\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e352655-40-4\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n\n        \n\n        \n\n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eCertificate of Analysis (COA)​\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e\n                \u003cdiv class=\"coa-search-container\"\u003e\n                    \u003cinput id=\"coa-link-input\" type=\"text\" placeholder=\"Enter Lot No.\"\u003e\n                    \u003cbutton id=\"coa-search-button\"\u003e\n                        \u003cdiv class=\"coa-search-button-content\"\u003e\n                            \u003csvg class=\"search-spin\" xmlns=\"http:\/\/www.w3.org\/2000\/svg\" viewbox=\"0 0 200 200\"\u003e\u003cradialgradient id=\"a7\" cx=\".66\" fx=\".66\" cy=\".3125\" fy=\".3125\" gradienttransform=\"scale(1.5)\"\u003e\u003cstop offset=\"0\" stop-color=\"#FFFFFF\"\u003e\u003c\/stop\u003e\u003cstop offset=\".3\" stop-color=\"#FFFFFF\" stop-opacity=\".9\"\u003e\u003c\/stop\u003e\u003cstop offset=\".6\" stop-color=\"#FFFFFF\" stop-opacity=\".6\"\u003e\u003c\/stop\u003e\u003cstop offset=\".8\" stop-color=\"#FFFFFF\" stop-opacity=\".3\"\u003e\u003c\/stop\u003e\u003cstop offset=\"1\" stop-color=\"#FFFFFF\" stop-opacity=\"0\"\u003e\u003c\/stop\u003e\u003c\/radialgradient\u003e\u003ccircle transform-origin=\"center\" fill=\"none\" stroke=\"url(#a7)\" stroke-width=\"15\" stroke-linecap=\"round\" stroke-dasharray=\"200 1000\" stroke-dashoffset=\"0\" cx=\"100\" cy=\"100\" r=\"70\"\u003e\u003canimatetransform type=\"rotate\" attributename=\"transform\" calcmode=\"spline\" dur=\"2\" values=\"360;0\" keytimes=\"0;1\" keysplines=\"0 0 1 1\" repeatcount=\"indefinite\"\u003e\u003c\/animatetransform\u003e\u003c\/circle\u003e\u003ccircle transform-origin=\"center\" fill=\"none\" opacity=\".2\" stroke=\"#FFFFFF\" stroke-width=\"15\" stroke-linecap=\"round\" cx=\"100\" cy=\"100\" r=\"70\"\u003e\u003c\/circle\u003e\u003c\/svg\u003e\n                            \u003cspan\u003eSearch\u003c\/span\u003e\n                        \u003c\/div\u003e\n                    \u003c\/button\u003e\n                    \u003cspan class=\"coa-not-found\"\u003eCOA not found\u003c\/span\u003e\n                \u003c\/div\u003e\n            \u003c\/div\u003e\n        \u003c\/div\u003e\n\n    \u003c\/div\u003e\n\n    \u003c!-- General Info --\u003e\n    \n        \u003ch2 class=\"section-header\"\u003eGeneral Information\u003c\/h2\u003e\n        \u003cdiv class=\"section-content\"\u003e\n            \n\n            \n            \u003cdiv class=\"section-row\"\u003e\n                \u003cdiv class=\"row-key\"\u003ePubChem CID\u003c\/div\u003e\n                \u003cdiv class=\"row-value\"\u003e46910330\u003c\/div\u003e\n            \u003c\/div\u003e\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eIUPAC Name\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003e4-\u003cspan class=\"l_bracket\"\u003e\u003c\/span\u003e\u003cspan class=\"l_bracket\"\u003e\u003c\/span\u003e2-\u003cspan class=\"l_bracket\"\u003e\u003c\/span\u003e2-bis\u003cspan class=\"l_bracket\"\u003e\u003c\/span\u003e4-(dimethylamino)-3,5-di(propan-2-yl)phenyl\u003cspan class=\"r_bracket\"\u003e\u003c\/span\u003ephosphanyl-6-methoxyphenyl\u003cspan class=\"r_bracket\"\u003e\u003c\/span\u003e-3-methoxyphenyl\u003cspan class=\"r_bracket\"\u003e\u003c\/span\u003e-\u003cspan class=\"l_bracket\"\u003e\u003c\/span\u003e4-(dimethylamino)-3,5-di(propan-2-yl)phenyl\u003cspan class=\"r_bracket\"\u003e\u003c\/span\u003ephosphanyl\u003cspan class=\"r_bracket\"\u003e\u003c\/span\u003e-N,N-dimethyl-2,6-di(propan-2-yl)aniline\u003c\/div\u003e\n                \u003c\/div\u003e\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eInChI Key\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003eSBQGDYGNDIQAIT-UHFFFAOYSA-N\u003c\/div\u003e\n                \u003c\/div\u003e\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eSMILES\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003eCC(C)C1=CC(=CC(=C1N(C)C)C(C)C)P(C2=CC=CC(=C2C3=C(C=CC=C3P(C4=CC(=C(C(=C4)C(C)C)N(C)C)C(C)C)C5=CC(=C(C(=C5)C(C)C)N(C)C)C(C)C)OC)OC)C6=CC(=C(C(=C6)C(C)C)N(C)C)C(C)C\u003c\/div\u003e\n                \u003c\/div\u003e\n            \n        \u003c\/div\u003e\n    \n\n    \u003c!-- Properties --\u003e\n    \n\n    \u003c!-- Safety Info --\u003e\n    \n        \u003ch2 class=\"section-header\"\u003eSafety Information\u003c\/h2\u003e\n        \u003cdiv class=\"section-content\"\u003e\n            \n\n            \n\n            \n\n            \n\n            \n\n            \n\n            \n\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eStorage Condition\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003e\n                        Store at 2-8℃\n                    \u003c\/div\u003e\n                \u003c\/div\u003e\n            \n        \u003c\/div\u003e\n    \n\n    \u003c!-- Description --\u003e\n    \n\n    \u003c!-- Faq --\u003e\n    \n\n    \u003c!-- References --\u003e\n    \n    \u003ch2 class=\"section-header\"\u003e\n        \u003cspan style=\"display: block;\"\u003eReferences\u003c\/span\u003e\n        \u003cspan style=\"display: block; font-size: 1.2rem; color: #777; font-weight: lighter;\"\u003eData Source From Pubchem\u003c\/span\u003e\n    \u003c\/h2\u003e\n    \u003cdiv class=\"section-content\"\u003e\n        \n            \u003cdiv class=\"reference-item\"\u003e\n                \n                    \n                    \u003ca href=\"https:\/\/science-of-synthesis.thieme.com\/app\/text\/?id=SD-147-00239\" target=\"_blank\" rel=\"noopener noreferrer\"\u003e\n                        \u003ch3\u003eEnantioselective N2-Allylation of Pyridazin-3(2H)-ones with Terminal Allenes\u003c\/h3\u003e\n                    \u003c\/a\u003e\n                    \n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Name: Science of Synthesis\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Date: 2023\u003c\/div\u003e\n                \n\n                \n            \u003c\/div\u003e\n        \n    \u003c\/div\u003e\n    \n\n\n    \u003cscript\u003e\n        const coaSearchButton = document.getElementById('coa-search-button');\n        coaSearchButton.addEventListener('click', async function() {\n            const coaLinkInput = document.getElementById('coa-link-input');\n            const spinElement = document.querySelector('.search-spin');\n            const notFoundElement = document.querySelector('.coa-not-found');\n\n            const lot = coaLinkInput.value.trim().toUpperCase();\n            if (lot.length \u003e 0) {\n                spinElement.style.display = 'block';\n                notFoundElement.style.display = 'none';\n\n                const url = `https:\/\/web.jkchemical.com\/partial\/coaFileLotNumber\/${lot}`;\n                await fetch(url).then((res) =\u003e {\n                    if (res.status === 200) {\n                        window.open(url, '_blank');\n                    } else {\n                        notFoundElement.style.display = 'block';\n                    }\n                }).finally(() =\u003e {\n                    spinElement.style.display = 'none';\n                });\n            }\n        });\n    \u003c\/script\u003e\n\n\n\u003c\/div\u003e","brand":"US-Strem","offers":[{"title":"1×500mg","offer_id":45724372435134,"sku":"SC15-0652_500_MG","price":366.0,"currency_code":"USD","in_stock":true},{"title":"1×2g","offer_id":45724372467902,"sku":"SC15-0652_2_G","price":1244.0,"currency_code":"USD","in_stock":true},{"title":"1×10g","offer_id":45724372500670,"sku":"SC15-0652_10_G","price":4969.0,"currency_code":"USD","in_stock":true},{"title":"1×100mg","offer_id":45724372533438,"sku":"SC15-0652_100_MG","price":99.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0506\/0005\/0878\/files\/e4759953edb0117721ca7f29aeed90a6.jpg?v=1788907816"},{"product_id":"q8815-0653","title":"(S)-(+)-2,2'-Bis[di(3,5-di-i-propyl-4-dimethylaminophenyl)phosphino]-6,6'-dimethoxy-1,1'-biphenyl, min. 97% | 919338-66-2","description":"\u003cstyle\u003e\n  \/* isQuote *\/\n  div.swatch.clearfix {\n    display:  unset ;\n  }\n\n  \/* Hide sku *\/\n  .product-sku, \n  #leadtimetext {\n    display: none !important;\n  }\n\n  \/* Square brackets *\/\n  span.l_bracket:before {\n    content: \"[\";\n  }\n  span.r_bracket:after {\n    content: \"]\";\n  }\n\n  \/* Hazard Symbols *\/\n  .ghs-symbols-row {\n    display: flex;\n    flex-wrap: wrap;\n    gap: 10px;\n  }\n\n  .hazard-symbol-container {\n    width: 50px;\n  }\n\n  .hazard-symbol {\n    object-fit: contain;\n    aspect-ratio: 1 \/ 1;\n    width: 100%;\n  }\n\n  \/* Section *\/\n  .section-header {\n    font-size: 2rem;\n    font-weight: bold;\n    color: #239ab7;\n    background-color: #f2f2f2;\n    padding: 10px;\n    border-radius: 4px;\n  }\n\n  .section-row {\n    display: grid;\n    grid-template-columns: repeat(8, 1fr);\n    padding: 6px 10px;\n    border-bottom: 1px solid #e0e0e0;\n  }\n\n  .section-content {\n    padding-bottom: 6px;\n  }\n\n  .section-content .section-row:last-child {\n    border-bottom: none;\n  }\n\n  .section-row .row-key {\n    grid-column: 1 \/ 3;\n    font-weight: bold;\n    align-self: center;\n  }\n\n  .section-row .row-value {\n    grid-column: 3 \/ 9;\n  }\n\n  .section-row ul li {\n    line-height: 2rem !important;\n    font-size: 1.3rem;\n  }\n\n  .html-area {\n    padding: 10px;\n    width: 100%;\n    overflow-x: auto;\n  }\n\n  .html-area {\n    padding: 10px;\n  }\n\n  .html-area p {\n    margin: 0 !important;\n  }\n\n  .hazard-grid {\n    display: grid;\n    grid-template-columns: repeat(6, 1fr);\n    gap: 0 10px;\n    font-size: 1.3rem;\n  }\n\n  .reference-item {\n    padding: 10px 10px;\n    border-bottom: 1px solid #e0e0e0;\n  }\n\n  .section-content .reference-item:last-child {\n    border-bottom: none;\n  }\n\n  .reference-item h3 {\n    font-size: 1.5rem !important;\n  }\n\n  .reference-item .publication-item {\n    font-size: 1.3rem !important;\n    line-height: 1.5rem !important;\n  }\n\n  \/* SDS Search *\/\n  .section-row .coa-search-container {\n    display: flex;\n    align-items: center;\n    margin-top: 6px;\n  }\n\n  .section-row .coa-search-container input {\n    border: 1px solid #e0e0e0;\n    height: 2.5rem;\n    border-top-left-radius: 0.5rem !important;\n    border-bottom-left-radius: 0.5rem !important;\n    padding: 3px 5px;\n  }\n\n  .section-row .coa-search-container button {\n    height: 2.5rem;\n    line-height: 2.5rem;\n    border-radius: 0 0.5rem 0.5rem 0;\n  }\n\n  .section-row .coa-search-container button .coa-search-button-content {\n    display: flex;\n    align-items: center;\n    justify-content: center;\n    gap: 3px;\n  }\n\n  .section-row .coa-search-container button .coa-search-button-content .search-spin {\n    display: none;\n    width: 2rem;\n  }\n\n  .section-row .coa-search-container .coa-not-found {\n    display: none;\n    margin: 0 0 0 2rem;\n    color: #ad2031;\n    font-size: 1.3rem;\n  }\n\n  \/* Table *\/\n  .html-area table {\n    width: 100%;\n    border-collapse: collapse;\n    margin: 15px 0;\n  }\n\n  .html-area table th,\n  .html-area table td {\n    border: 1px solid #e0e0e0;\n    padding: 5px 8px;\n  }\n\n  @media (max-width: 600px) {\n    .section-row {\n      grid-template-columns: repeat(1, 1fr);\n    }\n\n    .section-row .row-key {\n      grid-column: 1 \/ 2;\n    }\n\n    .section-row .row-value {\n      grid-column: 1 \/ 2;\n    }\n\n    .hazard-grid {\n      grid-template-columns: repeat(2, 1fr);\n      gap: 0 20px;\n    }\n  }\n  \n\u003c\/style\u003e\n\n\u003cdiv class=\"section\"\u003e\n  \n\n    \u003c!-- Order Info --\u003e\n    \u003ch2 class=\"section-header\"\u003eProduct Information\u003c\/h2\u003e\n    \u003cdiv class=\"section-content\"\u003e\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eProduct Name\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e(S)-(+)-2,2'-Bis\u003cspan class=\"l_bracket\"\u003e\u003c\/span\u003edi(3,5-di-i-propyl-4-dimethylaminophenyl)phosphino\u003cspan class=\"r_bracket\"\u003e\u003c\/span\u003e-6,6'-dimethoxy-1,1'-biphenyl, min. 97%\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n        \n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eBrand Name\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003eUS-Strem\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eProduct Number\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e15-0653\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eCAS\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e919338-66-2\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n\n        \n\n        \n\n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eCertificate of Analysis (COA)​\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e\n                \u003cdiv class=\"coa-search-container\"\u003e\n                    \u003cinput id=\"coa-link-input\" type=\"text\" placeholder=\"Enter Lot No.\"\u003e\n                    \u003cbutton id=\"coa-search-button\"\u003e\n                        \u003cdiv class=\"coa-search-button-content\"\u003e\n                            \u003csvg class=\"search-spin\" xmlns=\"http:\/\/www.w3.org\/2000\/svg\" viewbox=\"0 0 200 200\"\u003e\u003cradialgradient id=\"a7\" cx=\".66\" fx=\".66\" cy=\".3125\" fy=\".3125\" gradienttransform=\"scale(1.5)\"\u003e\u003cstop offset=\"0\" stop-color=\"#FFFFFF\"\u003e\u003c\/stop\u003e\u003cstop offset=\".3\" stop-color=\"#FFFFFF\" stop-opacity=\".9\"\u003e\u003c\/stop\u003e\u003cstop offset=\".6\" stop-color=\"#FFFFFF\" stop-opacity=\".6\"\u003e\u003c\/stop\u003e\u003cstop offset=\".8\" stop-color=\"#FFFFFF\" stop-opacity=\".3\"\u003e\u003c\/stop\u003e\u003cstop offset=\"1\" stop-color=\"#FFFFFF\" stop-opacity=\"0\"\u003e\u003c\/stop\u003e\u003c\/radialgradient\u003e\u003ccircle transform-origin=\"center\" fill=\"none\" stroke=\"url(#a7)\" stroke-width=\"15\" stroke-linecap=\"round\" stroke-dasharray=\"200 1000\" stroke-dashoffset=\"0\" cx=\"100\" cy=\"100\" r=\"70\"\u003e\u003canimatetransform type=\"rotate\" attributename=\"transform\" calcmode=\"spline\" dur=\"2\" values=\"360;0\" keytimes=\"0;1\" keysplines=\"0 0 1 1\" repeatcount=\"indefinite\"\u003e\u003c\/animatetransform\u003e\u003c\/circle\u003e\u003ccircle transform-origin=\"center\" fill=\"none\" opacity=\".2\" stroke=\"#FFFFFF\" stroke-width=\"15\" stroke-linecap=\"round\" cx=\"100\" cy=\"100\" r=\"70\"\u003e\u003c\/circle\u003e\u003c\/svg\u003e\n                            \u003cspan\u003eSearch\u003c\/span\u003e\n                        \u003c\/div\u003e\n                    \u003c\/button\u003e\n                    \u003cspan class=\"coa-not-found\"\u003eCOA not found\u003c\/span\u003e\n                \u003c\/div\u003e\n            \u003c\/div\u003e\n        \u003c\/div\u003e\n\n    \u003c\/div\u003e\n\n    \u003c!-- General Info --\u003e\n    \n        \u003ch2 class=\"section-header\"\u003eGeneral Information\u003c\/h2\u003e\n        \u003cdiv class=\"section-content\"\u003e\n            \n\n            \n            \u003cdiv class=\"section-row\"\u003e\n                \u003cdiv class=\"row-key\"\u003ePubChem CID\u003c\/div\u003e\n                \u003cdiv class=\"row-value\"\u003e46910330\u003c\/div\u003e\n            \u003c\/div\u003e\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eIUPAC Name\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003e4-\u003cspan class=\"l_bracket\"\u003e\u003c\/span\u003e\u003cspan class=\"l_bracket\"\u003e\u003c\/span\u003e2-\u003cspan 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--\u003e\n    \n        \u003ch2 class=\"section-header\"\u003eGeneral Information\u003c\/h2\u003e\n        \u003cdiv class=\"section-content\"\u003e\n            \n\n            \n            \u003cdiv class=\"section-row\"\u003e\n                \u003cdiv class=\"row-key\"\u003ePubChem CID\u003c\/div\u003e\n                \u003cdiv class=\"row-value\"\u003e4246603\u003c\/div\u003e\n            \u003c\/div\u003e\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eIUPAC Name\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003e\n\u003cspan class=\"l_bracket\"\u003e\u003c\/span\u003e2-(2-diphenylphosphanyl-6-methoxyphenyl)-3-methoxyphenyl\u003cspan class=\"r_bracket\"\u003e\u003c\/span\u003e-diphenylphosphane\u003c\/div\u003e\n                \u003c\/div\u003e\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eInChI Key\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003eKRJVQCZJJSUHHO-UHFFFAOYSA-N\u003c\/div\u003e\n                \u003c\/div\u003e\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eSMILES\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003eCOC1=C(C(=CC=C1)P(C2=CC=CC=C2)C3=CC=CC=C3)C4=C(C=CC=C4P(C5=CC=CC=C5)C6=CC=CC=C6)OC\u003c\/div\u003e\n                \u003c\/div\u003e\n            \n        \u003c\/div\u003e\n    \n\n    \u003c!-- Properties --\u003e\n    \n\n    \u003c!-- Safety Info --\u003e\n    \n\n    \u003c!-- Description --\u003e\n    \n\n    \u003c!-- Faq --\u003e\n    \n\n    \u003c!-- References --\u003e\n    \n    \u003ch2 class=\"section-header\"\u003e\n        \u003cspan style=\"display: block;\"\u003eReferences\u003c\/span\u003e\n        \u003cspan style=\"display: block; font-size: 1.2rem; color: #777; font-weight: lighter;\"\u003eData Source From Pubchem\u003c\/span\u003e\n    \u003c\/h2\u003e\n    \u003cdiv class=\"section-content\"\u003e\n        \n            \u003cdiv class=\"reference-item\"\u003e\n                \n                    \n                    \u003ca href=\"https:\/\/doi.org\/10.1038\/s44160-025-00839-y\" target=\"_blank\" rel=\"noopener noreferrer\"\u003e\n                        \u003ch3\u003eStrain-dependent enantioselectivity in mechanochemically coupled catalytic hydrogenation\u003c\/h3\u003e\n                    \u003c\/a\u003e\n                    \n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Name: Nature Synthesis\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Date: 2025-07-17\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003eDOI: 10.1038\/s44160-025-00839-y\u003c\/div\u003e\n                \n            \u003c\/div\u003e\n        \n            \u003cdiv class=\"reference-item\"\u003e\n                \n                    \n                    \u003ca href=\"https:\/\/doi.org\/10.1038\/s44160-024-00604-7\" target=\"_blank\" rel=\"noopener noreferrer\"\u003e\n                        \u003ch3\u003eRh-catalysed enantioselective [2+2+1] cycloaddition reactions using three different 2π-components\u003c\/h3\u003e\n                    \u003c\/a\u003e\n                    \n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Name: Nature Synthesis\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Date: 2024-07-17\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003eDOI: 10.1038\/s44160-024-00604-7\u003c\/div\u003e\n                \n            \u003c\/div\u003e\n        \n            \u003cdiv class=\"reference-item\"\u003e\n                \n                    \n                    \u003ca href=\"https:\/\/doi.org\/10.1038\/s44160-024-00555-z\" target=\"_blank\" rel=\"noopener noreferrer\"\u003e\n                        \u003ch3\u003eIntermolecular asymmetric functionalization of unstrained C(sp3)–C(sp3) bonds in allylic substitution reactions\u003c\/h3\u003e\n                    \u003c\/a\u003e\n                    \n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Name: Nature Synthesis\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Date: 2024-06-03\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003eDOI: 10.1038\/s44160-024-00555-z\u003c\/div\u003e\n                \n            \u003c\/div\u003e\n        \n            \u003cdiv class=\"reference-item\"\u003e\n                \n                    \n                    \u003ca href=\"https:\/\/science-of-synthesis.thieme.com\/app\/text\/?id=SD-120-00331\" target=\"_blank\" rel=\"noopener noreferrer\"\u003e\n                        \u003ch3\u003eCarboxylation of Alkyl Esters\u003c\/h3\u003e\n                    \u003c\/a\u003e\n                    \n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Name: Science of Synthesis\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Date: 2024\u003c\/div\u003e\n                \n\n                \n            \u003c\/div\u003e\n        \n            \u003cdiv class=\"reference-item\"\u003e\n                \n                    \n                    \u003ca href=\"https:\/\/doi.org\/10.1007\/s11426-023-1552-0\" target=\"_blank\" rel=\"noopener noreferrer\"\u003e\n                        \u003ch3\u003eCatalytic enantioselective domino alkenylation-alkynylation of alkenes: stereoselective synthesis of 5–7 membered azacycles and carbocycles\u003c\/h3\u003e\n                    \u003c\/a\u003e\n                    \n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Name: Science China Chemistry\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Date: 2023-04-10\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003eDOI: 10.1007\/s11426-023-1552-0\u003c\/div\u003e\n                \n            \u003c\/div\u003e\n        \n    \u003c\/div\u003e\n    \n\n\n    \u003cscript\u003e\n        const coaSearchButton = document.getElementById('coa-search-button');\n        coaSearchButton.addEventListener('click', async function() {\n            const coaLinkInput = 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#e0e0e0;\n    padding: 5px 8px;\n  }\n\n  @media (max-width: 600px) {\n    .section-row {\n      grid-template-columns: repeat(1, 1fr);\n    }\n\n    .section-row .row-key {\n      grid-column: 1 \/ 2;\n    }\n\n    .section-row .row-value {\n      grid-column: 1 \/ 2;\n    }\n\n    .hazard-grid {\n      grid-template-columns: repeat(2, 1fr);\n      gap: 0 20px;\n    }\n  }\n  \n\u003c\/style\u003e\n\n\u003cdiv class=\"section\"\u003e\n  \n\n    \u003c!-- Order Info --\u003e\n    \u003ch2 class=\"section-header\"\u003eProduct Information\u003c\/h2\u003e\n    \u003cdiv class=\"section-content\"\u003e\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eProduct Name\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e(S)-(-)-2,2'-Bis\u003cspan class=\"l_bracket\"\u003e\u003c\/span\u003edi(3,4,5-trimethoxyphenyl)phosphino\u003cspan class=\"r_bracket\"\u003e\u003c\/span\u003e-6,6'-dimethoxy-1,1'-biphenyl, min. 97%\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n        \n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eBrand Name\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003eUS-Strem\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eProduct Number\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e15-0159\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eCAS\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e927396-01-8\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n\n        \n\n        \n\n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eCertificate of Analysis (COA)​\u003c\/div\u003e\n            \u003cdiv 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stop-opacity=\"0\"\u003e\u003c\/stop\u003e\u003c\/radialgradient\u003e\u003ccircle transform-origin=\"center\" fill=\"none\" stroke=\"url(#a7)\" stroke-width=\"15\" stroke-linecap=\"round\" stroke-dasharray=\"200 1000\" stroke-dashoffset=\"0\" cx=\"100\" cy=\"100\" r=\"70\"\u003e\u003canimatetransform type=\"rotate\" attributename=\"transform\" calcmode=\"spline\" dur=\"2\" values=\"360;0\" keytimes=\"0;1\" keysplines=\"0 0 1 1\" repeatcount=\"indefinite\"\u003e\u003c\/animatetransform\u003e\u003c\/circle\u003e\u003ccircle transform-origin=\"center\" fill=\"none\" opacity=\".2\" stroke=\"#FFFFFF\" stroke-width=\"15\" stroke-linecap=\"round\" cx=\"100\" cy=\"100\" r=\"70\"\u003e\u003c\/circle\u003e\u003c\/svg\u003e\n                            \u003cspan\u003eSearch\u003c\/span\u003e\n                        \u003c\/div\u003e\n                    \u003c\/button\u003e\n                    \u003cspan class=\"coa-not-found\"\u003eCOA not found\u003c\/span\u003e\n                \u003c\/div\u003e\n            \u003c\/div\u003e\n        \u003c\/div\u003e\n\n    \u003c\/div\u003e\n\n    \u003c!-- General Info --\u003e\n    \n        \u003ch2 class=\"section-header\"\u003eGeneral Information\u003c\/h2\u003e\n        \u003cdiv class=\"section-content\"\u003e\n            \n\n            \n            \u003cdiv class=\"section-row\"\u003e\n                \u003cdiv class=\"row-key\"\u003ePubChem CID\u003c\/div\u003e\n                \u003cdiv class=\"row-value\"\u003e21806702\u003c\/div\u003e\n            \u003c\/div\u003e\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eIUPAC Name\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003e\n\u003cspan class=\"l_bracket\"\u003e\u003c\/span\u003e2-\u003cspan class=\"l_bracket\"\u003e\u003c\/span\u003e2-bis(3,4,5-trimethoxyphenyl)phosphanyl-6-methoxyphenyl\u003cspan class=\"r_bracket\"\u003e\u003c\/span\u003e-3-methoxyphenyl\u003cspan class=\"r_bracket\"\u003e\u003c\/span\u003e-bis(3,4,5-trimethoxyphenyl)phosphane\u003c\/div\u003e\n                \u003c\/div\u003e\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eInChI Key\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003eJZCMGMXFWZWFRX-UHFFFAOYSA-N\u003c\/div\u003e\n                \u003c\/div\u003e\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eSMILES\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003eCOC1=C(C(=CC=C1)P(C2=CC(=C(C(=C2)OC)OC)OC)C3=CC(=C(C(=C3)OC)OC)OC)C4=C(C=CC=C4P(C5=CC(=C(C(=C5)OC)OC)OC)C6=CC(=C(C(=C6)OC)OC)OC)OC\u003c\/div\u003e\n                \u003c\/div\u003e\n            \n        \u003c\/div\u003e\n    \n\n    \u003c!-- Properties --\u003e\n    \n\n    \u003c!-- Safety Info --\u003e\n    \n        \u003ch2 class=\"section-header\"\u003eSafety Information\u003c\/h2\u003e\n        \u003cdiv class=\"section-content\"\u003e\n            \n\n            \n\n            \n\n            \n\n            \n\n            \n\n            \n\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eStorage Condition\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003e\n                        Store at 2-8℃\n                    \u003c\/div\u003e\n                \u003c\/div\u003e\n            \n        \u003c\/div\u003e\n    \n\n    \u003c!-- Description --\u003e\n    \n    \u003ch2 class=\"section-header\"\u003eDescription\u003c\/h2\u003e\n    \u003cdiv class=\"html-area\"\u003e\n        Technical Notes:\u003cbr\u003e1.See 15-0042.\u003cbr\u003e2.Ru and Ir catalyzed dynamic kinetic resolution for the synthesis of hydroxy, amino acid derivatives. \r3.Ru-catalyzed asymmetric hydrogenation of ketones and alkenes .\u003cbr\u003e4.Ir catalyzed enantioselective hydrogenation of heteroaromatic compounds.\u003cbr\u003e5.Conjugate addition using 2-heteroaryl titanates and zinc reagents.\u003cbr\u003e6.Enantio- and regioselective heck-type reaction of aryl boronic acids with 2,3-dihydrofuran.\u003cbr\u003e7.Rhodium-catalyzed carbonyl Z-dienylation.\u003cbr\u003e8.Rhodium-catalyzed asymmetric 1 ,4 addition of arylboronic acids to maleimides and enones.\u003cbr\u003e9. Ligand for Rh-Catalyzed Asymmetric Hydrothiolation of Allenes with Aliphatic Thiols .\u003cbr\u003e10. Ligand for Rh-Catalyzed Asymmetric Conjugate Addition of Arylzinc Chlorides to Thiochromones .\n    \u003c\/div\u003e\n    \n\n    \u003c!-- Faq --\u003e\n    \n\n    \u003c!-- References --\u003e\n    \n    \u003ch2 class=\"section-header\"\u003e\n        \u003cspan style=\"display: block;\"\u003eReferences\u003c\/span\u003e\n        \u003cspan style=\"display: block; font-size: 1.2rem; color: #777; font-weight: lighter;\"\u003eData Source From Pubchem\u003c\/span\u003e\n    \u003c\/h2\u003e\n    \u003cdiv class=\"section-content\"\u003e\n        \n            \u003cdiv class=\"reference-item\"\u003e\n                \n                    \n                    \u003ca href=\"https:\/\/science-of-synthesis.thieme.com\/app\/text\/?id=SD-104-00838\" target=\"_blank\" rel=\"noopener noreferrer\"\u003e\n                        \u003ch3\u003eBy Reduction of Alkynyl Silyl Ketones\u003c\/h3\u003e\n                    \u003c\/a\u003e\n                    \n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Name: Science of Synthesis\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Date: 2022\u003c\/div\u003e\n                \n\n                \n            \u003c\/div\u003e\n        \n    \u003c\/div\u003e\n    \n\n\n    \u003cscript\u003e\n        const coaSearchButton = document.getElementById('coa-search-button');\n        coaSearchButton.addEventListener('click', async function() {\n            const coaLinkInput = document.getElementById('coa-link-input');\n            const spinElement = document.querySelector('.search-spin');\n            const notFoundElement = document.querySelector('.coa-not-found');\n\n            const lot = coaLinkInput.value.trim().toUpperCase();\n            if (lot.length \u003e 0) {\n                spinElement.style.display = 'block';\n                notFoundElement.style.display = 'none';\n\n            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#e0e0e0;\n    padding: 5px 8px;\n  }\n\n  @media (max-width: 600px) {\n    .section-row {\n      grid-template-columns: repeat(1, 1fr);\n    }\n\n    .section-row .row-key {\n      grid-column: 1 \/ 2;\n    }\n\n    .section-row .row-value {\n      grid-column: 1 \/ 2;\n    }\n\n    .hazard-grid {\n      grid-template-columns: repeat(2, 1fr);\n      gap: 0 20px;\n    }\n  }\n  \n\u003c\/style\u003e\n\n\u003cdiv class=\"section\"\u003e\n  \n\n    \u003c!-- Order Info --\u003e\n    \u003ch2 class=\"section-header\"\u003eProduct Information\u003c\/h2\u003e\n    \u003cdiv class=\"section-content\"\u003e\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eProduct Name\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e(S)-(-)-2,2'-Bis\u003cspan class=\"l_bracket\"\u003e\u003c\/span\u003edi(3,5-di-t-butylphenyl)phosphino\u003cspan class=\"r_bracket\"\u003e\u003c\/span\u003e-6,6'-dimethoxy-1,1'-biphenyl, min. 97%\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n        \n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eBrand Name\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003eUS-Strem\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eProduct Number\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e15-0045\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eCAS\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e167709-31-1\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n\n        \n\n        \n\n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eCertificate of Analysis (COA)​\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e\n                \u003cdiv class=\"coa-search-container\"\u003e\n                    \u003cinput id=\"coa-link-input\" type=\"text\" placeholder=\"Enter Lot No.\"\u003e\n                    \u003cbutton id=\"coa-search-button\"\u003e\n                        \u003cdiv class=\"coa-search-button-content\"\u003e\n                            \u003csvg class=\"search-spin\" xmlns=\"http:\/\/www.w3.org\/2000\/svg\" viewbox=\"0 0 200 200\"\u003e\u003cradialgradient id=\"a7\" cx=\".66\" fx=\".66\" cy=\".3125\" fy=\".3125\" gradienttransform=\"scale(1.5)\"\u003e\u003cstop offset=\"0\" stop-color=\"#FFFFFF\"\u003e\u003c\/stop\u003e\u003cstop offset=\".3\" stop-color=\"#FFFFFF\" stop-opacity=\".9\"\u003e\u003c\/stop\u003e\u003cstop offset=\".6\" stop-color=\"#FFFFFF\" stop-opacity=\".6\"\u003e\u003c\/stop\u003e\u003cstop offset=\".8\" stop-color=\"#FFFFFF\" stop-opacity=\".3\"\u003e\u003c\/stop\u003e\u003cstop offset=\"1\" stop-color=\"#FFFFFF\" stop-opacity=\"0\"\u003e\u003c\/stop\u003e\u003c\/radialgradient\u003e\u003ccircle transform-origin=\"center\" fill=\"none\" stroke=\"url(#a7)\" stroke-width=\"15\" stroke-linecap=\"round\" stroke-dasharray=\"200 1000\" stroke-dashoffset=\"0\" cx=\"100\" cy=\"100\" r=\"70\"\u003e\u003canimatetransform type=\"rotate\" attributename=\"transform\" calcmode=\"spline\" dur=\"2\" values=\"360;0\" keytimes=\"0;1\" keysplines=\"0 0 1 1\" repeatcount=\"indefinite\"\u003e\u003c\/animatetransform\u003e\u003c\/circle\u003e\u003ccircle transform-origin=\"center\" fill=\"none\" opacity=\".2\" stroke=\"#FFFFFF\" stroke-width=\"15\" stroke-linecap=\"round\" cx=\"100\" cy=\"100\" r=\"70\"\u003e\u003c\/circle\u003e\u003c\/svg\u003e\n                            \u003cspan\u003eSearch\u003c\/span\u003e\n                        \u003c\/div\u003e\n                    \u003c\/button\u003e\n                    \u003cspan class=\"coa-not-found\"\u003eCOA not found\u003c\/span\u003e\n                \u003c\/div\u003e\n            \u003c\/div\u003e\n        \u003c\/div\u003e\n\n    \u003c\/div\u003e\n\n    \u003c!-- General Info --\u003e\n    \n        \u003ch2 class=\"section-header\"\u003eGeneral Information\u003c\/h2\u003e\n        \u003cdiv class=\"section-content\"\u003e\n            \n\n            \n            \u003cdiv class=\"section-row\"\u003e\n                \u003cdiv class=\"row-key\"\u003ePubChem CID\u003c\/div\u003e\n                \u003cdiv class=\"row-value\"\u003e10964351\u003c\/div\u003e\n            \u003c\/div\u003e\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eIUPAC Name\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003e\n\u003cspan class=\"l_bracket\"\u003e\u003c\/span\u003e2-\u003cspan class=\"l_bracket\"\u003e\u003c\/span\u003e2-bis(3,5-ditert-butylphenyl)phosphanyl-6-methoxyphenyl\u003cspan class=\"r_bracket\"\u003e\u003c\/span\u003e-3-methoxyphenyl\u003cspan class=\"r_bracket\"\u003e\u003c\/span\u003e-bis(3,5-ditert-butylphenyl)phosphane\u003c\/div\u003e\n                \u003c\/div\u003e\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eInChI Key\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003ePBYRAYONARLAQJ-UHFFFAOYSA-N\u003c\/div\u003e\n                \u003c\/div\u003e\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eSMILES\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003eCC(C)(C)C1=CC(=CC(=C1)P(C2=CC=CC(=C2C3=C(C=CC=C3P(C4=CC(=CC(=C4)C(C)(C)C)C(C)(C)C)C5=CC(=CC(=C5)C(C)(C)C)C(C)(C)C)OC)OC)C6=CC(=CC(=C6)C(C)(C)C)C(C)(C)C)C(C)(C)C\u003c\/div\u003e\n                \u003c\/div\u003e\n            \n        \u003c\/div\u003e\n    \n\n    \u003c!-- Properties --\u003e\n    \n\n    \u003c!-- Safety Info --\u003e\n    \n\n    \u003c!-- Description --\u003e\n    \n    \u003ch2 class=\"section-header\"\u003eDescription\u003c\/h2\u003e\n    \u003cdiv class=\"html-area\"\u003e\n        Technical Notes:\u003cbr\u003e1.Ligand for the palladium-catalyzed intramolecular enantioselective allylic alkylation.\u003cbr\u003e2.Ligand for the palladium-catalyzed asymmetric synthesis of allenes at room temperature . \r3.Ligand for Rh- Catalyzed Asymmetric \u003cspan class=\"l_bracket\"\u003e\u003c\/span\u003e3+2\u003cspan class=\"r_bracket\"\u003e\u003c\/span\u003e Cycloaddition Reactions .\u003cbr\u003eReferences:\u003cbr\u003e1.Chem. Eur. J., 2011, 17, 2885.\u003cbr\u003e2.J. Am. Chem. Soc., 2013, 135, 11517. \r3.Angew. Chem. 2016, 128, 7892 7896.\n    \u003c\/div\u003e\n    \n\n    \u003c!-- Faq --\u003e\n    \n\n    \u003c!-- References --\u003e\n    \n    \u003ch2 class=\"section-header\"\u003e\n        \u003cspan style=\"display: block;\"\u003eReferences\u003c\/span\u003e\n        \u003cspan style=\"display: block; font-size: 1.2rem; color: #777; font-weight: lighter;\"\u003eData Source From Pubchem\u003c\/span\u003e\n    \u003c\/h2\u003e\n    \u003cdiv class=\"section-content\"\u003e\n        \n            \u003cdiv class=\"reference-item\"\u003e\n                \n                    \n                    \u003ca href=\"https:\/\/science-of-synthesis.thieme.com\/app\/text\/?id=SD-129-00237\" target=\"_blank\" rel=\"noopener noreferrer\"\u003e\n                        \u003ch3\u003eFunctionalization of 1,1-Difluoroalkenes\u003c\/h3\u003e\n                    \u003c\/a\u003e\n                    \n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Name: Science of Synthesis\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Date: 2025\u003c\/div\u003e\n                \n\n                \n            \u003c\/div\u003e\n        \n    \u003c\/div\u003e\n    \n\n\n    \u003cscript\u003e\n        const coaSearchButton = document.getElementById('coa-search-button');\n        coaSearchButton.addEventListener('click', async function() {\n            const coaLinkInput = document.getElementById('coa-link-input');\n            const spinElement = document.querySelector('.search-spin');\n            const notFoundElement = document.querySelector('.coa-not-found');\n\n            const lot = coaLinkInput.value.trim().toUpperCase();\n            if (lot.length \u003e 0) {\n                spinElement.style.display = 'block';\n                notFoundElement.style.display = 'none';\n\n                const url = `https:\/\/web.jkchemical.com\/partial\/coaFileLotNumber\/${lot}`;\n                await fetch(url).then((res) =\u003e {\n                    if (res.status === 200) {\n                        window.open(url, '_blank');\n                    } else {\n                        notFoundElement.style.display = 'block';\n                    }\n                }).finally(() =\u003e {\n                    spinElement.style.display = 'none';\n                });\n            }\n        });\n    \u003c\/script\u003e\n\n\n\u003c\/div\u003e","brand":"US-Strem","offers":[{"title":"1×10g","offer_id":45358200651966,"sku":"SC15-0045_10_G","price":4969.0,"currency_code":"USD","in_stock":true},{"title":"1×2g","offer_id":45358200684734,"sku":"SC15-0045_2_G","price":1244.0,"currency_code":"USD","in_stock":true},{"title":"1×100mg","offer_id":45358200717502,"sku":"SC15-0045_100_MG","price":99.0,"currency_code":"USD","in_stock":true},{"title":"1×500mg","offer_id":45358200750270,"sku":"SC15-0045_500_MG","price":366.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0506\/0005\/0878\/files\/6cf9006ec1656f11614cb020228a6649.jpg?v=1788908424"},{"product_id":"q8815-0043","title":"(S)-(+)-2,2'-Bis[di(3,5-di-t-butyl-4-methoxyphenyl)phosphino]-6,6'-dimethoxy-1,1'-biphenyl, min. 97% | 910134-30-4","description":"\u003cstyle\u003e\n  \/* isQuote *\/\n  div.swatch.clearfix {\n    display:  unset ;\n  }\n\n  \/* Hide sku *\/\n  .product-sku, \n  #leadtimetext {\n    display: none !important;\n  }\n\n  \/* Square brackets *\/\n  span.l_bracket:before {\n    content: \"[\";\n  }\n  span.r_bracket:after {\n    content: \"]\";\n  }\n\n  \/* Hazard Symbols *\/\n  .ghs-symbols-row {\n    display: flex;\n    flex-wrap: wrap;\n    gap: 10px;\n  }\n\n  .hazard-symbol-container {\n    width: 50px;\n  }\n\n  .hazard-symbol {\n    object-fit: contain;\n    aspect-ratio: 1 \/ 1;\n    width: 100%;\n  }\n\n  \/* Section *\/\n  .section-header {\n    font-size: 2rem;\n    font-weight: bold;\n    color: #239ab7;\n    background-color: #f2f2f2;\n    padding: 10px;\n    border-radius: 4px;\n  }\n\n  .section-row {\n    display: grid;\n    grid-template-columns: repeat(8, 1fr);\n    padding: 6px 10px;\n    border-bottom: 1px solid #e0e0e0;\n  }\n\n  .section-content {\n    padding-bottom: 6px;\n  }\n\n  .section-content .section-row:last-child {\n    border-bottom: none;\n  }\n\n  .section-row .row-key {\n    grid-column: 1 \/ 3;\n    font-weight: bold;\n    align-self: center;\n  }\n\n  .section-row .row-value {\n    grid-column: 3 \/ 9;\n  }\n\n  .section-row ul li {\n    line-height: 2rem !important;\n    font-size: 1.3rem;\n  }\n\n  .html-area {\n    padding: 10px;\n    width: 100%;\n    overflow-x: auto;\n  }\n\n  .html-area {\n    padding: 10px;\n  }\n\n  .html-area p {\n    margin: 0 !important;\n  }\n\n  .hazard-grid {\n    display: grid;\n    grid-template-columns: repeat(6, 1fr);\n    gap: 0 10px;\n    font-size: 1.3rem;\n  }\n\n  .reference-item {\n    padding: 10px 10px;\n    border-bottom: 1px solid #e0e0e0;\n  }\n\n  .section-content .reference-item:last-child {\n    border-bottom: none;\n  }\n\n  .reference-item h3 {\n    font-size: 1.5rem !important;\n  }\n\n  .reference-item .publication-item {\n    font-size: 1.3rem !important;\n    line-height: 1.5rem !important;\n  }\n\n  \/* SDS Search *\/\n  .section-row .coa-search-container {\n    display: flex;\n    align-items: center;\n    margin-top: 6px;\n  }\n\n  .section-row 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#e0e0e0;\n    padding: 5px 8px;\n  }\n\n  @media (max-width: 600px) {\n    .section-row {\n      grid-template-columns: repeat(1, 1fr);\n    }\n\n    .section-row .row-key {\n      grid-column: 1 \/ 2;\n    }\n\n    .section-row .row-value {\n      grid-column: 1 \/ 2;\n    }\n\n    .hazard-grid {\n      grid-template-columns: repeat(2, 1fr);\n      gap: 0 20px;\n    }\n  }\n  \n\u003c\/style\u003e\n\n\u003cdiv class=\"section\"\u003e\n  \n\n    \u003c!-- Order Info --\u003e\n    \u003ch2 class=\"section-header\"\u003eProduct Information\u003c\/h2\u003e\n    \u003cdiv class=\"section-content\"\u003e\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eProduct Name\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e(S)-(+)-2,2'-Bis\u003cspan class=\"l_bracket\"\u003e\u003c\/span\u003edi(3,5-di-t-butyl-4-methoxyphenyl)phosphino\u003cspan class=\"r_bracket\"\u003e\u003c\/span\u003e-6,6'-dimethoxy-1,1'-biphenyl, min. 97%\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n        \n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eBrand Name\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003eUS-Strem\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eProduct Number\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e15-0043\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eCAS\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e910134-30-4\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n\n        \n\n        \n\n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eCertificate of Analysis (COA)​\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e\n                \u003cdiv class=\"coa-search-container\"\u003e\n                    \u003cinput id=\"coa-link-input\" type=\"text\" placeholder=\"Enter Lot No.\"\u003e\n                    \u003cbutton id=\"coa-search-button\"\u003e\n                        \u003cdiv class=\"coa-search-button-content\"\u003e\n                            \u003csvg class=\"search-spin\" xmlns=\"http:\/\/www.w3.org\/2000\/svg\" viewbox=\"0 0 200 200\"\u003e\u003cradialgradient id=\"a7\" cx=\".66\" fx=\".66\" cy=\".3125\" fy=\".3125\" gradienttransform=\"scale(1.5)\"\u003e\u003cstop offset=\"0\" stop-color=\"#FFFFFF\"\u003e\u003c\/stop\u003e\u003cstop offset=\".3\" stop-color=\"#FFFFFF\" stop-opacity=\".9\"\u003e\u003c\/stop\u003e\u003cstop offset=\".6\" stop-color=\"#FFFFFF\" stop-opacity=\".6\"\u003e\u003c\/stop\u003e\u003cstop offset=\".8\" stop-color=\"#FFFFFF\" stop-opacity=\".3\"\u003e\u003c\/stop\u003e\u003cstop offset=\"1\" stop-color=\"#FFFFFF\" stop-opacity=\"0\"\u003e\u003c\/stop\u003e\u003c\/radialgradient\u003e\u003ccircle transform-origin=\"center\" fill=\"none\" stroke=\"url(#a7)\" stroke-width=\"15\" stroke-linecap=\"round\" stroke-dasharray=\"200 1000\" stroke-dashoffset=\"0\" cx=\"100\" cy=\"100\" r=\"70\"\u003e\u003canimatetransform type=\"rotate\" attributename=\"transform\" calcmode=\"spline\" dur=\"2\" values=\"360;0\" keytimes=\"0;1\" keysplines=\"0 0 1 1\" repeatcount=\"indefinite\"\u003e\u003c\/animatetransform\u003e\u003c\/circle\u003e\u003ccircle transform-origin=\"center\" fill=\"none\" opacity=\".2\" stroke=\"#FFFFFF\" stroke-width=\"15\" stroke-linecap=\"round\" cx=\"100\" cy=\"100\" r=\"70\"\u003e\u003c\/circle\u003e\u003c\/svg\u003e\n                            \u003cspan\u003eSearch\u003c\/span\u003e\n                        \u003c\/div\u003e\n                    \u003c\/button\u003e\n                    \u003cspan class=\"coa-not-found\"\u003eCOA not found\u003c\/span\u003e\n                \u003c\/div\u003e\n            \u003c\/div\u003e\n        \u003c\/div\u003e\n\n    \u003c\/div\u003e\n\n    \u003c!-- General Info --\u003e\n    \n        \u003ch2 class=\"section-header\"\u003eGeneral Information\u003c\/h2\u003e\n        \u003cdiv class=\"section-content\"\u003e\n            \n\n            \n            \u003cdiv class=\"section-row\"\u003e\n                \u003cdiv class=\"row-key\"\u003ePubChem CID\u003c\/div\u003e\n                \u003cdiv class=\"row-value\"\u003e11378383\u003c\/div\u003e\n            \u003c\/div\u003e\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eIUPAC Name\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003e\n\u003cspan class=\"l_bracket\"\u003e\u003c\/span\u003e2-\u003cspan class=\"l_bracket\"\u003e\u003c\/span\u003e2-bis(3,5-ditert-butyl-4-methoxyphenyl)phosphanyl-6-methoxyphenyl\u003cspan class=\"r_bracket\"\u003e\u003c\/span\u003e-3-methoxyphenyl\u003cspan class=\"r_bracket\"\u003e\u003c\/span\u003e-bis(3,5-ditert-butyl-4-methoxyphenyl)phosphane\u003c\/div\u003e\n                \u003c\/div\u003e\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eInChI Key\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003eJSSIQFXOSWLAGA-UHFFFAOYSA-N\u003c\/div\u003e\n                \u003c\/div\u003e\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eSMILES\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003eCC(C)(C)C1=CC(=CC(=C1OC)C(C)(C)C)P(C2=CC=CC(=C2C3=C(C=CC=C3P(C4=CC(=C(C(=C4)C(C)(C)C)OC)C(C)(C)C)C5=CC(=C(C(=C5)C(C)(C)C)OC)C(C)(C)C)OC)OC)C6=CC(=C(C(=C6)C(C)(C)C)OC)C(C)(C)C\u003c\/div\u003e\n                \u003c\/div\u003e\n            \n        \u003c\/div\u003e\n    \n\n    \u003c!-- Properties --\u003e\n    \n\n    \u003c!-- Safety Info --\u003e\n    \n\n    \u003c!-- Description --\u003e\n    \n    \u003ch2 class=\"section-header\"\u003eDescription\u003c\/h2\u003e\n    \u003cdiv class=\"html-area\"\u003e\n        Technical Notes:\u003cbr\u003e1.Ligand for asymmetric Rh-catalyzed Pausan-Khand reaction .\u003cbr\u003e2.Ligand for enantioselective Rh- catalyzed \u003cspan class=\"l_bracket\"\u003e\u003c\/span\u003e3 +2\u003cspan class=\"r_bracket\"\u003e\u003c\/span\u003e annulation of aromatic ketimines.\u003cbr\u003e3.Ligand for enantioselective copper-organocatalyzed preparation of cyclopentanes bearing an all-carbon\u003cbr\u003equaternary stereocenters.\u003cbr\u003e4.Ligand for Cu(l)-catalyzed exo- selective construction of spiro-\u003cspan class=\"l_bracket\"\u003e\u003c\/span\u003ebutyrolactonepyrrolidine\u003cspan class=\"r_bracket\"\u003e\u003c\/span\u003e via 1 ,3-dipolar cycloaddition of azomethine.\u003cbr\u003e5.Ligand for gold-catalyzed enantioselective intramolecular hydroamination of unactivated alkenes.\u003cbr\u003e6.Ligand for rhodium-catalyzed enantioselective intramolecular c -H silylation for the syntheses of planar-chiral metallocene siloles.\u003cbr\u003e7.Ligand for palladium-catalyzed enantioselective intermolecular carboetherification of dihydrofurans.\u003cbr\u003e8.Copper(I)-catalyzed asymmetric exo-selective \u003cspan class=\"l_bracket\"\u003e\u003c\/span\u003e3+ 2\u003cspan class=\"r_bracket\"\u003e\u003c\/span\u003e cycloaddition of azomethine ylides with ß-trifluoromethyl ß, ß-disubstituted enones.\u003cbr\u003e9.Ligand for Cu-Catalyzed Asymmetric Conjugate Alkynylation of a,ß-Unsaturated 1,1,1-Trifluoromethyl\u003cbr\u003eKetones with Terminal Alkynes\u003cbr\u003e10. L igand for Rhodium-Catalyzed Asymmetric N-H Functionalization of Quinazolinones with Allylic Carbonates\n    \u003c\/div\u003e\n    \n\n    \u003c!-- Faq --\u003e\n    \n\n    \u003c!-- References --\u003e\n    \n    \u003ch2 class=\"section-header\"\u003e\n        \u003cspan style=\"display: block;\"\u003eReferences\u003c\/span\u003e\n        \u003cspan style=\"display: block; font-size: 1.2rem; color: #777; font-weight: lighter;\"\u003eData Source From Pubchem\u003c\/span\u003e\n    \u003c\/h2\u003e\n    \u003cdiv class=\"section-content\"\u003e\n        \n            \u003cdiv class=\"reference-item\"\u003e\n                \n                    \n                    \u003ca href=\"https:\/\/science-of-synthesis.thieme.com\/app\/text\/?id=SD-147-00237\" target=\"_blank\" rel=\"noopener noreferrer\"\u003e\n                        \u003ch3\u003eEnantioselective Addition of Pyridin-2(1H)-ones to Terminal Allenes\u003c\/h3\u003e\n                    \u003c\/a\u003e\n                    \n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Name: Science of Synthesis\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Date: 2023\u003c\/div\u003e\n                \n\n                \n            \u003c\/div\u003e\n        \n            \u003cdiv class=\"reference-item\"\u003e\n                \n                    \n                    \u003ca href=\"https:\/\/science-of-synthesis.thieme.com\/app\/text\/?id=SD-237-00123\" target=\"_blank\" rel=\"noopener noreferrer\"\u003e\n                        \u003ch3\u003eDKR Hydrogenations\u003c\/h3\u003e\n                    \u003c\/a\u003e\n                    \n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Name: Science of Synthesis\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Date: 2022\u003c\/div\u003e\n                \n\n                \n            \u003c\/div\u003e\n        \n            \u003cdiv class=\"reference-item\"\u003e\n                \n                    \n                    \u003ca href=\"https:\/\/science-of-synthesis.thieme.com\/app\/text\/?id=SD-237-00158\" target=\"_blank\" rel=\"noopener noreferrer\"\u003e\n                        \u003ch3\u003eRacemic α-Substituted Imines\u003c\/h3\u003e\n                    \u003c\/a\u003e\n                    \n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Name: Science of Synthesis\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Date: 2022\u003c\/div\u003e\n                \n\n                \n            \u003c\/div\u003e\n        \n            \u003cdiv class=\"reference-item\"\u003e\n                \n                    \n                    \u003ca href=\"https:\/\/science-of-synthesis.thieme.com\/app\/text\/?id=SD-221-00080\" target=\"_blank\" rel=\"noopener noreferrer\"\u003e\n                        \u003ch3\u003eGold Catalysis\u003c\/h3\u003e\n                    \u003c\/a\u003e\n                    \n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Name: Science of Synthesis\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Date: 2016\u003c\/div\u003e\n                \n\n                \n            \u003c\/div\u003e\n        \n            \u003cdiv class=\"reference-item\"\u003e\n                \n                    \n                    \u003ca href=\"https:\/\/doi.org\/10.1007\/7081_2015_5003\" target=\"_blank\" rel=\"noopener noreferrer\"\u003e\n                        \u003ch3\u003eEnantioselective Gold-Catalyzed Synthesis of Heterocyclic Compounds\u003c\/h3\u003e\n                    \u003c\/a\u003e\n                    \n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Name: Au-Catalyzed Synthesis and Functionalization of Heterocycles\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Date: 2015\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003eDOI: 10.1007\/7081_2015_5003\u003c\/div\u003e\n                \n            \u003c\/div\u003e\n        \n    \u003c\/div\u003e\n    \n\n\n    \u003cscript\u003e\n        const coaSearchButton = document.getElementById('coa-search-button');\n        coaSearchButton.addEventListener('click', async function() {\n            const coaLinkInput = document.getElementById('coa-link-input');\n            const spinElement = document.querySelector('.search-spin');\n            const notFoundElement = document.querySelector('.coa-not-found');\n\n            const lot = coaLinkInput.value.trim().toUpperCase();\n            if (lot.length \u003e 0) {\n                spinElement.style.display = 'block';\n                notFoundElement.style.display = 'none';\n\n                const url = `https:\/\/web.jkchemical.com\/partial\/coaFileLotNumber\/${lot}`;\n                await fetch(url).then((res) =\u003e {\n                    if (res.status === 200) {\n                        window.open(url, '_blank');\n                    } else {\n                        notFoundElement.style.display = 'block';\n                    }\n                }).finally(() =\u003e {\n                    spinElement.style.display = 'none';\n                });\n            }\n        });\n    \u003c\/script\u003e\n\n\n\u003c\/div\u003e","brand":"US-Strem","offers":[{"title":"1×2g","offer_id":45358201864382,"sku":"SC15-0043_2_G","price":1244.0,"currency_code":"USD","in_stock":true},{"title":"1×10g","offer_id":45358201897150,"sku":"SC15-0043_10_G","price":4969.0,"currency_code":"USD","in_stock":true},{"title":"1×100mg","offer_id":45358201929918,"sku":"SC15-0043_100_MG","price":99.0,"currency_code":"USD","in_stock":true},{"title":"1×500mg","offer_id":45358201962686,"sku":"SC15-0043_500_MG","price":366.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0506\/0005\/0878\/files\/2b5c6fc02147cd7a657bc18bcf92c95a.jpg?v=1788908424"},{"product_id":"q8815-0044","title":"(R)-(+)-2,2'-Bis[di(3,5-di-t-butylphenyl)phosphino]-6,6'-dimethoxy-1,1'-biphenyl, min. 97% | 192138-05-9","description":"\u003cstyle\u003e\n  \/* isQuote *\/\n  div.swatch.clearfix {\n    display:  unset ;\n  }\n\n  \/* Hide sku *\/\n  .product-sku, \n  #leadtimetext {\n    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#e0e0e0;\n    padding: 5px 8px;\n  }\n\n  @media (max-width: 600px) {\n    .section-row {\n      grid-template-columns: repeat(1, 1fr);\n    }\n\n    .section-row .row-key {\n      grid-column: 1 \/ 2;\n    }\n\n    .section-row .row-value {\n      grid-column: 1 \/ 2;\n    }\n\n    .hazard-grid {\n      grid-template-columns: repeat(2, 1fr);\n      gap: 0 20px;\n    }\n  }\n  \n\u003c\/style\u003e\n\n\u003cdiv class=\"section\"\u003e\n  \n\n    \u003c!-- Order Info --\u003e\n    \u003ch2 class=\"section-header\"\u003eProduct Information\u003c\/h2\u003e\n    \u003cdiv class=\"section-content\"\u003e\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eProduct Name\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e(R)-(+)-2,2'-Bis\u003cspan class=\"l_bracket\"\u003e\u003c\/span\u003edi(3,5-di-t-butylphenyl)phosphino\u003cspan class=\"r_bracket\"\u003e\u003c\/span\u003e-6,6'-dimethoxy-1,1'-biphenyl, min. 97%\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n        \n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eBrand Name\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003eUS-Strem\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eProduct Number\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e15-0044\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eCAS\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e192138-05-9\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n\n        \n\n        \n\n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eCertificate of Analysis (COA)​\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e\n                \u003cdiv class=\"coa-search-container\"\u003e\n                    \u003cinput id=\"coa-link-input\" type=\"text\" placeholder=\"Enter Lot No.\"\u003e\n                    \u003cbutton id=\"coa-search-button\"\u003e\n                        \u003cdiv class=\"coa-search-button-content\"\u003e\n                            \u003csvg class=\"search-spin\" xmlns=\"http:\/\/www.w3.org\/2000\/svg\" viewbox=\"0 0 200 200\"\u003e\u003cradialgradient id=\"a7\" cx=\".66\" fx=\".66\" cy=\".3125\" fy=\".3125\" gradienttransform=\"scale(1.5)\"\u003e\u003cstop offset=\"0\" stop-color=\"#FFFFFF\"\u003e\u003c\/stop\u003e\u003cstop offset=\".3\" stop-color=\"#FFFFFF\" stop-opacity=\".9\"\u003e\u003c\/stop\u003e\u003cstop offset=\".6\" stop-color=\"#FFFFFF\" stop-opacity=\".6\"\u003e\u003c\/stop\u003e\u003cstop offset=\".8\" stop-color=\"#FFFFFF\" stop-opacity=\".3\"\u003e\u003c\/stop\u003e\u003cstop offset=\"1\" stop-color=\"#FFFFFF\" stop-opacity=\"0\"\u003e\u003c\/stop\u003e\u003c\/radialgradient\u003e\u003ccircle transform-origin=\"center\" fill=\"none\" stroke=\"url(#a7)\" stroke-width=\"15\" stroke-linecap=\"round\" stroke-dasharray=\"200 1000\" stroke-dashoffset=\"0\" cx=\"100\" cy=\"100\" r=\"70\"\u003e\u003canimatetransform type=\"rotate\" attributename=\"transform\" calcmode=\"spline\" dur=\"2\" values=\"360;0\" keytimes=\"0;1\" keysplines=\"0 0 1 1\" repeatcount=\"indefinite\"\u003e\u003c\/animatetransform\u003e\u003c\/circle\u003e\u003ccircle transform-origin=\"center\" fill=\"none\" opacity=\".2\" stroke=\"#FFFFFF\" stroke-width=\"15\" stroke-linecap=\"round\" cx=\"100\" cy=\"100\" r=\"70\"\u003e\u003c\/circle\u003e\u003c\/svg\u003e\n                            \u003cspan\u003eSearch\u003c\/span\u003e\n                        \u003c\/div\u003e\n                    \u003c\/button\u003e\n                    \u003cspan class=\"coa-not-found\"\u003eCOA not found\u003c\/span\u003e\n                \u003c\/div\u003e\n            \u003c\/div\u003e\n        \u003c\/div\u003e\n\n    \u003c\/div\u003e\n\n    \u003c!-- General Info --\u003e\n    \n        \u003ch2 class=\"section-header\"\u003eGeneral Information\u003c\/h2\u003e\n        \u003cdiv class=\"section-content\"\u003e\n            \n\n            \n            \u003cdiv class=\"section-row\"\u003e\n                \u003cdiv class=\"row-key\"\u003ePubChem CID\u003c\/div\u003e\n                \u003cdiv class=\"row-value\"\u003e10964351\u003c\/div\u003e\n            \u003c\/div\u003e\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eIUPAC Name\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003e\n\u003cspan class=\"l_bracket\"\u003e\u003c\/span\u003e2-\u003cspan class=\"l_bracket\"\u003e\u003c\/span\u003e2-bis(3,5-ditert-butylphenyl)phosphanyl-6-methoxyphenyl\u003cspan class=\"r_bracket\"\u003e\u003c\/span\u003e-3-methoxyphenyl\u003cspan class=\"r_bracket\"\u003e\u003c\/span\u003e-bis(3,5-ditert-butylphenyl)phosphane\u003c\/div\u003e\n                \u003c\/div\u003e\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eInChI Key\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003ePBYRAYONARLAQJ-UHFFFAOYSA-N\u003c\/div\u003e\n                \u003c\/div\u003e\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eSMILES\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003eCC(C)(C)C1=CC(=CC(=C1)P(C2=CC=CC(=C2C3=C(C=CC=C3P(C4=CC(=CC(=C4)C(C)(C)C)C(C)(C)C)C5=CC(=CC(=C5)C(C)(C)C)C(C)(C)C)OC)OC)C6=CC(=CC(=C6)C(C)(C)C)C(C)(C)C)C(C)(C)C\u003c\/div\u003e\n                \u003c\/div\u003e\n            \n        \u003c\/div\u003e\n    \n\n    \u003c!-- Properties --\u003e\n    \n\n    \u003c!-- Safety Info --\u003e\n    \n\n    \u003c!-- Description --\u003e\n    \n    \u003ch2 class=\"section-header\"\u003eDescription\u003c\/h2\u003e\n    \u003cdiv class=\"html-area\"\u003e\n        Technical Notes:\u003cbr\u003e1.Ligand for the highly enantioselective, rhodium-catalyzed \u003cspan class=\"l_bracket\"\u003e\u003c\/span\u003e2 +2+2\u003cspan class=\"r_bracket\"\u003e\u003c\/span\u003e cycloaddition of diynes to sulfonimines . \r2. Ligand for asymmetric gold-catalyzed lactonizations in water at room temperature .\u003cbr\u003e3. Ligand for Rh- Catalyzed Asymmetric \u003cspan class=\"l_bracket\"\u003e\u003c\/span\u003e3+2\u003cspan class=\"r_bracket\"\u003e\u003c\/span\u003e Cycloaddition Reactions.\u003cbr\u003eReferences:\u003cbr\u003e1.J. Am. Chem. Soc., 2013, 135, 4576.\u003cbr\u003e2.Angew. Chem. Int. Ed., 2014, 53, 1 0658. \r3Angew. Chem. 2016, 128, 7892 7896.\n    \u003c\/div\u003e\n    \n\n    \u003c!-- Faq --\u003e\n    \n\n    \u003c!-- References --\u003e\n    \n    \u003ch2 class=\"section-header\"\u003e\n        \u003cspan style=\"display: block;\"\u003eReferences\u003c\/span\u003e\n        \u003cspan style=\"display: block; font-size: 1.2rem; color: #777; font-weight: lighter;\"\u003eData Source From Pubchem\u003c\/span\u003e\n    \u003c\/h2\u003e\n    \u003cdiv class=\"section-content\"\u003e\n        \n            \u003cdiv class=\"reference-item\"\u003e\n                \n                    \n                    \u003ca href=\"https:\/\/science-of-synthesis.thieme.com\/app\/text\/?id=SD-129-00237\" target=\"_blank\" rel=\"noopener noreferrer\"\u003e\n                        \u003ch3\u003eFunctionalization of 1,1-Difluoroalkenes\u003c\/h3\u003e\n                    \u003c\/a\u003e\n                    \n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Name: Science of Synthesis\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Date: 2025\u003c\/div\u003e\n                \n\n                \n            \u003c\/div\u003e\n        \n    \u003c\/div\u003e\n    \n\n\n    \u003cscript\u003e\n        const coaSearchButton = document.getElementById('coa-search-button');\n        coaSearchButton.addEventListener('click', async function() {\n            const coaLinkInput = document.getElementById('coa-link-input');\n            const spinElement = document.querySelector('.search-spin');\n            const notFoundElement = document.querySelector('.coa-not-found');\n\n            const lot = coaLinkInput.value.trim().toUpperCase();\n            if (lot.length \u003e 0) {\n                spinElement.style.display = 'block';\n                notFoundElement.style.display = 'none';\n\n                const url = 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class=\"row-key\"\u003eBrand Name\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003eUS-Strem\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eProduct Number\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e15-0112\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eCAS\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e145214-57-9\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n\n        \n\n        \n\n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eCertificate of Analysis (COA)​\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e\n                \u003cdiv class=\"coa-search-container\"\u003e\n                    \u003cinput id=\"coa-link-input\" 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stroke-linecap=\"round\" stroke-dasharray=\"200 1000\" stroke-dashoffset=\"0\" cx=\"100\" cy=\"100\" r=\"70\"\u003e\u003canimatetransform type=\"rotate\" attributename=\"transform\" calcmode=\"spline\" dur=\"2\" values=\"360;0\" keytimes=\"0;1\" keysplines=\"0 0 1 1\" repeatcount=\"indefinite\"\u003e\u003c\/animatetransform\u003e\u003c\/circle\u003e\u003ccircle transform-origin=\"center\" fill=\"none\" opacity=\".2\" stroke=\"#FFFFFF\" stroke-width=\"15\" stroke-linecap=\"round\" cx=\"100\" cy=\"100\" r=\"70\"\u003e\u003c\/circle\u003e\u003c\/svg\u003e\n                            \u003cspan\u003eSearch\u003c\/span\u003e\n                        \u003c\/div\u003e\n                    \u003c\/button\u003e\n                    \u003cspan class=\"coa-not-found\"\u003eCOA not found\u003c\/span\u003e\n                \u003c\/div\u003e\n            \u003c\/div\u003e\n        \u003c\/div\u003e\n\n    \u003c\/div\u003e\n\n    \u003c!-- General Info --\u003e\n    \n        \u003ch2 class=\"section-header\"\u003eGeneral Information\u003c\/h2\u003e\n        \u003cdiv class=\"section-content\"\u003e\n            \n\n            \n            \u003cdiv class=\"section-row\"\u003e\n                \u003cdiv class=\"row-key\"\u003ePubChem CID\u003c\/div\u003e\n                \u003cdiv class=\"row-value\"\u003e15307805\u003c\/div\u003e\n            \u003c\/div\u003e\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eIUPAC Name\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003e\n\u003cspan class=\"l_bracket\"\u003e\u003c\/span\u003e2-\u003cspan class=\"l_bracket\"\u003e\u003c\/span\u003e2-\u003cspan class=\"l_bracket\"\u003e\u003c\/span\u003ebis(furan-2-yl)phosphanyl\u003cspan class=\"r_bracket\"\u003e\u003c\/span\u003e-6-methoxyphenyl\u003cspan class=\"r_bracket\"\u003e\u003c\/span\u003e-3-methoxyphenyl\u003cspan class=\"r_bracket\"\u003e\u003c\/span\u003e-bis(furan-2-yl)phosphane\u003c\/div\u003e\n                \u003c\/div\u003e\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eInChI Key\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003eABGYJVGTLXSMBM-UHFFFAOYSA-N\u003c\/div\u003e\n                \u003c\/div\u003e\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eSMILES\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003eCOC1=C(C(=CC=C1)P(C2=CC=CO2)C3=CC=CO3)C4=C(C=CC=C4P(C5=CC=CO5)C6=CC=CO6)OC\u003c\/div\u003e\n                \u003c\/div\u003e\n            \n        \u003c\/div\u003e\n    \n\n    \u003c!-- Properties --\u003e\n    \n\n    \u003c!-- Safety Info --\u003e\n    \n        \u003ch2 class=\"section-header\"\u003eSafety Information\u003c\/h2\u003e\n        \u003cdiv class=\"section-content\"\u003e\n            \n\n            \n\n            \n\n            \n\n            \n\n            \n\n            \n\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eStorage Condition\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003e\n                        Store at 2-8℃\n                    \u003c\/div\u003e\n                \u003c\/div\u003e\n            \n        \u003c\/div\u003e\n    \n\n    \u003c!-- Description --\u003e\n    \n    \u003ch2 class=\"section-header\"\u003eDescription\u003c\/h2\u003e\n    \u003cdiv class=\"html-area\"\u003e\n        Technical Notes:\u003cbr\u003e1. Cu-catalyzed diastereo- and enantioselective reactions of bis(pinacolato)diboron 1,3-enynes and aldehydes. \r2. Ru-catalyzed enantioselective, hydroaminomethylation of dienes and isoprene with 1 ,3 , 5-tris(aryl)-hexahydro-1 ,3,5-triazines .\u003cbr\u003e3. Ir-catalyzed asymmetric hydrogenation of quinoxaline-2-carboxylates .\u003cbr\u003eReferences:\u003cbr\u003e1. J. Am. Chem. Soc., 2014, 136, 11304. \r2. Chem. Sci., 2016, 7, 136.\u003cbr\u003e3. Tetrahedron, 2016, 72, 1375.\n    \u003c\/div\u003e\n    \n\n    \u003c!-- Faq --\u003e\n    \n\n    \u003c!-- References --\u003e\n    \n    \u003ch2 class=\"section-header\"\u003e\n        \u003cspan style=\"display: block;\"\u003eReferences\u003c\/span\u003e\n        \u003cspan style=\"display: block; font-size: 1.2rem; color: #777; font-weight: lighter;\"\u003eData Source From Pubchem\u003c\/span\u003e\n    \u003c\/h2\u003e\n    \u003cdiv class=\"section-content\"\u003e\n        \n            \u003cdiv class=\"reference-item\"\u003e\n                \n                    \n                    \u003ca href=\"https:\/\/doi.org\/10.1055\/s-0040-1707160\" target=\"_blank\" rel=\"noopener noreferrer\"\u003e\n                        \u003ch3\u003eRecent Advances of 1,3,5-Triazinanes in Aminomethylation and Cycloaddition Reactions\u003c\/h3\u003e\n                    \u003c\/a\u003e\n                    \n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Name: Synthesis\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Date: 2020-07-06\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003eDOI: 10.1055\/s-0040-1707160\u003c\/div\u003e\n                \n            \u003c\/div\u003e\n        \n            \u003cdiv class=\"reference-item\"\u003e\n                \n                    \n                    \u003ca href=\"https:\/\/doi.org\/10.1055\/s-0039-1690490\" target=\"_blank\" rel=\"noopener noreferrer\"\u003e\n                        \u003ch3\u003eSynthesis of a CGRP Receptor Antagonist\u003c\/h3\u003e\n                    \u003c\/a\u003e\n                    \n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Name: Synfacts\u003c\/div\u003e\n                \n\n                \n                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6px;\n  }\n\n  .section-row .coa-search-container input {\n    border: 1px solid #e0e0e0;\n    height: 2.5rem;\n    border-top-left-radius: 0.5rem !important;\n    border-bottom-left-radius: 0.5rem !important;\n    padding: 3px 5px;\n  }\n\n  .section-row .coa-search-container button {\n    height: 2.5rem;\n    line-height: 2.5rem;\n    border-radius: 0 0.5rem 0.5rem 0;\n  }\n\n  .section-row .coa-search-container button .coa-search-button-content {\n    display: flex;\n    align-items: center;\n    justify-content: center;\n    gap: 3px;\n  }\n\n  .section-row .coa-search-container button .coa-search-button-content .search-spin {\n    display: none;\n    width: 2rem;\n  }\n\n  .section-row .coa-search-container .coa-not-found {\n    display: none;\n    margin: 0 0 0 2rem;\n    color: #ad2031;\n    font-size: 1.3rem;\n  }\n\n  \/* Table *\/\n  .html-area table {\n    width: 100%;\n    border-collapse: collapse;\n    margin: 15px 0;\n  }\n\n  .html-area table th,\n  .html-area table td {\n    border: 1px solid #e0e0e0;\n    padding: 5px 8px;\n  }\n\n  @media (max-width: 600px) {\n    .section-row {\n      grid-template-columns: repeat(1, 1fr);\n    }\n\n    .section-row .row-key {\n      grid-column: 1 \/ 2;\n    }\n\n    .section-row .row-value {\n      grid-column: 1 \/ 2;\n    }\n\n    .hazard-grid {\n      grid-template-columns: repeat(2, 1fr);\n      gap: 0 20px;\n    }\n  }\n  \n\u003c\/style\u003e\n\n\u003cdiv class=\"section\"\u003e\n  \n\n    \u003c!-- Order Info --\u003e\n    \u003ch2 class=\"section-header\"\u003eProduct Information\u003c\/h2\u003e\n    \u003cdiv class=\"section-content\"\u003e\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eProduct Name\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e(S)-(-)-5,5'-Dichloro-6,6'-dimethoxy-2,2'-bis(diphenyl­phosphino)-1,1'-biphenyl, min. 95% (S)-Cl-MeO-BIPHEP\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n        \n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eBrand Name\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003eUS-Strem\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eProduct Number\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e15-1056\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eCAS\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e185913-98-8\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n\n        \n\n        \n\n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eCertificate of Analysis (COA)​\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e\n                \u003cdiv class=\"coa-search-container\"\u003e\n                    \u003cinput id=\"coa-link-input\" type=\"text\" placeholder=\"Enter Lot No.\"\u003e\n                    \u003cbutton id=\"coa-search-button\"\u003e\n                        \u003cdiv class=\"coa-search-button-content\"\u003e\n                            \u003csvg class=\"search-spin\" xmlns=\"http:\/\/www.w3.org\/2000\/svg\" viewbox=\"0 0 200 200\"\u003e\u003cradialgradient id=\"a7\" cx=\".66\" fx=\".66\" cy=\".3125\" fy=\".3125\" gradienttransform=\"scale(1.5)\"\u003e\u003cstop offset=\"0\" stop-color=\"#FFFFFF\"\u003e\u003c\/stop\u003e\u003cstop offset=\".3\" stop-color=\"#FFFFFF\" stop-opacity=\".9\"\u003e\u003c\/stop\u003e\u003cstop offset=\".6\" stop-color=\"#FFFFFF\" stop-opacity=\".6\"\u003e\u003c\/stop\u003e\u003cstop offset=\".8\" stop-color=\"#FFFFFF\" stop-opacity=\".3\"\u003e\u003c\/stop\u003e\u003cstop offset=\"1\" stop-color=\"#FFFFFF\" stop-opacity=\"0\"\u003e\u003c\/stop\u003e\u003c\/radialgradient\u003e\u003ccircle transform-origin=\"center\" fill=\"none\" stroke=\"url(#a7)\" stroke-width=\"15\" stroke-linecap=\"round\" stroke-dasharray=\"200 1000\" stroke-dashoffset=\"0\" cx=\"100\" cy=\"100\" r=\"70\"\u003e\u003canimatetransform type=\"rotate\" attributename=\"transform\" calcmode=\"spline\" dur=\"2\" values=\"360;0\" keytimes=\"0;1\" keysplines=\"0 0 1 1\" repeatcount=\"indefinite\"\u003e\u003c\/animatetransform\u003e\u003c\/circle\u003e\u003ccircle transform-origin=\"center\" fill=\"none\" opacity=\".2\" stroke=\"#FFFFFF\" stroke-width=\"15\" stroke-linecap=\"round\" cx=\"100\" cy=\"100\" r=\"70\"\u003e\u003c\/circle\u003e\u003c\/svg\u003e\n                            \u003cspan\u003eSearch\u003c\/span\u003e\n                        \u003c\/div\u003e\n                    \u003c\/button\u003e\n                    \u003cspan class=\"coa-not-found\"\u003eCOA not found\u003c\/span\u003e\n                \u003c\/div\u003e\n            \u003c\/div\u003e\n        \u003c\/div\u003e\n\n    \u003c\/div\u003e\n\n    \u003c!-- General Info --\u003e\n    \n        \u003ch2 class=\"section-header\"\u003eGeneral Information\u003c\/h2\u003e\n        \u003cdiv class=\"section-content\"\u003e\n            \n\n            \n            \u003cdiv class=\"section-row\"\u003e\n                \u003cdiv class=\"row-key\"\u003ePubChem CID\u003c\/div\u003e\n                \u003cdiv class=\"row-value\"\u003e5165044\u003c\/div\u003e\n            \u003c\/div\u003e\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eIUPAC Name\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003e\n\u003cspan class=\"l_bracket\"\u003e\u003c\/span\u003e4-chloro-2-(3-chloro-6-diphenylphosphanyl-2-methoxyphenyl)-3-methoxyphenyl\u003cspan class=\"r_bracket\"\u003e\u003c\/span\u003e-diphenylphosphane\u003c\/div\u003e\n                \u003c\/div\u003e\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eInChI Key\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003eGCBRCSSVOVNEIX-UHFFFAOYSA-N\u003c\/div\u003e\n                \u003c\/div\u003e\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eSMILES\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003eCOC1=C(C=CC(=C1C2=C(C=CC(=C2OC)Cl)P(C3=CC=CC=C3)C4=CC=CC=C4)P(C5=CC=CC=C5)C6=CC=CC=C6)Cl\u003c\/div\u003e\n                \u003c\/div\u003e\n            \n        \u003c\/div\u003e\n    \n\n    \u003c!-- Properties --\u003e\n    \n\n    \u003c!-- Safety Info --\u003e\n    \n\n    \u003c!-- Description --\u003e\n    \n    \u003ch2 class=\"section-header\"\u003eDescription\u003c\/h2\u003e\n    \u003cdiv class=\"html-area\"\u003e\n        Technical Notes:\u003cbr\u003e1. Ligand used in the ruthenium catalyzed, enantioselective hydrogenation of alkenes, carbonyls,\u003cbr\u003eand imines.\u003cbr\u003e2.Ligand used in the rhodium-catalyzed cyclization of acetylenic aldehydes .\u003cbr\u003e3. Ligand used in the iridium-c atalyzed hydrogenative coupling of alkynes to aromatic and aliphatic N-arylsulfonyl aldimines.\u003cbr\u003e4.Asymmetric Cu catalyzed propargylic substitution with amines,a and enamines.\u003cbr\u003e5.Catalytic desymmetrizing intramolecular Heck reaction.\u003cbr\u003e6.Assembly of 1,3-polyols.\u003cbr\u003e7.Pd-catalyzed diastereo\/enantios elective allylic alkylations of ketone enolates .\u003cbr\u003e8.Enantios elective vinylogous R eformatsky-type addition.\u003cbr\u003e9. Cu-catalyzed chemoselective preparation of 2-(pinacolato)boron- substituted allylcopper complexes\u003cbr\u003eand their In situ site-, diastereo-, and enantios elective additions to ketones .\n    \u003c\/div\u003e\n    \n\n    \u003c!-- Faq --\u003e\n    \n\n    \u003c!-- References --\u003e\n    \n    \u003ch2 class=\"section-header\"\u003e\n        \u003cspan style=\"display: block;\"\u003eReferences\u003c\/span\u003e\n        \u003cspan style=\"display: block; font-size: 1.2rem; color: #777; font-weight: lighter;\"\u003eData Source From Pubchem\u003c\/span\u003e\n    \u003c\/h2\u003e\n    \u003cdiv class=\"section-content\"\u003e\n        \n            \u003cdiv class=\"reference-item\"\u003e\n                \n                    \n                    \u003ca href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC11087250\" target=\"_blank\" rel=\"noopener noreferrer\"\u003e\n                        \u003ch3\u003eChelation enables selectivity control in enantioconvergent Suzuki–Miyaura cross-couplings on acyclic allylic systems\u003c\/h3\u003e\n                    \u003c\/a\u003e\n                    \n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Name: Nature Chemistry\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Date: 2024-02-08\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003eDOI: 10.1038\/s41557-023-01430-8\u003c\/div\u003e\n                \n            \u003c\/div\u003e\n        \n            \u003cdiv class=\"reference-item\"\u003e\n                \n                    \n                    \u003ca href=\"https:\/\/science-of-synthesis.thieme.com\/app\/text\/?id=SD-147-00217\" target=\"_blank\" rel=\"noopener noreferrer\"\u003e\n                        \u003ch3\u003eSynthesis from Diynes and Ethyl Glyoxalate\u003c\/h3\u003e\n                    \u003c\/a\u003e\n                    \n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Name: Science of Synthesis\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Date: 2023\u003c\/div\u003e\n                \n\n                \n            \u003c\/div\u003e\n        \n            \u003cdiv class=\"reference-item\"\u003e\n                \n                    \n                    \u003ca href=\"https:\/\/science-of-synthesis.thieme.com\/app\/text\/?id=SD-147-00216\" target=\"_blank\" rel=\"noopener noreferrer\"\u003e\n                        \u003ch3\u003eSynthesis from Diynes and α-Oxo Aldehydes\u003c\/h3\u003e\n                    \u003c\/a\u003e\n                    \n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Name: Science of Synthesis\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Date: 2023\u003c\/div\u003e\n                \n\n                \n            \u003c\/div\u003e\n        \n            \u003cdiv class=\"reference-item\"\u003e\n                \n                    \n                    \u003ca href=\"https:\/\/doi.org\/10.1055\/s-0042-1753070\" target=\"_blank\" rel=\"noopener noreferrer\"\u003e\n                        \u003ch3\u003eEnantioselective Synthesis of Tetrahydrofurans via a Palladium-Catalyzed [3+2] Cycloaddition\u003c\/h3\u003e\n                    \u003c\/a\u003e\n                    \n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Name: Synfacts\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Date: 2022-11-17\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003eDOI: 10.1055\/s-0042-1753070\u003c\/div\u003e\n                \n            \u003c\/div\u003e\n        \n            \u003cdiv class=\"reference-item\"\u003e\n                \n                    \n                    \u003ca href=\"https:\/\/doi.org\/10.1055\/s-0041-1737859\" target=\"_blank\" rel=\"noopener noreferrer\"\u003e\n                        \u003ch3\u003eAsymmetric Propargylic Substitution Enabled by Synergistic Nickel and Chiral Anion Catalysis\u003c\/h3\u003e\n                    \u003c\/a\u003e\n                    \n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Name: Synfacts\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Date: 2022-02-16\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003eDOI: 10.1055\/s-0041-1737859\u003c\/div\u003e\n                \n            \u003c\/div\u003e\n        \n    \u003c\/div\u003e\n    \n\n\n    \u003cscript\u003e\n        const coaSearchButton = document.getElementById('coa-search-button');\n        coaSearchButton.addEventListener('click', async function() {\n            const coaLinkInput = document.getElementById('coa-link-input');\n            const spinElement = document.querySelector('.search-spin');\n            const notFoundElement = document.querySelector('.coa-not-found');\n\n            const lot = coaLinkInput.value.trim().toUpperCase();\n            if (lot.length \u003e 0) {\n                spinElement.style.display = 'block';\n                notFoundElement.style.display = 'none';\n\n                const url = `https:\/\/web.jkchemical.com\/partial\/coaFileLotNumber\/${lot}`;\n                await fetch(url).then((res) =\u003e {\n                    if (res.status === 200) {\n                        window.open(url, '_blank');\n                    } else {\n                        notFoundElement.style.display = 'block';\n                    }\n                }).finally(() =\u003e {\n                    spinElement.style.display = 'none';\n                });\n            }\n        });\n    \u003c\/script\u003e\n\n\n\u003c\/div\u003e","brand":"US-Strem","offers":[{"title":"1×250mg","offer_id":45358225719486,"sku":"SC15-1056_250_MG","price":152.0,"currency_code":"USD","in_stock":true},{"title":"1×1g","offer_id":45358225752254,"sku":"SC15-1056_1_G","price":524.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0506\/0005\/0878\/files\/951147fd4c163619df3c8915e493b6ca.jpg?v=1788907669"},{"product_id":"q8815-0156","title":"(R)-(+)-2,2'-Bis(di-p-tolylphosphino)-6,6'-dimethoxy-1,1'-biphenyl, min. 97% | 133545-24-1","description":"\u003cstyle\u003e\n  \/* isQuote *\/\n  div.swatch.clearfix {\n    display:  unset ;\n  }\n\n  \/* Hide sku *\/\n  .product-sku, \n  #leadtimetext {\n    display: none !important;\n  }\n\n  \/* Square brackets *\/\n  span.l_bracket:before {\n    content: \"[\";\n  }\n  span.r_bracket:after {\n    content: \"]\";\n  }\n\n  \/* Hazard Symbols *\/\n  .ghs-symbols-row {\n    display: flex;\n    flex-wrap: wrap;\n    gap: 10px;\n  }\n\n  .hazard-symbol-container {\n    width: 50px;\n  }\n\n  .hazard-symbol {\n    object-fit: contain;\n    aspect-ratio: 1 \/ 1;\n    width: 100%;\n  }\n\n  \/* Section *\/\n  .section-header {\n    font-size: 2rem;\n    font-weight: bold;\n    color: #239ab7;\n    background-color: #f2f2f2;\n    padding: 10px;\n    border-radius: 4px;\n  }\n\n  .section-row {\n    display: grid;\n    grid-template-columns: repeat(8, 1fr);\n    padding: 6px 10px;\n    border-bottom: 1px solid #e0e0e0;\n  }\n\n  .section-content {\n    padding-bottom: 6px;\n  }\n\n  .section-content .section-row:last-child {\n    border-bottom: none;\n  }\n\n  .section-row .row-key {\n    grid-column: 1 \/ 3;\n    font-weight: bold;\n    align-self: center;\n  }\n\n  .section-row .row-value {\n    grid-column: 3 \/ 9;\n  }\n\n  .section-row ul li {\n    line-height: 2rem !important;\n    font-size: 1.3rem;\n  }\n\n  .html-area {\n    padding: 10px;\n    width: 100%;\n    overflow-x: auto;\n  }\n\n  .html-area {\n    padding: 10px;\n  }\n\n  .html-area p {\n    margin: 0 !important;\n  }\n\n  .hazard-grid {\n    display: grid;\n    grid-template-columns: repeat(6, 1fr);\n    gap: 0 10px;\n    font-size: 1.3rem;\n  }\n\n  .reference-item {\n    padding: 10px 10px;\n    border-bottom: 1px solid #e0e0e0;\n  }\n\n  .section-content .reference-item:last-child {\n    border-bottom: none;\n  }\n\n  .reference-item h3 {\n    font-size: 1.5rem !important;\n  }\n\n  .reference-item .publication-item {\n    font-size: 1.3rem !important;\n    line-height: 1.5rem !important;\n  }\n\n  \/* SDS Search *\/\n  .section-row .coa-search-container {\n    display: flex;\n    align-items: center;\n    margin-top: 6px;\n  }\n\n  .section-row .coa-search-container input {\n    border: 1px solid #e0e0e0;\n    height: 2.5rem;\n    border-top-left-radius: 0.5rem !important;\n    border-bottom-left-radius: 0.5rem !important;\n    padding: 3px 5px;\n  }\n\n  .section-row .coa-search-container button {\n    height: 2.5rem;\n    line-height: 2.5rem;\n    border-radius: 0 0.5rem 0.5rem 0;\n  }\n\n  .section-row .coa-search-container button .coa-search-button-content {\n    display: flex;\n    align-items: center;\n    justify-content: center;\n    gap: 3px;\n  }\n\n  .section-row .coa-search-container button .coa-search-button-content .search-spin {\n    display: none;\n    width: 2rem;\n  }\n\n  .section-row .coa-search-container .coa-not-found {\n    display: none;\n    margin: 0 0 0 2rem;\n    color: #ad2031;\n    font-size: 1.3rem;\n  }\n\n  \/* Table *\/\n  .html-area table {\n    width: 100%;\n    border-collapse: collapse;\n    margin: 15px 0;\n  }\n\n  .html-area table th,\n  .html-area table td {\n    border: 1px solid #e0e0e0;\n    padding: 5px 8px;\n  }\n\n  @media (max-width: 600px) {\n    .section-row {\n      grid-template-columns: repeat(1, 1fr);\n    }\n\n    .section-row .row-key {\n      grid-column: 1 \/ 2;\n    }\n\n    .section-row .row-value {\n      grid-column: 1 \/ 2;\n    }\n\n    .hazard-grid {\n      grid-template-columns: repeat(2, 1fr);\n      gap: 0 20px;\n    }\n  }\n  \n\u003c\/style\u003e\n\n\u003cdiv class=\"section\"\u003e\n  \n\n    \u003c!-- Order Info --\u003e\n    \u003ch2 class=\"section-header\"\u003eProduct Information\u003c\/h2\u003e\n    \u003cdiv class=\"section-content\"\u003e\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eProduct Name\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e(R)-(+)-2,2'-Bis(di-p-tolylphosphino)-6,6'-dimethoxy-1,1'-biphenyl, min. 97%\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n        \n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eBrand Name\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003eUS-Strem\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eProduct Number\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e15-0156\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eCAS\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e133545-24-1\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n\n        \n\n        \n\n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eCertificate of Analysis (COA)​\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e\n                \u003cdiv class=\"coa-search-container\"\u003e\n                    \u003cinput id=\"coa-link-input\" type=\"text\" placeholder=\"Enter Lot No.\"\u003e\n                    \u003cbutton id=\"coa-search-button\"\u003e\n                        \u003cdiv class=\"coa-search-button-content\"\u003e\n                            \u003csvg class=\"search-spin\" xmlns=\"http:\/\/www.w3.org\/2000\/svg\" viewbox=\"0 0 200 200\"\u003e\u003cradialgradient id=\"a7\" cx=\".66\" fx=\".66\" cy=\".3125\" fy=\".3125\" gradienttransform=\"scale(1.5)\"\u003e\u003cstop offset=\"0\" stop-color=\"#FFFFFF\"\u003e\u003c\/stop\u003e\u003cstop offset=\".3\" stop-color=\"#FFFFFF\" stop-opacity=\".9\"\u003e\u003c\/stop\u003e\u003cstop offset=\".6\" stop-color=\"#FFFFFF\" stop-opacity=\".6\"\u003e\u003c\/stop\u003e\u003cstop offset=\".8\" stop-color=\"#FFFFFF\" stop-opacity=\".3\"\u003e\u003c\/stop\u003e\u003cstop offset=\"1\" stop-color=\"#FFFFFF\" stop-opacity=\"0\"\u003e\u003c\/stop\u003e\u003c\/radialgradient\u003e\u003ccircle transform-origin=\"center\" fill=\"none\" stroke=\"url(#a7)\" stroke-width=\"15\" stroke-linecap=\"round\" stroke-dasharray=\"200 1000\" stroke-dashoffset=\"0\" cx=\"100\" cy=\"100\" r=\"70\"\u003e\u003canimatetransform type=\"rotate\" attributename=\"transform\" calcmode=\"spline\" dur=\"2\" values=\"360;0\" keytimes=\"0;1\" keysplines=\"0 0 1 1\" repeatcount=\"indefinite\"\u003e\u003c\/animatetransform\u003e\u003c\/circle\u003e\u003ccircle transform-origin=\"center\" fill=\"none\" opacity=\".2\" stroke=\"#FFFFFF\" stroke-width=\"15\" stroke-linecap=\"round\" cx=\"100\" cy=\"100\" r=\"70\"\u003e\u003c\/circle\u003e\u003c\/svg\u003e\n                            \u003cspan\u003eSearch\u003c\/span\u003e\n                        \u003c\/div\u003e\n                    \u003c\/button\u003e\n                    \u003cspan class=\"coa-not-found\"\u003eCOA not found\u003c\/span\u003e\n                \u003c\/div\u003e\n            \u003c\/div\u003e\n        \u003c\/div\u003e\n\n    \u003c\/div\u003e\n\n    \u003c!-- General Info --\u003e\n    \n        \u003ch2 class=\"section-header\"\u003eGeneral Information\u003c\/h2\u003e\n        \u003cdiv class=\"section-content\"\u003e\n            \n\n            \n            \u003cdiv class=\"section-row\"\u003e\n                \u003cdiv class=\"row-key\"\u003ePubChem CID\u003c\/div\u003e\n                \u003cdiv class=\"row-value\"\u003e22173705\u003c\/div\u003e\n            \u003c\/div\u003e\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eIUPAC Name\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003e\n\u003cspan class=\"l_bracket\"\u003e\u003c\/span\u003e2-\u003cspan class=\"l_bracket\"\u003e\u003c\/span\u003e2-bis(4-methylphenyl)phosphanyl-6-methoxyphenyl\u003cspan class=\"r_bracket\"\u003e\u003c\/span\u003e-3-methoxyphenyl\u003cspan class=\"r_bracket\"\u003e\u003c\/span\u003e-bis(4-methylphenyl)phosphane\u003c\/div\u003e\n                \u003c\/div\u003e\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eInChI Key\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003eDTMVLPFJTUJZAY-UHFFFAOYSA-N\u003c\/div\u003e\n                \u003c\/div\u003e\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eSMILES\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003eCC1=CC=C(C=C1)P(C2=CC=C(C=C2)C)C3=CC=CC(=C3C4=C(C=CC=C4P(C5=CC=C(C=C5)C)C6=CC=C(C=C6)C)OC)OC\u003c\/div\u003e\n                \u003c\/div\u003e\n            \n        \u003c\/div\u003e\n    \n\n    \u003c!-- Properties --\u003e\n    \n\n    \u003c!-- Safety Info --\u003e\n    \n\n    \u003c!-- Description --\u003e\n    \n    \u003ch2 class=\"section-header\"\u003eDescription\u003c\/h2\u003e\n    \u003cdiv class=\"html-area\"\u003e\n        Technical Notes:\u003cbr\u003eIn many respects the catalytic profile of the Me BIPHEP ligands is similar to that of other atropisomeric diphosphines such as binap and its many analogs. The nature of the PRz group strongly influences the catalytic performance of the metal complexes. The rhodium and ruthenium MeO-BIPHEP catalysts are highly effective for the hydrogenation of various c=o, C=c and C=N bonds and several synthetically useful C-c coupling reactions.\u003cbr\u003e1. See 15-0042\u003cbr\u003e2.Ru and Ir catalyzed dynamic kinetic resolution for the synthesis of hydroxy, amino acid derivatives.\u003cbr\u003e3. Ru-catalyzed asymmetric hydrogenation of ketones and alkenes.\u003cbr\u003e4. Ir catalyzed enantioselective hydrogenation of heteroaromatic compounds.\u003cbr\u003e5.Conjugate addition using 2-heteroaryl titanates and zinc reagents .\u003cbr\u003eReferences:\u003cbr\u003e1. Adv. Synth. C atal., 2004, 346, 842.\u003cbr\u003e2.Org. Lett., 2006, 8, 4573.\u003cbr\u003e3.Org. Process Res. Devel., 2001, 5, 438.\u003cbr\u003e4.J. Am. C hem. Soc., 2003, 125, 10536.\u003cbr\u003e5.Org. L ett., 2009, 1 1, 4200.\n    \u003c\/div\u003e\n    \n\n    \u003c!-- Faq --\u003e\n    \n\n    \u003c!-- References --\u003e\n    \n\n\n    \u003cscript\u003e\n        const coaSearchButton = document.getElementById('coa-search-button');\n        coaSearchButton.addEventListener('click', async function() {\n            const coaLinkInput = document.getElementById('coa-link-input');\n            const spinElement = document.querySelector('.search-spin');\n            const notFoundElement = document.querySelector('.coa-not-found');\n\n            const lot = coaLinkInput.value.trim().toUpperCase();\n            if (lot.length \u003e 0) {\n                spinElement.style.display = 'block';\n                notFoundElement.style.display = 'none';\n\n                const url = `https:\/\/web.jkchemical.com\/partial\/coaFileLotNumber\/${lot}`;\n                await fetch(url).then((res) =\u003e {\n                    if (res.status === 200) {\n                        window.open(url, 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\u003c\/script\u003e\n\n\n\u003c\/div\u003e","brand":"US-Strem","offers":[{"title":"1×100mg","offer_id":45358226178238,"sku":"SC15-0156_100_MG","price":99.0,"currency_code":"USD","in_stock":true},{"title":"1×10g","offer_id":45358226211006,"sku":"SC15-0156_10_G","price":4969.0,"currency_code":"USD","in_stock":true},{"title":"1×2g","offer_id":45358226243774,"sku":"SC15-0156_2_G","price":1244.0,"currency_code":"USD","in_stock":true},{"title":"1×500mg","offer_id":45358226276542,"sku":"SC15-0156_500_MG","price":366.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0506\/0005\/0878\/files\/a77139e0a9d055e9fc81371492ee834e.jpg?v=1788908278"},{"product_id":"q8815-0655","title":"(S)-(-)-2,2'-Bis(di-i-propylphosphino)-6,6'-dimethoxy-1,1'-biphenyl, min. 97% | 150971-43-0","description":"\u003cstyle\u003e\n  \/* isQuote *\/\n  div.swatch.clearfix {\n    display:  unset ;\n  }\n\n  \/* Hide sku *\/\n  .product-sku, \n  #leadtimetext {\n    display: none 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input {\n    border: 1px solid #e0e0e0;\n    height: 2.5rem;\n    border-top-left-radius: 0.5rem !important;\n    border-bottom-left-radius: 0.5rem !important;\n    padding: 3px 5px;\n  }\n\n  .section-row .coa-search-container button {\n    height: 2.5rem;\n    line-height: 2.5rem;\n    border-radius: 0 0.5rem 0.5rem 0;\n  }\n\n  .section-row .coa-search-container button .coa-search-button-content {\n    display: flex;\n    align-items: center;\n    justify-content: center;\n    gap: 3px;\n  }\n\n  .section-row .coa-search-container button .coa-search-button-content .search-spin {\n    display: none;\n    width: 2rem;\n  }\n\n  .section-row .coa-search-container .coa-not-found {\n    display: none;\n    margin: 0 0 0 2rem;\n    color: #ad2031;\n    font-size: 1.3rem;\n  }\n\n  \/* Table *\/\n  .html-area table {\n    width: 100%;\n    border-collapse: collapse;\n    margin: 15px 0;\n  }\n\n  .html-area table th,\n  .html-area table td {\n    border: 1px solid #e0e0e0;\n    padding: 5px 8px;\n  }\n\n  @media (max-width: 600px) {\n    .section-row {\n      grid-template-columns: repeat(1, 1fr);\n    }\n\n    .section-row .row-key {\n      grid-column: 1 \/ 2;\n    }\n\n    .section-row .row-value {\n      grid-column: 1 \/ 2;\n    }\n\n    .hazard-grid {\n      grid-template-columns: repeat(2, 1fr);\n      gap: 0 20px;\n    }\n  }\n  \n\u003c\/style\u003e\n\n\u003cdiv class=\"section\"\u003e\n  \n\n    \u003c!-- Order Info --\u003e\n    \u003ch2 class=\"section-header\"\u003eProduct Information\u003c\/h2\u003e\n    \u003cdiv class=\"section-content\"\u003e\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eProduct Name\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e(S)-(-)-2,2'-Bis(di-i-propylphosphino)-6,6'-dimethoxy-1,1'-biphenyl, min. 97%\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n        \n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eBrand Name\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003eUS-Strem\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eProduct Number\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e15-0655\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eCAS\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e150971-43-0\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n\n        \n\n        \n\n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eCertificate of Analysis (COA)​\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e\n                \u003cdiv class=\"coa-search-container\"\u003e\n                    \u003cinput id=\"coa-link-input\" type=\"text\" placeholder=\"Enter Lot No.\"\u003e\n                    \u003cbutton id=\"coa-search-button\"\u003e\n                        \u003cdiv class=\"coa-search-button-content\"\u003e\n                            \u003csvg class=\"search-spin\" xmlns=\"http:\/\/www.w3.org\/2000\/svg\" viewbox=\"0 0 200 200\"\u003e\u003cradialgradient id=\"a7\" cx=\".66\" fx=\".66\" cy=\".3125\" fy=\".3125\" gradienttransform=\"scale(1.5)\"\u003e\u003cstop offset=\"0\" stop-color=\"#FFFFFF\"\u003e\u003c\/stop\u003e\u003cstop offset=\".3\" stop-color=\"#FFFFFF\" stop-opacity=\".9\"\u003e\u003c\/stop\u003e\u003cstop offset=\".6\" stop-color=\"#FFFFFF\" stop-opacity=\".6\"\u003e\u003c\/stop\u003e\u003cstop offset=\".8\" stop-color=\"#FFFFFF\" stop-opacity=\".3\"\u003e\u003c\/stop\u003e\u003cstop offset=\"1\" stop-color=\"#FFFFFF\" stop-opacity=\"0\"\u003e\u003c\/stop\u003e\u003c\/radialgradient\u003e\u003ccircle transform-origin=\"center\" fill=\"none\" stroke=\"url(#a7)\" stroke-width=\"15\" stroke-linecap=\"round\" stroke-dasharray=\"200 1000\" stroke-dashoffset=\"0\" cx=\"100\" cy=\"100\" r=\"70\"\u003e\u003canimatetransform type=\"rotate\" attributename=\"transform\" calcmode=\"spline\" dur=\"2\" values=\"360;0\" keytimes=\"0;1\" keysplines=\"0 0 1 1\" repeatcount=\"indefinite\"\u003e\u003c\/animatetransform\u003e\u003c\/circle\u003e\u003ccircle transform-origin=\"center\" fill=\"none\" opacity=\".2\" stroke=\"#FFFFFF\" stroke-width=\"15\" stroke-linecap=\"round\" cx=\"100\" cy=\"100\" r=\"70\"\u003e\u003c\/circle\u003e\u003c\/svg\u003e\n                            \u003cspan\u003eSearch\u003c\/span\u003e\n                        \u003c\/div\u003e\n                    \u003c\/button\u003e\n                    \u003cspan class=\"coa-not-found\"\u003eCOA not found\u003c\/span\u003e\n                \u003c\/div\u003e\n            \u003c\/div\u003e\n        \u003c\/div\u003e\n\n    \u003c\/div\u003e\n\n    \u003c!-- General Info --\u003e\n    \n        \u003ch2 class=\"section-header\"\u003eGeneral Information\u003c\/h2\u003e\n        \u003cdiv class=\"section-content\"\u003e\n            \n\n            \n            \u003cdiv class=\"section-row\"\u003e\n                \u003cdiv class=\"row-key\"\u003ePubChem CID\u003c\/div\u003e\n                \u003cdiv class=\"row-value\"\u003e15823035\u003c\/div\u003e\n            \u003c\/div\u003e\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eIUPAC Name\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003e\n\u003cspan class=\"l_bracket\"\u003e\u003c\/span\u003e2-\u003cspan class=\"l_bracket\"\u003e\u003c\/span\u003e2-di(propan-2-yl)phosphanyl-6-methoxyphenyl\u003cspan class=\"r_bracket\"\u003e\u003c\/span\u003e-3-methoxyphenyl\u003cspan class=\"r_bracket\"\u003e\u003c\/span\u003e-di(propan-2-yl)phosphane\u003c\/div\u003e\n                \u003c\/div\u003e\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eInChI Key\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003eHLLUWVKDDQIKNF-UHFFFAOYSA-N\u003c\/div\u003e\n                \u003c\/div\u003e\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eSMILES\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003eCC(C)P(C1=CC=CC(=C1C2=C(C=CC=C2P(C(C)C)C(C)C)OC)OC)C(C)C\u003c\/div\u003e\n                \u003c\/div\u003e\n            \n        \u003c\/div\u003e\n    \n\n    \u003c!-- Properties --\u003e\n    \n\n    \u003c!-- Safety Info --\u003e\n    \n\n    \u003c!-- Description --\u003e\n    \n    \u003ch2 class=\"section-header\"\u003eDescription\u003c\/h2\u003e\n    \u003cdiv class=\"html-area\"\u003e\n        Technical Notes:\u003cbr\u003e1.Direct transformation of terminal alkynes to branched allylic sulfones.\u003cbr\u003e2.Novel palladium-catalyzed intramolecular addition of aryl bromides to aldehydes as a key to the synthesis of 3,3-dimethylchroman-4-ones and 3,3-dimethylchroman-4-ols.\u003cbr\u003e3.Ligand for Rh-Catalyzed Asymmetric Hydroalkynylation of Enamides.\u003cbr\u003eReferences:\u003cbr\u003e1. J. Am. Chem. Soc., 2014, 136, 16124. \r2. Chemistry Select, 2018, 3, 11333.\u003cbr\u003e3.J. Am. Chem. Soc.2018, 140, 506- -514.\n    \u003c\/div\u003e\n    \n\n    \u003c!-- Faq --\u003e\n    \n\n    \u003c!-- References --\u003e\n    \n    \u003ch2 class=\"section-header\"\u003e\n        \u003cspan style=\"display: block;\"\u003eReferences\u003c\/span\u003e\n        \u003cspan style=\"display: block; font-size: 1.2rem; color: #777; font-weight: lighter;\"\u003eData Source From Pubchem\u003c\/span\u003e\n    \u003c\/h2\u003e\n    \u003cdiv class=\"section-content\"\u003e\n        \n            \u003cdiv class=\"reference-item\"\u003e\n                \n                    \n                    \u003ca href=\"https:\/\/science-of-synthesis.thieme.com\/app\/text\/?id=SD-240-00112\" target=\"_blank\" rel=\"noopener noreferrer\"\u003e\n                        \u003ch3\u003eUsing Iridium Catalysis\u003c\/h3\u003e\n                    \u003c\/a\u003e\n                    \n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Name: Science of Synthesis\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Date: 2023\u003c\/div\u003e\n                \n\n                \n            \u003c\/div\u003e\n        \n            \u003cdiv class=\"reference-item\"\u003e\n                \n                    \n                    \u003ca href=\"https:\/\/doi.org\/10.1055\/s-0037-1610225\" target=\"_blank\" rel=\"noopener noreferrer\"\u003e\n                        \u003ch3\u003eCu-Catalyzed Conjugate Addition of Grignard Reagents to Thiochromones: An Enantioselective Pathway for Accessing 2-Alkylthiochromanones\u003c\/h3\u003e\n                    \u003c\/a\u003e\n                    \n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Name: Synlett\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Date: 2018-08-02\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003eDOI: 10.1055\/s-0037-1610225\u003c\/div\u003e\n                \n            \u003c\/div\u003e\n        \n            \u003cdiv class=\"reference-item\"\u003e\n                \n                    \n                    \u003ca href=\"https:\/\/doi.org\/10.1055\/s-0030-1260804\" target=\"_blank\" rel=\"noopener noreferrer\"\u003e\n                        \u003ch3\u003ePhosphine-Catalyzed [3+2] Annulation of Cyanoallenes\u003c\/h3\u003e\n                    \u003c\/a\u003e\n                    \n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Name: Synlett\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Date: 2011-06-21\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003eDOI: 10.1055\/s-0030-1260804\u003c\/div\u003e\n                \n            \u003c\/div\u003e\n        \n    \u003c\/div\u003e\n    \n\n\n    \u003cscript\u003e\n        const coaSearchButton = document.getElementById('coa-search-button');\n        coaSearchButton.addEventListener('click', async function() {\n            const coaLinkInput = document.getElementById('coa-link-input');\n            const spinElement = document.querySelector('.search-spin');\n            const notFoundElement = document.querySelector('.coa-not-found');\n\n            const lot = coaLinkInput.value.trim().toUpperCase();\n            if (lot.length \u003e 0) {\n                spinElement.style.display = 'block';\n                notFoundElement.style.display = 'none';\n\n                const url = `https:\/\/web.jkchemical.com\/partial\/coaFileLotNumber\/${lot}`;\n                await fetch(url).then((res) =\u003e {\n                    if (res.status === 200) {\n         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\u003c\/script\u003e\n\n\n\u003c\/div\u003e","brand":"US-Strem","offers":[{"title":"1×10g","offer_id":45358226702526,"sku":"SC15-0655_10_G","price":4969.0,"currency_code":"USD","in_stock":true},{"title":"1×100mg","offer_id":45358226735294,"sku":"SC15-0655_100_MG","price":99.0,"currency_code":"USD","in_stock":true},{"title":"1×500mg","offer_id":45358226768062,"sku":"SC15-0655_500_MG","price":366.0,"currency_code":"USD","in_stock":true},{"title":"1×2g","offer_id":45358226800830,"sku":"SC15-0655_2_G","price":1244.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0506\/0005\/0878\/files\/0c2eb0bbd468534b621e737046c1280c.jpg?v=1788907810"},{"product_id":"q8815-0145","title":"2,2'-Bis(diphenylphosphino)-1,1'-biphenyl, 98% BIPHEP | 84783-64-2","description":"\u003cstyle\u003e\n  \/* isQuote *\/\n  div.swatch.clearfix {\n    display:  unset ;\n  }\n\n  \/* Hide sku *\/\n  .product-sku, \n  #leadtimetext {\n    display: none !important;\n  }\n\n  \/* 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@media (max-width: 600px) {\n    .section-row {\n      grid-template-columns: repeat(1, 1fr);\n    }\n\n    .section-row .row-key {\n      grid-column: 1 \/ 2;\n    }\n\n    .section-row .row-value {\n      grid-column: 1 \/ 2;\n    }\n\n    .hazard-grid {\n      grid-template-columns: repeat(2, 1fr);\n      gap: 0 20px;\n    }\n  }\n  \n\u003c\/style\u003e\n\n\u003cdiv class=\"section\"\u003e\n  \n\n    \u003c!-- Order Info --\u003e\n    \u003ch2 class=\"section-header\"\u003eProduct Information\u003c\/h2\u003e\n    \u003cdiv class=\"section-content\"\u003e\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eProduct Name\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e2,2'-Bis(diphenylphosphino)-1,1'-biphenyl, 98% BIPHEP\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n        \n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eBrand Name\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003eUS-Strem\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eProduct Number\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e15-0145\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eCAS\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e84783-64-2\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n\n        \n\n        \n\n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eCertificate of Analysis (COA)​\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e\n                \u003cdiv class=\"coa-search-container\"\u003e\n                    \u003cinput id=\"coa-link-input\" type=\"text\" placeholder=\"Enter Lot No.\"\u003e\n            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stroke-dashoffset=\"0\" cx=\"100\" cy=\"100\" r=\"70\"\u003e\u003canimatetransform type=\"rotate\" attributename=\"transform\" calcmode=\"spline\" dur=\"2\" values=\"360;0\" keytimes=\"0;1\" keysplines=\"0 0 1 1\" repeatcount=\"indefinite\"\u003e\u003c\/animatetransform\u003e\u003c\/circle\u003e\u003ccircle transform-origin=\"center\" fill=\"none\" opacity=\".2\" stroke=\"#FFFFFF\" stroke-width=\"15\" stroke-linecap=\"round\" cx=\"100\" cy=\"100\" r=\"70\"\u003e\u003c\/circle\u003e\u003c\/svg\u003e\n                            \u003cspan\u003eSearch\u003c\/span\u003e\n                        \u003c\/div\u003e\n                    \u003c\/button\u003e\n                    \u003cspan class=\"coa-not-found\"\u003eCOA not found\u003c\/span\u003e\n                \u003c\/div\u003e\n            \u003c\/div\u003e\n        \u003c\/div\u003e\n\n    \u003c\/div\u003e\n\n    \u003c!-- General Info --\u003e\n    \n        \u003ch2 class=\"section-header\"\u003eGeneral Information\u003c\/h2\u003e\n        \u003cdiv class=\"section-content\"\u003e\n            \n\n            \n            \u003cdiv class=\"section-row\"\u003e\n                \u003cdiv class=\"row-key\"\u003ePubChem CID\u003c\/div\u003e\n                \u003cdiv class=\"row-value\"\u003e2734940\u003c\/div\u003e\n            \u003c\/div\u003e\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eIUPAC Name\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003e\n\u003cspan class=\"l_bracket\"\u003e\u003c\/span\u003e2-(2-diphenylphosphanylphenyl)phenyl\u003cspan class=\"r_bracket\"\u003e\u003c\/span\u003e-diphenylphosphane\u003c\/div\u003e\n                \u003c\/div\u003e\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eInChI Key\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003eGRTJBNJOHNTQBO-UHFFFAOYSA-N\u003c\/div\u003e\n                \u003c\/div\u003e\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eSMILES\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003eC1=CC=C(C=C1)P(C2=CC=CC=C2)C3=CC=CC=C3C4=CC=CC=C4P(C5=CC=CC=C5)C6=CC=CC=C6\u003c\/div\u003e\n                \u003c\/div\u003e\n            \n        \u003c\/div\u003e\n    \n\n    \u003c!-- Properties --\u003e\n    \n\n    \u003c!-- Safety Info --\u003e\n    \n\n    \u003c!-- Description --\u003e\n    \n    \u003ch2 class=\"section-header\"\u003eDescription\u003c\/h2\u003e\n    \u003cdiv class=\"html-area\"\u003e\n        Technical Notes:\u003cbr\u003e1. Supporting ligand in a chiral diamine ruthenium system for the enantiosele ctive hyd rogenation of ketones.\u003cbr\u003e2. Useful ligand for palladium-catalyzed amination and Kumada cross coupling reactions\u003cbr\u003e3.Useful ligand for palladium-catalyzed synthesis of butatrenes.\u003cbr\u003e4.Useful ligand for iridium-catalyzed c-c cross-coupling of allenes with primary alcohols via transfer hydrogenation\u003cbr\u003e5.Useful ligand for iridium-catalyzed C-C cross-coupling of dienes with primary alcohols via transfer hyd rogenation.\u003cbr\u003e6.Useful ligand for iridium- catalyzed C-C cross coupling of allylic gem dicarboxylates with aldehydes via transfer hydrogenation. Useful ligand for the palladium catalyzed synthesis of chiral allenylsilanes.\u003cbr\u003e7.Ruthenium- catalyzed synthesis of indoles\u003cbr\u003e8.Ruthenium-catalyzed oxidative cyclization .\u003cbr\u003e9Rhodium catalyzed boron arylation.\n    \u003c\/div\u003e\n    \n\n    \u003c!-- Faq --\u003e\n    \n\n    \u003c!-- References --\u003e\n    \n    \u003ch2 class=\"section-header\"\u003e\n        \u003cspan style=\"display: block;\"\u003eReferences\u003c\/span\u003e\n        \u003cspan style=\"display: block; font-size: 1.2rem; color: #777; font-weight: lighter;\"\u003eData Source From Pubchem\u003c\/span\u003e\n    \u003c\/h2\u003e\n    \u003cdiv class=\"section-content\"\u003e\n        \n            \u003cdiv class=\"reference-item\"\u003e\n                \n                    \n                    \u003ca href=\"https:\/\/science-of-synthesis.thieme.com\/app\/text\/?id=SD-120-00286\" target=\"_blank\" rel=\"noopener noreferrer\"\u003e\n                        \u003ch3\u003eIridium-Catalyzed “Reverse” Prenylation of Carboxylic Acids\u003c\/h3\u003e\n                    \u003c\/a\u003e\n                    \n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Name: Science of Synthesis\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Date: 2024\u003c\/div\u003e\n                \n\n                \n            \u003c\/div\u003e\n        \n            \u003cdiv class=\"reference-item\"\u003e\n                \n                    \n                    \u003ca href=\"https:\/\/science-of-synthesis.thieme.com\/app\/text\/?id=SD-147-00193\" target=\"_blank\" rel=\"noopener noreferrer\"\u003e\n                        \u003ch3\u003eUsing Copper Catalysts\u003c\/h3\u003e\n                    \u003c\/a\u003e\n                    \n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Name: Science of Synthesis\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Date: 2023\u003c\/div\u003e\n                \n\n                \n            \u003c\/div\u003e\n        \n            \u003cdiv class=\"reference-item\"\u003e\n                \n                    \n                    \u003ca href=\"https:\/\/science-of-synthesis.thieme.com\/app\/text\/?id=SD-147-00218\" target=\"_blank\" rel=\"noopener noreferrer\"\u003e\n                        \u003ch3\u003eSynthesis from Enynes and α-Oxo Aldehydes\u003c\/h3\u003e\n                    \u003c\/a\u003e\n                    \n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Name: Science of Synthesis\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Date: 2023\u003c\/div\u003e\n                \n\n                \n            \u003c\/div\u003e\n        \n            \u003cdiv class=\"reference-item\"\u003e\n                \n                    \n                    \u003ca href=\"https:\/\/doi.org\/10.1055\/s-0041-1738059\" target=\"_blank\" rel=\"noopener noreferrer\"\u003e\n                        \u003ch3\u003eSynthesis of Armchair- and Chiral-Type Belts\u003c\/h3\u003e\n                    \u003c\/a\u003e\n                    \n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Name: Synfacts\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Date: 2022-04-20\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003eDOI: 10.1055\/s-0041-1738059\u003c\/div\u003e\n                \n            \u003c\/div\u003e\n        \n            \u003cdiv class=\"reference-item\"\u003e\n                \n                    \n                    \u003ca href=\"https:\/\/doi.org\/10.1038\/s44160-022-00043-2\" target=\"_blank\" rel=\"noopener noreferrer\"\u003e\n                        \u003ch3\u003eStereoselective cyclohexadienylamine synthesis through rhodium-catalysed [2+2+2] cyclotrimerization\u003c\/h3\u003e\n                    \u003c\/a\u003e\n                    \n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Name: Nature Synthesis\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Date: 2022-03-28\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003eDOI: 10.1038\/s44160-022-00043-2\u003c\/div\u003e\n                \n            \u003c\/div\u003e\n        \n    \u003c\/div\u003e\n    \n\n\n    \u003cscript\u003e\n        const 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stop-opacity=\"0\"\u003e\u003c\/stop\u003e\u003c\/radialgradient\u003e\u003ccircle transform-origin=\"center\" fill=\"none\" stroke=\"url(#a7)\" stroke-width=\"15\" stroke-linecap=\"round\" stroke-dasharray=\"200 1000\" stroke-dashoffset=\"0\" cx=\"100\" cy=\"100\" r=\"70\"\u003e\u003canimatetransform type=\"rotate\" attributename=\"transform\" calcmode=\"spline\" dur=\"2\" values=\"360;0\" keytimes=\"0;1\" keysplines=\"0 0 1 1\" repeatcount=\"indefinite\"\u003e\u003c\/animatetransform\u003e\u003c\/circle\u003e\u003ccircle transform-origin=\"center\" fill=\"none\" opacity=\".2\" stroke=\"#FFFFFF\" stroke-width=\"15\" stroke-linecap=\"round\" cx=\"100\" cy=\"100\" r=\"70\"\u003e\u003c\/circle\u003e\u003c\/svg\u003e\n                            \u003cspan\u003eSearch\u003c\/span\u003e\n                        \u003c\/div\u003e\n                    \u003c\/button\u003e\n                    \u003cspan class=\"coa-not-found\"\u003eCOA not found\u003c\/span\u003e\n                \u003c\/div\u003e\n            \u003c\/div\u003e\n        \u003c\/div\u003e\n\n    \u003c\/div\u003e\n\n    \u003c!-- General Info --\u003e\n    \n        \u003ch2 class=\"section-header\"\u003eGeneral Information\u003c\/h2\u003e\n        \u003cdiv class=\"section-content\"\u003e\n            \n\n            \n            \u003cdiv class=\"section-row\"\u003e\n                \u003cdiv class=\"row-key\"\u003ePubChem CID\u003c\/div\u003e\n                \u003cdiv class=\"row-value\"\u003e11227787\u003c\/div\u003e\n            \u003c\/div\u003e\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eIUPAC Name\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003e\n\u003cspan class=\"l_bracket\"\u003e\u003c\/span\u003e2-\u003cspan class=\"l_bracket\"\u003e\u003c\/span\u003e2-bis(3,5-dimethylphenyl)phosphanyl-6-methoxyphenyl\u003cspan class=\"r_bracket\"\u003e\u003c\/span\u003e-3-methoxyphenyl\u003cspan class=\"r_bracket\"\u003e\u003c\/span\u003e-bis(3,5-dimethylphenyl)phosphane\u003c\/div\u003e\n                \u003c\/div\u003e\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eInChI Key\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003eIMUHNRWTDUVXOU-UHFFFAOYSA-N\u003c\/div\u003e\n                \u003c\/div\u003e\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eSMILES\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003eCC1=CC(=CC(=C1)P(C2=CC=CC(=C2C3=C(C=CC=C3P(C4=CC(=CC(=C4)C)C)C5=CC(=CC(=C5)C)C)OC)OC)C6=CC(=CC(=C6)C)C)C\u003c\/div\u003e\n                \u003c\/div\u003e\n            \n        \u003c\/div\u003e\n    \n\n    \u003c!-- Properties --\u003e\n    \n\n    \u003c!-- Safety Info --\u003e\n    \n        \u003ch2 class=\"section-header\"\u003eSafety Information\u003c\/h2\u003e\n        \u003cdiv class=\"section-content\"\u003e\n            \n\n            \n\n            \n\n            \n\n            \n\n            \n\n            \n\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eStorage Condition\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003e\n                        Store at 2-8℃\n                    \u003c\/div\u003e\n                \u003c\/div\u003e\n            \n        \u003c\/div\u003e\n    \n\n    \u003c!-- Description --\u003e\n    \n    \u003ch2 class=\"section-header\"\u003eDescription\u003c\/h2\u003e\n    \u003cdiv class=\"html-area\"\u003e\n        Technical Note：\r1.See 15-0042.\u003cbr\u003e2.Ru and Ir catalyzed dynamic kinetic resolution for the synthesis of hydroxy, amino acidderivatives.\u003cbr\u003e3.Ru-catalyzed asymmetric hydrogenation of ketones and alkenes.\u003cbr\u003e4.Enantioselective copper-catalyzed asymmetric hydrosilylation of aryl ketones\u003cbr\u003e5.Synthesis of chiral 3-substituted indanones via an enantioselective reductive-Heck reaction. \r6.Gold(l)-catalyzed enantioselective ring expansion of allenylcyclo propanols.\u003cbr\u003e7. Conjugate addition using 2-heteroaryl titanates and zinc reagents.\u003cbr\u003eReferences:\u003cbr\u003e1.Adv. Synth. Catal., 2004, 346, 842.\u003cbr\u003e2.Org. Lett, 2006, 8, 4573.\u003cbr\u003e3.Org. Process Res. Devel., 2001, 5, 438.\u003cbr\u003e4.J. Am. Chem. Soc., 2001, 123, 1291 5.J. Org. Chem., 2007, 72, 9253.\u003cbr\u003e6.J. Am. Chem. Soc., 2009, 131, 91 78. 7.Org. Lett., 2009, 11, 4200.\n    \u003c\/div\u003e\n    \n\n    \u003c!-- Faq --\u003e\n    \n\n    \u003c!-- References --\u003e\n    \n    \u003ch2 class=\"section-header\"\u003e\n        \u003cspan style=\"display: block;\"\u003eReferences\u003c\/span\u003e\n        \u003cspan style=\"display: block; font-size: 1.2rem; color: #777; font-weight: lighter;\"\u003eData Source From Pubchem\u003c\/span\u003e\n    \u003c\/h2\u003e\n    \u003cdiv class=\"section-content\"\u003e\n        \n            \u003cdiv class=\"reference-item\"\u003e\n                \n                    \n                    \u003ca href=\"https:\/\/doi.org\/10.1055\/s-0036-1588709\" target=\"_blank\" rel=\"noopener noreferrer\"\u003e\n                        \u003ch3\u003eIon-Pair-Directed meta-Selective C–H Borylation of Aromatic Quaternary Ammonium Salts\u003c\/h3\u003e\n                    \u003c\/a\u003e\n                    \n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Name: Synlett\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Date: 2017-02-13\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003eDOI: 10.1055\/s-0036-1588709\u003c\/div\u003e\n                \n            \u003c\/div\u003e\n        \n            \u003cdiv class=\"reference-item\"\u003e\n                \n                    \n                    \u003ca href=\"https:\/\/science-of-synthesis.thieme.com\/app\/text\/?id=SD-221-00044\" target=\"_blank\" rel=\"noopener noreferrer\"\u003e\n                        \u003ch3\u003eReactions from Aryl Halides and Pseudohalides\u003c\/h3\u003e\n                    \u003c\/a\u003e\n                    \n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Name: Science of Synthesis\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Date: 2016\u003c\/div\u003e\n                \n\n                \n            \u003c\/div\u003e\n        \n            \u003cdiv class=\"reference-item\"\u003e\n                \n                    \n                    \u003ca href=\"https:\/\/science-of-synthesis.thieme.com\/app\/text\/?id=SD-106-00204\" target=\"_blank\" rel=\"noopener noreferrer\"\u003e\n                        \u003ch3\u003eUse in Alkene and Alkyne Hydroborations\u003c\/h3\u003e\n                    \u003c\/a\u003e\n                    \n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Name: Science of Synthesis\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Date: 2014\u003c\/div\u003e\n                \n\n                \n            \u003c\/div\u003e\n        \n            \u003cdiv class=\"reference-item\"\u003e\n                \n                    \n                    \u003ca href=\"https:\/\/doi.org\/10.1007\/978-3-642-19472-6_2\" target=\"_blank\" rel=\"noopener noreferrer\"\u003e\n                        \u003ch3\u003eChiral Phosphorus Ligands with Interesting Properties and Practical Applications\u003c\/h3\u003e\n                    \u003c\/a\u003e\n                    \n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Name: Asymmetric Catalysis from a Chinese Perspective\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Date: 2011-05-31\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003eDOI: 10.1007\/978-3-642-19472-6_2\u003c\/div\u003e\n                \n            \u003c\/div\u003e\n        \n            \u003cdiv class=\"reference-item\"\u003e\n                \n                    \n                    \u003ca href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/20112312\" target=\"_blank\" rel=\"noopener noreferrer\"\u003e\n                        \u003ch3\u003eChiral and Nonchiral [OsX2(diphosphane)(diamine)] (X: Cl, OCH2CF3) Complexes for Fast Hydrogenation of Carbonyl Compounds\u003c\/h3\u003e\n                    \u003c\/a\u003e\n                    \n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Name: Chemistry (Weinheim an der Bergstrasse, Germany)\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Date: 2010-03-08\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003eDOI: 10.1002\/chem.200902809\u003c\/div\u003e\n                \n            \u003c\/div\u003e\n        \n    \u003c\/div\u003e\n    \n\n\n    \u003cscript\u003e\n        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border-collapse: collapse;\n    margin: 15px 0;\n  }\n\n  .html-area table th,\n  .html-area table td {\n    border: 1px solid #e0e0e0;\n    padding: 5px 8px;\n  }\n\n  @media (max-width: 600px) {\n    .section-row {\n      grid-template-columns: repeat(1, 1fr);\n    }\n\n    .section-row .row-key {\n      grid-column: 1 \/ 2;\n    }\n\n    .section-row .row-value {\n      grid-column: 1 \/ 2;\n    }\n\n    .hazard-grid {\n      grid-template-columns: repeat(2, 1fr);\n      gap: 0 20px;\n    }\n  }\n  \n\u003c\/style\u003e\n\n\u003cdiv class=\"section\"\u003e\n  \n\n    \u003c!-- Order Info --\u003e\n    \u003ch2 class=\"section-header\"\u003eProduct Information\u003c\/h2\u003e\n    \u003cdiv class=\"section-content\"\u003e\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eProduct Name\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e(R)-(+)-2,2'-Bis\u003cspan class=\"l_bracket\"\u003e\u003c\/span\u003edi(3,5-xylyl)phosphino\u003cspan class=\"r_bracket\"\u003e\u003c\/span\u003e-6,6'-dimethoxy-1,1'-biphenyl, min. 97%\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n        \n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eBrand Name\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003eUS-Strem\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eProduct Number\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e15-0488\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eCAS\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e394248-45-4\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n\n        \n\n        \n\n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eCertificate of Analysis (COA)​\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e\n                \u003cdiv class=\"coa-search-container\"\u003e\n                    \u003cinput id=\"coa-link-input\" type=\"text\" placeholder=\"Enter Lot No.\"\u003e\n                    \u003cbutton id=\"coa-search-button\"\u003e\n                        \u003cdiv class=\"coa-search-button-content\"\u003e\n                            \u003csvg class=\"search-spin\" xmlns=\"http:\/\/www.w3.org\/2000\/svg\" viewbox=\"0 0 200 200\"\u003e\u003cradialgradient id=\"a7\" cx=\".66\" fx=\".66\" cy=\".3125\" fy=\".3125\" gradienttransform=\"scale(1.5)\"\u003e\u003cstop offset=\"0\" stop-color=\"#FFFFFF\"\u003e\u003c\/stop\u003e\u003cstop offset=\".3\" stop-color=\"#FFFFFF\" stop-opacity=\".9\"\u003e\u003c\/stop\u003e\u003cstop offset=\".6\" stop-color=\"#FFFFFF\" stop-opacity=\".6\"\u003e\u003c\/stop\u003e\u003cstop offset=\".8\" stop-color=\"#FFFFFF\" stop-opacity=\".3\"\u003e\u003c\/stop\u003e\u003cstop offset=\"1\" stop-color=\"#FFFFFF\" stop-opacity=\"0\"\u003e\u003c\/stop\u003e\u003c\/radialgradient\u003e\u003ccircle transform-origin=\"center\" fill=\"none\" stroke=\"url(#a7)\" stroke-width=\"15\" stroke-linecap=\"round\" stroke-dasharray=\"200 1000\" stroke-dashoffset=\"0\" cx=\"100\" cy=\"100\" r=\"70\"\u003e\u003canimatetransform type=\"rotate\" attributename=\"transform\" calcmode=\"spline\" dur=\"2\" values=\"360;0\" keytimes=\"0;1\" keysplines=\"0 0 1 1\" repeatcount=\"indefinite\"\u003e\u003c\/animatetransform\u003e\u003c\/circle\u003e\u003ccircle transform-origin=\"center\" fill=\"none\" opacity=\".2\" stroke=\"#FFFFFF\" stroke-width=\"15\" stroke-linecap=\"round\" cx=\"100\" cy=\"100\" r=\"70\"\u003e\u003c\/circle\u003e\u003c\/svg\u003e\n                            \u003cspan\u003eSearch\u003c\/span\u003e\n                        \u003c\/div\u003e\n                    \u003c\/button\u003e\n                    \u003cspan class=\"coa-not-found\"\u003eCOA not found\u003c\/span\u003e\n                \u003c\/div\u003e\n            \u003c\/div\u003e\n        \u003c\/div\u003e\n\n    \u003c\/div\u003e\n\n    \u003c!-- General Info --\u003e\n    \n        \u003ch2 class=\"section-header\"\u003eGeneral Information\u003c\/h2\u003e\n        \u003cdiv class=\"section-content\"\u003e\n            \n\n            \n            \u003cdiv class=\"section-row\"\u003e\n                \u003cdiv class=\"row-key\"\u003ePubChem CID\u003c\/div\u003e\n                \u003cdiv class=\"row-value\"\u003e11227787\u003c\/div\u003e\n            \u003c\/div\u003e\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eIUPAC Name\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003e\n\u003cspan class=\"l_bracket\"\u003e\u003c\/span\u003e2-\u003cspan class=\"l_bracket\"\u003e\u003c\/span\u003e2-bis(3,5-dimethylphenyl)phosphanyl-6-methoxyphenyl\u003cspan class=\"r_bracket\"\u003e\u003c\/span\u003e-3-methoxyphenyl\u003cspan class=\"r_bracket\"\u003e\u003c\/span\u003e-bis(3,5-dimethylphenyl)phosphane\u003c\/div\u003e\n                \u003c\/div\u003e\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eInChI Key\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003eIMUHNRWTDUVXOU-UHFFFAOYSA-N\u003c\/div\u003e\n                \u003c\/div\u003e\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eSMILES\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003eCC1=CC(=CC(=C1)P(C2=CC=CC(=C2C3=C(C=CC=C3P(C4=CC(=CC(=C4)C)C)C5=CC(=CC(=C5)C)C)OC)OC)C6=CC(=CC(=C6)C)C)C\u003c\/div\u003e\n                \u003c\/div\u003e\n            \n        \u003c\/div\u003e\n    \n\n    \u003c!-- Properties --\u003e\n    \n\n    \u003c!-- Safety Info --\u003e\n    \n        \u003ch2 class=\"section-header\"\u003eSafety Information\u003c\/h2\u003e\n        \u003cdiv class=\"section-content\"\u003e\n            \n\n            \n\n            \n\n            \n\n            \n\n            \n\n            \n\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eStorage Condition\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003e\n                        Store at 2-8℃\n                    \u003c\/div\u003e\n                \u003c\/div\u003e\n            \n        \u003c\/div\u003e\n    \n\n    \u003c!-- Description --\u003e\n    \n    \u003ch2 class=\"section-header\"\u003eDescription\u003c\/h2\u003e\n    \u003cdiv class=\"html-area\"\u003e\n        Technical Note\r1.See 15-0042.\u003cbr\u003e2.Ru and Ir catalyzed dynamic kinetic resolution for the synthesis of hydroxy, amino acid derivatives\u003cbr\u003e3.Ru- catalyzed asymmetric hydrogenation of ketones and alkenes.\u003cbr\u003e4.Enantioselective copper-catalyzed asymmetric hydrosilylation of aryl ketones.\u003cbr\u003e5.Synthesis of chiral 3-substituted indanones via an enantioselective reductive-Heck reaction.\u003cbr\u003e6.Gold(1)- catalyzed enantioselective ring expansion of allenylcyclopropanols.\u003cbr\u003e7.Conjugate addition using 2-heteroaryl titanates and zinc reagents .\u003cbr\u003eReferences:\u003cbr\u003e1. Adv. Synth. Catal., 2004, 346, 842.\u003cbr\u003e2.Org. L ett., 2006, 8, 4573.\u003cbr\u003e3.Org. Process Res. Devel., 2001, 5, 438.\u003cbr\u003e4.J. Am. Chem. Soc., 2001, 123, 1291 \u003cbr\u003e7.\r5.J. Org. Chem., 2007, 72, 9253.\u003cbr\u003e6.J. Am. Chem. Soc., 2009, 131, 91 78.\u003cbr\u003e7.Org. L ett., 2009, 11, 4200.\n    \u003c\/div\u003e\n    \n\n    \u003c!-- Faq --\u003e\n    \n\n    \u003c!-- References --\u003e\n    \n    \u003ch2 class=\"section-header\"\u003e\n        \u003cspan style=\"display: block;\"\u003eReferences\u003c\/span\u003e\n        \u003cspan style=\"display: block; font-size: 1.2rem; color: #777; font-weight: lighter;\"\u003eData Source From Pubchem\u003c\/span\u003e\n    \u003c\/h2\u003e\n    \u003cdiv class=\"section-content\"\u003e\n        \n            \u003cdiv class=\"reference-item\"\u003e\n                \n                    \n                    \u003ca href=\"https:\/\/doi.org\/10.1055\/s-0036-1588709\" target=\"_blank\" rel=\"noopener noreferrer\"\u003e\n                        \u003ch3\u003eIon-Pair-Directed meta-Selective C–H Borylation of Aromatic Quaternary Ammonium Salts\u003c\/h3\u003e\n                    \u003c\/a\u003e\n                    \n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Name: Synlett\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Date: 2017-02-13\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003eDOI: 10.1055\/s-0036-1588709\u003c\/div\u003e\n                \n            \u003c\/div\u003e\n        \n            \u003cdiv class=\"reference-item\"\u003e\n                \n                    \n                    \u003ca href=\"https:\/\/science-of-synthesis.thieme.com\/app\/text\/?id=SD-221-00044\" target=\"_blank\" rel=\"noopener noreferrer\"\u003e\n                        \u003ch3\u003eReactions from Aryl Halides and Pseudohalides\u003c\/h3\u003e\n                    \u003c\/a\u003e\n                    \n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Name: Science of Synthesis\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Date: 2016\u003c\/div\u003e\n                \n\n                \n            \u003c\/div\u003e\n        \n            \u003cdiv class=\"reference-item\"\u003e\n                \n                    \n                    \u003ca href=\"https:\/\/science-of-synthesis.thieme.com\/app\/text\/?id=SD-106-00204\" target=\"_blank\" rel=\"noopener noreferrer\"\u003e\n                        \u003ch3\u003eUse in Alkene and Alkyne Hydroborations\u003c\/h3\u003e\n                    \u003c\/a\u003e\n                    \n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Name: Science of Synthesis\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Date: 2014\u003c\/div\u003e\n                \n\n                \n            \u003c\/div\u003e\n        \n            \u003cdiv class=\"reference-item\"\u003e\n                \n                    \n                    \u003ca href=\"https:\/\/doi.org\/10.1007\/978-3-642-19472-6_2\" target=\"_blank\" rel=\"noopener noreferrer\"\u003e\n                        \u003ch3\u003eChiral Phosphorus Ligands with Interesting Properties and Practical Applications\u003c\/h3\u003e\n                    \u003c\/a\u003e\n                    \n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Name: Asymmetric Catalysis from a Chinese Perspective\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Date: 2011-05-31\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003eDOI: 10.1007\/978-3-642-19472-6_2\u003c\/div\u003e\n                \n            \u003c\/div\u003e\n        \n            \u003cdiv class=\"reference-item\"\u003e\n                \n                    \n                    \u003ca href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/20112312\" target=\"_blank\" rel=\"noopener noreferrer\"\u003e\n                        \u003ch3\u003eChiral and Nonchiral [OsX2(diphosphane)(diamine)] (X: Cl, OCH2CF3) Complexes for Fast Hydrogenation of Carbonyl Compounds\u003c\/h3\u003e\n                    \u003c\/a\u003e\n                    \n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Name: Chemistry (Weinheim an der Bergstrasse, Germany)\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Date: 2010-03-08\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003eDOI: 10.1002\/chem.200902809\u003c\/div\u003e\n                \n            \u003c\/div\u003e\n        \n    \u003c\/div\u003e\n    \n\n\n    \u003cscript\u003e\n        const coaSearchButton = document.getElementById('coa-search-button');\n        coaSearchButton.addEventListener('click', async function() {\n            const coaLinkInput = document.getElementById('coa-link-input');\n            const spinElement = document.querySelector('.search-spin');\n            const notFoundElement = document.querySelector('.coa-not-found');\n\n            const lot = coaLinkInput.value.trim().toUpperCase();\n            if (lot.length \u003e 0) {\n                spinElement.style.display = 'block';\n                notFoundElement.style.display = 'none';\n\n                const url = `https:\/\/web.jkchemical.com\/partial\/coaFileLotNumber\/${lot}`;\n                await fetch(url).then((res) =\u003e {\n                    if (res.status === 200) {\n                        window.open(url, '_blank');\n                    } else {\n                        notFoundElement.style.display = 'block';\n                    }\n                }).finally(() =\u003e {\n                    spinElement.style.display = 'none';\n                });\n            }\n        });\n    \u003c\/script\u003e\n\n\n\u003c\/div\u003e","brand":"US-Strem","offers":[{"title":"1×500mg","offer_id":45358228930750,"sku":"SC15-0488_500_MG","price":366.0,"currency_code":"USD","in_stock":true},{"title":"1×2g","offer_id":45358228963518,"sku":"SC15-0488_2_G","price":1244.0,"currency_code":"USD","in_stock":true},{"title":"1×10g","offer_id":45358228996286,"sku":"SC15-0488_10_G","price":4969.0,"currency_code":"USD","in_stock":true},{"title":"1×100mg","offer_id":45358229029054,"sku":"SC15-0488_100_MG","price":99.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0506\/0005\/0878\/files\/b3ebf60d243630e017d794af5764a102.jpg?v=1788907921"},{"product_id":"q8815-0179","title":"(S)-(-)-2,2'-Bis(diphenylphosphino)-6,6'-dimethoxy-1,1'-biphenyl, min. 97%  (S)-MeO-BIPHEP | 133545-17-2","description":"\u003cstyle\u003e\n  \/* isQuote *\/\n  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border-collapse: collapse;\n    margin: 15px 0;\n  }\n\n  .html-area table th,\n  .html-area table td {\n    border: 1px solid #e0e0e0;\n    padding: 5px 8px;\n  }\n\n  @media (max-width: 600px) {\n    .section-row {\n      grid-template-columns: repeat(1, 1fr);\n    }\n\n    .section-row .row-key {\n      grid-column: 1 \/ 2;\n    }\n\n    .section-row .row-value {\n      grid-column: 1 \/ 2;\n    }\n\n    .hazard-grid {\n      grid-template-columns: repeat(2, 1fr);\n      gap: 0 20px;\n    }\n  }\n  \n\u003c\/style\u003e\n\n\u003cdiv class=\"section\"\u003e\n  \n\n    \u003c!-- Order Info --\u003e\n    \u003ch2 class=\"section-header\"\u003eProduct Information\u003c\/h2\u003e\n    \u003cdiv class=\"section-content\"\u003e\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eProduct Name\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e(S)-(-)-2,2'-Bis(diphenylphosphino)-6,6'-dimethoxy-1,1'-biphenyl, min. 97%  (S)-MeO-BIPHEP\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n        \n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eBrand Name\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003eUS-Strem\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eProduct Number\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e15-0179\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eCAS\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e133545-17-2\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n\n        \n\n        \n\n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eCertificate of Analysis (COA)​\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e\n                \u003cdiv class=\"coa-search-container\"\u003e\n                    \u003cinput id=\"coa-link-input\" type=\"text\" placeholder=\"Enter Lot No.\"\u003e\n                    \u003cbutton id=\"coa-search-button\"\u003e\n                        \u003cdiv class=\"coa-search-button-content\"\u003e\n                            \u003csvg class=\"search-spin\" xmlns=\"http:\/\/www.w3.org\/2000\/svg\" viewbox=\"0 0 200 200\"\u003e\u003cradialgradient id=\"a7\" cx=\".66\" fx=\".66\" cy=\".3125\" fy=\".3125\" gradienttransform=\"scale(1.5)\"\u003e\u003cstop offset=\"0\" stop-color=\"#FFFFFF\"\u003e\u003c\/stop\u003e\u003cstop offset=\".3\" stop-color=\"#FFFFFF\" stop-opacity=\".9\"\u003e\u003c\/stop\u003e\u003cstop offset=\".6\" stop-color=\"#FFFFFF\" stop-opacity=\".6\"\u003e\u003c\/stop\u003e\u003cstop offset=\".8\" stop-color=\"#FFFFFF\" stop-opacity=\".3\"\u003e\u003c\/stop\u003e\u003cstop offset=\"1\" stop-color=\"#FFFFFF\" stop-opacity=\"0\"\u003e\u003c\/stop\u003e\u003c\/radialgradient\u003e\u003ccircle transform-origin=\"center\" fill=\"none\" stroke=\"url(#a7)\" stroke-width=\"15\" stroke-linecap=\"round\" stroke-dasharray=\"200 1000\" stroke-dashoffset=\"0\" cx=\"100\" cy=\"100\" r=\"70\"\u003e\u003canimatetransform type=\"rotate\" attributename=\"transform\" calcmode=\"spline\" dur=\"2\" values=\"360;0\" keytimes=\"0;1\" keysplines=\"0 0 1 1\" repeatcount=\"indefinite\"\u003e\u003c\/animatetransform\u003e\u003c\/circle\u003e\u003ccircle transform-origin=\"center\" fill=\"none\" opacity=\".2\" stroke=\"#FFFFFF\" stroke-width=\"15\" stroke-linecap=\"round\" cx=\"100\" cy=\"100\" r=\"70\"\u003e\u003c\/circle\u003e\u003c\/svg\u003e\n                            \u003cspan\u003eSearch\u003c\/span\u003e\n                        \u003c\/div\u003e\n                    \u003c\/button\u003e\n                    \u003cspan class=\"coa-not-found\"\u003eCOA not found\u003c\/span\u003e\n                \u003c\/div\u003e\n            \u003c\/div\u003e\n        \u003c\/div\u003e\n\n    \u003c\/div\u003e\n\n    \u003c!-- General Info --\u003e\n    \n        \u003ch2 class=\"section-header\"\u003eGeneral Information\u003c\/h2\u003e\n        \u003cdiv class=\"section-content\"\u003e\n            \n\n            \n            \u003cdiv class=\"section-row\"\u003e\n                \u003cdiv class=\"row-key\"\u003ePubChem CID\u003c\/div\u003e\n                \u003cdiv class=\"row-value\"\u003e4246603\u003c\/div\u003e\n            \u003c\/div\u003e\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eIUPAC Name\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003e\n\u003cspan class=\"l_bracket\"\u003e\u003c\/span\u003e2-(2-diphenylphosphanyl-6-methoxyphenyl)-3-methoxyphenyl\u003cspan class=\"r_bracket\"\u003e\u003c\/span\u003e-diphenylphosphane\u003c\/div\u003e\n                \u003c\/div\u003e\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eInChI Key\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003eKRJVQCZJJSUHHO-UHFFFAOYSA-N\u003c\/div\u003e\n                \u003c\/div\u003e\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eSMILES\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003eCOC1=C(C(=CC=C1)P(C2=CC=CC=C2)C3=CC=CC=C3)C4=C(C=CC=C4P(C5=CC=CC=C5)C6=CC=CC=C6)OC\u003c\/div\u003e\n                \u003c\/div\u003e\n            \n        \u003c\/div\u003e\n    \n\n    \u003c!-- Properties --\u003e\n    \n\n    \u003c!-- Safety Info --\u003e\n    \n\n    \u003c!-- Description --\u003e\n    \n    \u003ch2 class=\"section-header\"\u003eDescription\u003c\/h2\u003e\n    \u003cdiv class=\"html-area\"\u003e\n        Technical Note：\r1. See 15-0042.\u003cbr\u003e2.Ru and Ir catalyzed dynamic kinetic resolution for the synthesis of hydroxy, amino acid derivatives .\u003cbr\u003e3.Ru-catalyzed asymmetric hydrogenation of ketones and alkenes.\u003cbr\u003e4. Ir catalyzed enantioselective hydrogenation of heteroaromatic compounds.\u003cbr\u003e5.Conjugate addition using 2-heteroaryl titanates and zinc reagents.\u003cbr\u003e6.Enantio- and regiose lective heck-type reaction of aryl boronic acids with 2,3-dihydrofuran Rhodium-catalyzed carboncyl Z-dienylation.\u003cbr\u003eReferences:\u003cbr\u003e1.Adv. Synth. Catal., 2004, 346, 842.\u003cbr\u003e2.Org. L ett., 2006, 8, 4573.\u003cbr\u003e3.Org. Process Res. Devel., 2001, 5, 438\u003cbr\u003e4. J. Am. Chem. Soc., 2003, 125, 10536.\u003cbr\u003e5.Org. L ett., 2009, 1 1, 4200.\u003cbr\u003e6.J. Org. Chem. 2007, 72 , 3875.\u003cbr\u003e7. J. Am. Chem. Soc. 2006, 128, 16040.\n    \u003c\/div\u003e\n    \n\n    \u003c!-- Faq --\u003e\n    \n\n    \u003c!-- References --\u003e\n    \n    \u003ch2 class=\"section-header\"\u003e\n        \u003cspan style=\"display: block;\"\u003eReferences\u003c\/span\u003e\n        \u003cspan style=\"display: block; font-size: 1.2rem; color: #777; font-weight: lighter;\"\u003eData Source From Pubchem\u003c\/span\u003e\n    \u003c\/h2\u003e\n    \u003cdiv class=\"section-content\"\u003e\n        \n            \u003cdiv class=\"reference-item\"\u003e\n                \n                    \n                    \u003ca href=\"https:\/\/doi.org\/10.1038\/s44160-025-00839-y\" target=\"_blank\" rel=\"noopener noreferrer\"\u003e\n                        \u003ch3\u003eStrain-dependent enantioselectivity in mechanochemically coupled catalytic hydrogenation\u003c\/h3\u003e\n                    \u003c\/a\u003e\n                    \n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Name: Nature Synthesis\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Date: 2025-07-17\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003eDOI: 10.1038\/s44160-025-00839-y\u003c\/div\u003e\n                \n            \u003c\/div\u003e\n        \n            \u003cdiv class=\"reference-item\"\u003e\n                \n                    \n                    \u003ca href=\"https:\/\/doi.org\/10.1038\/s44160-024-00604-7\" target=\"_blank\" rel=\"noopener noreferrer\"\u003e\n                        \u003ch3\u003eRh-catalysed enantioselective [2+2+1] cycloaddition reactions using three different 2π-components\u003c\/h3\u003e\n                    \u003c\/a\u003e\n                    \n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Name: Nature Synthesis\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Date: 2024-07-17\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003eDOI: 10.1038\/s44160-024-00604-7\u003c\/div\u003e\n                \n            \u003c\/div\u003e\n        \n            \u003cdiv class=\"reference-item\"\u003e\n                \n                    \n                    \u003ca href=\"https:\/\/doi.org\/10.1038\/s44160-024-00555-z\" target=\"_blank\" rel=\"noopener noreferrer\"\u003e\n                        \u003ch3\u003eIntermolecular asymmetric functionalization of unstrained C(sp3)–C(sp3) bonds in allylic substitution reactions\u003c\/h3\u003e\n                    \u003c\/a\u003e\n                    \n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Name: Nature Synthesis\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Date: 2024-06-03\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003eDOI: 10.1038\/s44160-024-00555-z\u003c\/div\u003e\n                \n            \u003c\/div\u003e\n        \n            \u003cdiv class=\"reference-item\"\u003e\n                \n                    \n                    \u003ca href=\"https:\/\/science-of-synthesis.thieme.com\/app\/text\/?id=SD-120-00331\" target=\"_blank\" rel=\"noopener noreferrer\"\u003e\n                        \u003ch3\u003eCarboxylation of Alkyl Esters\u003c\/h3\u003e\n                    \u003c\/a\u003e\n                    \n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Name: Science of Synthesis\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Date: 2024\u003c\/div\u003e\n                \n\n                \n            \u003c\/div\u003e\n        \n            \u003cdiv class=\"reference-item\"\u003e\n                \n                    \n                    \u003ca href=\"https:\/\/doi.org\/10.1007\/s11426-023-1552-0\" target=\"_blank\" rel=\"noopener noreferrer\"\u003e\n                        \u003ch3\u003eCatalytic enantioselective domino alkenylation-alkynylation of alkenes: stereoselective synthesis of 5–7 membered azacycles and carbocycles\u003c\/h3\u003e\n                    \u003c\/a\u003e\n                    \n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Name: Science China Chemistry\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Date: 2023-04-10\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003eDOI: 10.1007\/s11426-023-1552-0\u003c\/div\u003e\n                \n            \u003c\/div\u003e\n        \n    \u003c\/div\u003e\n    \n\n\n    \u003cscript\u003e\n        const coaSearchButton = document.getElementById('coa-search-button');\n        coaSearchButton.addEventListener('click', async function() {\n            const coaLinkInput = document.getElementById('coa-link-input');\n            const spinElement = document.querySelector('.search-spin');\n            const notFoundElement = document.querySelector('.coa-not-found');\n\n            const lot = coaLinkInput.value.trim().toUpperCase();\n            if (lot.length \u003e 0) {\n                spinElement.style.display = 'block';\n                notFoundElement.style.display = 'none';\n\n                const url = `https:\/\/web.jkchemical.com\/partial\/coaFileLotNumber\/${lot}`;\n                await fetch(url).then((res) =\u003e {\n                    if (res.status === 200) {\n                        window.open(url, '_blank');\n                    } else {\n                        notFoundElement.style.display = 'block';\n                    }\n                }).finally(() =\u003e {\n                    spinElement.style.display = 'none';\n                });\n            }\n        });\n    \u003c\/script\u003e\n\n\n\u003c\/div\u003e","brand":"US-Strem","offers":[{"title":"1×100mg","offer_id":45358229127358,"sku":"SC15-0179_100_MG","price":99.0,"currency_code":"USD","in_stock":true},{"title":"1×10g","offer_id":45358229160126,"sku":"SC15-0179_10_G","price":4969.0,"currency_code":"USD","in_stock":true},{"title":"1×500mg","offer_id":45358229192894,"sku":"SC15-0179_500_MG","price":366.0,"currency_code":"USD","in_stock":true},{"title":"1×2g","offer_id":45358229225662,"sku":"SC15-0179_2_G","price":1244.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0506\/0005\/0878\/files\/0cd74442f7aabb1fdf879db608a8af98.jpg?v=1788908230"},{"product_id":"q8815-0113","title":"(S)-(-)-2,2'-Bis(di-2-furanylphosphino)-6,6'-dimethoxy-1,1'-biphenyl, min. 97% | 145214-59-1","description":"\u003cstyle\u003e\n  \/* isQuote *\/\n  div.swatch.clearfix {\n    display:  unset ;\n  }\n\n  \/* Hide sku *\/\n  .product-sku, \n  #leadtimetext {\n    display: none 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5px 8px;\n  }\n\n  @media (max-width: 600px) {\n    .section-row {\n      grid-template-columns: repeat(1, 1fr);\n    }\n\n    .section-row .row-key {\n      grid-column: 1 \/ 2;\n    }\n\n    .section-row .row-value {\n      grid-column: 1 \/ 2;\n    }\n\n    .hazard-grid {\n      grid-template-columns: repeat(2, 1fr);\n      gap: 0 20px;\n    }\n  }\n  \n\u003c\/style\u003e\n\n\u003cdiv class=\"section\"\u003e\n  \n\n    \u003c!-- Order Info --\u003e\n    \u003ch2 class=\"section-header\"\u003eProduct Information\u003c\/h2\u003e\n    \u003cdiv class=\"section-content\"\u003e\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eProduct Name\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e(S)-(-)-2,2'-Bis(di-2-furanylphosphino)-6,6'-dimethoxy-1,1'-biphenyl, min. 97%\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n        \n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eBrand Name\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003eUS-Strem\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eProduct Number\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e15-0113\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eCAS\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e145214-59-1\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n\n        \n\n        \n\n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eCertificate of Analysis (COA)​\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e\n                \u003cdiv class=\"coa-search-container\"\u003e\n                    \u003cinput id=\"coa-link-input\" type=\"text\" placeholder=\"Enter Lot No.\"\u003e\n                    \u003cbutton id=\"coa-search-button\"\u003e\n                        \u003cdiv class=\"coa-search-button-content\"\u003e\n                            \u003csvg class=\"search-spin\" xmlns=\"http:\/\/www.w3.org\/2000\/svg\" viewbox=\"0 0 200 200\"\u003e\u003cradialgradient id=\"a7\" cx=\".66\" fx=\".66\" cy=\".3125\" fy=\".3125\" gradienttransform=\"scale(1.5)\"\u003e\u003cstop offset=\"0\" stop-color=\"#FFFFFF\"\u003e\u003c\/stop\u003e\u003cstop offset=\".3\" stop-color=\"#FFFFFF\" stop-opacity=\".9\"\u003e\u003c\/stop\u003e\u003cstop offset=\".6\" stop-color=\"#FFFFFF\" stop-opacity=\".6\"\u003e\u003c\/stop\u003e\u003cstop offset=\".8\" stop-color=\"#FFFFFF\" stop-opacity=\".3\"\u003e\u003c\/stop\u003e\u003cstop offset=\"1\" stop-color=\"#FFFFFF\" stop-opacity=\"0\"\u003e\u003c\/stop\u003e\u003c\/radialgradient\u003e\u003ccircle transform-origin=\"center\" fill=\"none\" stroke=\"url(#a7)\" stroke-width=\"15\" stroke-linecap=\"round\" stroke-dasharray=\"200 1000\" stroke-dashoffset=\"0\" cx=\"100\" cy=\"100\" r=\"70\"\u003e\u003canimatetransform type=\"rotate\" attributename=\"transform\" calcmode=\"spline\" dur=\"2\" values=\"360;0\" keytimes=\"0;1\" keysplines=\"0 0 1 1\" repeatcount=\"indefinite\"\u003e\u003c\/animatetransform\u003e\u003c\/circle\u003e\u003ccircle transform-origin=\"center\" fill=\"none\" opacity=\".2\" stroke=\"#FFFFFF\" stroke-width=\"15\" stroke-linecap=\"round\" cx=\"100\" cy=\"100\" r=\"70\"\u003e\u003c\/circle\u003e\u003c\/svg\u003e\n                            \u003cspan\u003eSearch\u003c\/span\u003e\n                        \u003c\/div\u003e\n                    \u003c\/button\u003e\n                    \u003cspan class=\"coa-not-found\"\u003eCOA not found\u003c\/span\u003e\n                \u003c\/div\u003e\n            \u003c\/div\u003e\n        \u003c\/div\u003e\n\n    \u003c\/div\u003e\n\n    \u003c!-- General Info --\u003e\n    \n        \u003ch2 class=\"section-header\"\u003eGeneral Information\u003c\/h2\u003e\n        \u003cdiv class=\"section-content\"\u003e\n            \n\n            \n            \u003cdiv class=\"section-row\"\u003e\n                \u003cdiv class=\"row-key\"\u003ePubChem CID\u003c\/div\u003e\n                \u003cdiv class=\"row-value\"\u003e15307805\u003c\/div\u003e\n            \u003c\/div\u003e\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eIUPAC Name\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003e\n\u003cspan class=\"l_bracket\"\u003e\u003c\/span\u003e2-\u003cspan class=\"l_bracket\"\u003e\u003c\/span\u003e2-\u003cspan class=\"l_bracket\"\u003e\u003c\/span\u003ebis(furan-2-yl)phosphanyl\u003cspan class=\"r_bracket\"\u003e\u003c\/span\u003e-6-methoxyphenyl\u003cspan class=\"r_bracket\"\u003e\u003c\/span\u003e-3-methoxyphenyl\u003cspan class=\"r_bracket\"\u003e\u003c\/span\u003e-bis(furan-2-yl)phosphane\u003c\/div\u003e\n                \u003c\/div\u003e\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eInChI Key\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003eABGYJVGTLXSMBM-UHFFFAOYSA-N\u003c\/div\u003e\n                \u003c\/div\u003e\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eSMILES\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003eCOC1=C(C(=CC=C1)P(C2=CC=CO2)C3=CC=CO3)C4=C(C=CC=C4P(C5=CC=CO5)C6=CC=CO6)OC\u003c\/div\u003e\n                \u003c\/div\u003e\n            \n        \u003c\/div\u003e\n    \n\n    \u003c!-- Properties --\u003e\n    \n\n    \u003c!-- Safety Info --\u003e\n    \n        \u003ch2 class=\"section-header\"\u003eSafety Information\u003c\/h2\u003e\n        \u003cdiv class=\"section-content\"\u003e\n            \n\n            \n\n            \n\n            \n\n            \n\n            \n\n            \n\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eStorage Condition\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003e\n                        Store at 2-8℃\n                    \u003c\/div\u003e\n                \u003c\/div\u003e\n            \n        \u003c\/div\u003e\n    \n\n    \u003c!-- Description --\u003e\n    \n    \u003ch2 class=\"section-header\"\u003eDescription\u003c\/h2\u003e\n    \u003cdiv class=\"html-area\"\u003e\n        Technical Notes:\u003cbr\u003e1. Stereocontrol in palladium-catalyzed propargylic substitutions: kinetc resolution to give enantioenriched 1, 5- enynes and proaprgyl acetates\r2.Study of enantioselective catalysis of nitroso -Diels Alder reaction on solid support.\u003cbr\u003eReferences:\u003cbr\u003e1. Adv. Synth. Catal., 2013, 355, 3413. 2. Chem. Select, 201 7, 2, 3987.\n    \u003c\/div\u003e\n    \n\n    \u003c!-- Faq --\u003e\n    \n\n    \u003c!-- References --\u003e\n    \n    \u003ch2 class=\"section-header\"\u003e\n        \u003cspan style=\"display: block;\"\u003eReferences\u003c\/span\u003e\n        \u003cspan style=\"display: block; font-size: 1.2rem; color: #777; font-weight: lighter;\"\u003eData Source From Pubchem\u003c\/span\u003e\n    \u003c\/h2\u003e\n    \u003cdiv class=\"section-content\"\u003e\n        \n            \u003cdiv class=\"reference-item\"\u003e\n                \n                    \n                    \u003ca href=\"https:\/\/doi.org\/10.1055\/s-0040-1707160\" target=\"_blank\" rel=\"noopener noreferrer\"\u003e\n                        \u003ch3\u003eRecent Advances of 1,3,5-Triazinanes in Aminomethylation and Cycloaddition Reactions\u003c\/h3\u003e\n                    \u003c\/a\u003e\n                    \n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Name: Synthesis\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Date: 2020-07-06\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003eDOI: 10.1055\/s-0040-1707160\u003c\/div\u003e\n                \n            \u003c\/div\u003e\n        \n            \u003cdiv class=\"reference-item\"\u003e\n                \n                    \n                    \u003ca href=\"https:\/\/doi.org\/10.1055\/s-0039-1690490\" target=\"_blank\" rel=\"noopener noreferrer\"\u003e\n                        \u003ch3\u003eSynthesis of a CGRP Receptor Antagonist\u003c\/h3\u003e\n                    \u003c\/a\u003e\n                    \n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Name: Synfacts\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Date: 2019-08-20\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003eDOI: 10.1055\/s-0039-1690490\u003c\/div\u003e\n                \n            \u003c\/div\u003e\n        \n    \u003c\/div\u003e\n    \n\n\n    \u003cscript\u003e\n        const coaSearchButton = document.getElementById('coa-search-button');\n        coaSearchButton.addEventListener('click', async function() {\n            const coaLinkInput = document.getElementById('coa-link-input');\n            const spinElement = document.querySelector('.search-spin');\n            const notFoundElement = document.querySelector('.coa-not-found');\n\n            const lot = coaLinkInput.value.trim().toUpperCase();\n            if (lot.length \u003e 0) {\n                spinElement.style.display = 'block';\n                notFoundElement.style.display = 'none';\n\n                const url = `https:\/\/web.jkchemical.com\/partial\/coaFileLotNumber\/${lot}`;\n                await fetch(url).then((res) =\u003e {\n                    if (res.status === 200) {\n                        window.open(url, '_blank');\n                    } else {\n                        notFoundElement.style.display = 'block';\n                    }\n                }).finally(() =\u003e {\n                    spinElement.style.display = 'none';\n                });\n            }\n        });\n    \u003c\/script\u003e\n\n\n\u003c\/div\u003e","brand":"US-Strem","offers":[{"title":"1×2g","offer_id":45358230962366,"sku":"SC15-0113_2_G","price":1244.0,"currency_code":"USD","in_stock":true},{"title":"1×100mg","offer_id":45358230995134,"sku":"SC15-0113_100_MG","price":99.0,"currency_code":"USD","in_stock":true},{"title":"1×500mg","offer_id":45358231027902,"sku":"SC15-0113_500_MG","price":366.0,"currency_code":"USD","in_stock":true},{"title":"1×10g","offer_id":45358231060670,"sku":"SC15-0113_10_G","price":4969.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0506\/0005\/0878\/files\/acef79a8258498934c7a3d7b5194bd15.jpg?v=1788908328"},{"product_id":"q8815-0157","title":"(S)-(-)-2,2'-Bis(di-p-tolylphosphino)-6,6'-dimethoxy-1,1'-biphenyl, min. 97% | 133545-25-2","description":"\u003cstyle\u003e\n  \/* isQuote *\/\n  div.swatch.clearfix {\n    display:  unset ;\n  }\n\n  \/* Hide sku *\/\n  .product-sku, \n  #leadtimetext {\n    display: none !important;\n  }\n\n  \/* Square brackets *\/\n  span.l_bracket:before {\n    content: \"[\";\n  }\n  span.r_bracket:after {\n    content: \"]\";\n  }\n\n  \/* Hazard Symbols *\/\n  .ghs-symbols-row {\n    display: flex;\n    flex-wrap: wrap;\n    gap: 10px;\n  }\n\n  .hazard-symbol-container {\n    width: 50px;\n  }\n\n  .hazard-symbol {\n    object-fit: contain;\n    aspect-ratio: 1 \/ 1;\n    width: 100%;\n  }\n\n  \/* Section *\/\n  .section-header {\n    font-size: 2rem;\n    font-weight: bold;\n    color: #239ab7;\n    background-color: #f2f2f2;\n    padding: 10px;\n    border-radius: 4px;\n  }\n\n  .section-row {\n    display: grid;\n    grid-template-columns: repeat(8, 1fr);\n    padding: 6px 10px;\n    border-bottom: 1px solid #e0e0e0;\n  }\n\n  .section-content {\n    padding-bottom: 6px;\n  }\n\n  .section-content .section-row:last-child {\n    border-bottom: none;\n  }\n\n  .section-row .row-key {\n    grid-column: 1 \/ 3;\n    font-weight: bold;\n    align-self: center;\n  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5px 8px;\n  }\n\n  @media (max-width: 600px) {\n    .section-row {\n      grid-template-columns: repeat(1, 1fr);\n    }\n\n    .section-row .row-key {\n      grid-column: 1 \/ 2;\n    }\n\n    .section-row .row-value {\n      grid-column: 1 \/ 2;\n    }\n\n    .hazard-grid {\n      grid-template-columns: repeat(2, 1fr);\n      gap: 0 20px;\n    }\n  }\n  \n\u003c\/style\u003e\n\n\u003cdiv class=\"section\"\u003e\n  \n\n    \u003c!-- Order Info --\u003e\n    \u003ch2 class=\"section-header\"\u003eProduct Information\u003c\/h2\u003e\n    \u003cdiv class=\"section-content\"\u003e\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eProduct Name\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e(S)-(-)-2,2'-Bis(di-p-tolylphosphino)-6,6'-dimethoxy-1,1'-biphenyl, min. 97%\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n        \n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eBrand Name\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003eUS-Strem\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eProduct Number\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e15-0157\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eCAS\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e133545-25-2\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n\n        \n\n        \n\n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eCertificate of Analysis (COA)​\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e\n                \u003cdiv class=\"coa-search-container\"\u003e\n                    \u003cinput id=\"coa-link-input\" type=\"text\" placeholder=\"Enter Lot No.\"\u003e\n                    \u003cbutton id=\"coa-search-button\"\u003e\n                        \u003cdiv class=\"coa-search-button-content\"\u003e\n                            \u003csvg class=\"search-spin\" xmlns=\"http:\/\/www.w3.org\/2000\/svg\" viewbox=\"0 0 200 200\"\u003e\u003cradialgradient id=\"a7\" cx=\".66\" fx=\".66\" cy=\".3125\" fy=\".3125\" gradienttransform=\"scale(1.5)\"\u003e\u003cstop offset=\"0\" stop-color=\"#FFFFFF\"\u003e\u003c\/stop\u003e\u003cstop offset=\".3\" stop-color=\"#FFFFFF\" stop-opacity=\".9\"\u003e\u003c\/stop\u003e\u003cstop offset=\".6\" stop-color=\"#FFFFFF\" stop-opacity=\".6\"\u003e\u003c\/stop\u003e\u003cstop offset=\".8\" stop-color=\"#FFFFFF\" stop-opacity=\".3\"\u003e\u003c\/stop\u003e\u003cstop offset=\"1\" stop-color=\"#FFFFFF\" stop-opacity=\"0\"\u003e\u003c\/stop\u003e\u003c\/radialgradient\u003e\u003ccircle transform-origin=\"center\" fill=\"none\" stroke=\"url(#a7)\" stroke-width=\"15\" stroke-linecap=\"round\" stroke-dasharray=\"200 1000\" stroke-dashoffset=\"0\" cx=\"100\" cy=\"100\" r=\"70\"\u003e\u003canimatetransform type=\"rotate\" attributename=\"transform\" calcmode=\"spline\" dur=\"2\" values=\"360;0\" keytimes=\"0;1\" keysplines=\"0 0 1 1\" repeatcount=\"indefinite\"\u003e\u003c\/animatetransform\u003e\u003c\/circle\u003e\u003ccircle transform-origin=\"center\" fill=\"none\" opacity=\".2\" stroke=\"#FFFFFF\" stroke-width=\"15\" stroke-linecap=\"round\" cx=\"100\" cy=\"100\" r=\"70\"\u003e\u003c\/circle\u003e\u003c\/svg\u003e\n                            \u003cspan\u003eSearch\u003c\/span\u003e\n                        \u003c\/div\u003e\n                    \u003c\/button\u003e\n                    \u003cspan class=\"coa-not-found\"\u003eCOA not found\u003c\/span\u003e\n                \u003c\/div\u003e\n            \u003c\/div\u003e\n        \u003c\/div\u003e\n\n    \u003c\/div\u003e\n\n    \u003c!-- General Info --\u003e\n    \n        \u003ch2 class=\"section-header\"\u003eGeneral Information\u003c\/h2\u003e\n        \u003cdiv class=\"section-content\"\u003e\n            \n\n            \n            \u003cdiv class=\"section-row\"\u003e\n                \u003cdiv class=\"row-key\"\u003ePubChem CID\u003c\/div\u003e\n                \u003cdiv class=\"row-value\"\u003e22173705\u003c\/div\u003e\n            \u003c\/div\u003e\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eIUPAC Name\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003e\n\u003cspan class=\"l_bracket\"\u003e\u003c\/span\u003e2-\u003cspan class=\"l_bracket\"\u003e\u003c\/span\u003e2-bis(4-methylphenyl)phosphanyl-6-methoxyphenyl\u003cspan class=\"r_bracket\"\u003e\u003c\/span\u003e-3-methoxyphenyl\u003cspan class=\"r_bracket\"\u003e\u003c\/span\u003e-bis(4-methylphenyl)phosphane\u003c\/div\u003e\n                \u003c\/div\u003e\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eInChI Key\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003eDTMVLPFJTUJZAY-UHFFFAOYSA-N\u003c\/div\u003e\n                \u003c\/div\u003e\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eSMILES\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003eCC1=CC=C(C=C1)P(C2=CC=C(C=C2)C)C3=CC=CC(=C3C4=C(C=CC=C4P(C5=CC=C(C=C5)C)C6=CC=C(C=C6)C)OC)OC\u003c\/div\u003e\n                \u003c\/div\u003e\n            \n        \u003c\/div\u003e\n    \n\n    \u003c!-- Properties --\u003e\n    \n\n    \u003c!-- Safety Info --\u003e\n    \n\n    \u003c!-- Description --\u003e\n    \n    \u003ch2 class=\"section-header\"\u003eDescription\u003c\/h2\u003e\n    \u003cdiv class=\"html-area\"\u003e\n        Technical Note：\u003cbr\u003e1.See150042 \u003cbr\u003e2. Ru and Ir catalyzed dynamic kinetic res olution for the synthesis of hydroxy, amino acidderivatives\u003cbr\u003e3. Ru-catalyzed asymmetric hydrogenation of ketones and alkenes.\u003cbr\u003e4.lr catalyzed enantioselective hydrogenation of heteroaromatic compounds .\u003cbr\u003e5. Conjugate addition using 2-heteroaryl titanates and zinc reagents.\u003cbr\u003e6.Enantio- and regios elective heck-type reaction of aryl boronic acids with 2,3 dihydrofuran\u003cbr\u003e7.Rhodium-catalyzed carbonyl Z-dienylation.\u003cbr\u003e8.Rhodium-catalyzed asymmetric 1,4 addition of arylboronic acids to maleimides and enones .\u003cbr\u003eReferences:\u003cbr\u003e1.Adv. Synth. Catal., 2004, 346, 842.\u003cbr\u003e2.Org. L ett., 2006, 8, 4573.\u003cbr\u003e3.Org. Process Res. Devel., 2001, 5, 438.\u003cbr\u003e4.J. Am. Chem. Soc., 2003, 125, 10536.\u003cbr\u003e5.Org. L ett., 2009, 11, 4200.\u003cbr\u003e6.J .Org. Chem., 2007, 72 , 387 5.\u003cbr\u003e7.J. Am. C hem. Soc., 2006, 128, 1 6040.\u003cbr\u003e8.J. Org. Chem., 2011, 76, 6925.\n    \u003c\/div\u003e\n    \n\n    \u003c!-- Faq --\u003e\n    \n\n    \u003c!-- References --\u003e\n    \n\n\n    \u003cscript\u003e\n        const coaSearchButton = document.getElementById('coa-search-button');\n        coaSearchButton.addEventListener('click', async function() {\n            const coaLinkInput = document.getElementById('coa-link-input');\n            const spinElement = document.querySelector('.search-spin');\n            const notFoundElement = document.querySelector('.coa-not-found');\n\n            const lot = coaLinkInput.value.trim().toUpperCase();\n            if (lot.length \u003e 0) {\n                spinElement.style.display = 'block';\n                notFoundElement.style.display = 'none';\n\n                const url = `https:\/\/web.jkchemical.com\/partial\/coaFileLotNumber\/${lot}`;\n                await fetch(url).then((res) =\u003e {\n                    if (res.status === 200) {\n                        window.open(url, '_blank');\n                    } else {\n                        notFoundElement.style.display = 'block';\n                    }\n                }).finally(() =\u003e {\n                    spinElement.style.display = 'none';\n                });\n            }\n        });\n    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5px 8px;\n  }\n\n  @media (max-width: 600px) {\n    .section-row {\n      grid-template-columns: repeat(1, 1fr);\n    }\n\n    .section-row .row-key {\n      grid-column: 1 \/ 2;\n    }\n\n    .section-row .row-value {\n      grid-column: 1 \/ 2;\n    }\n\n    .hazard-grid {\n      grid-template-columns: repeat(2, 1fr);\n      gap: 0 20px;\n    }\n  }\n  \n\u003c\/style\u003e\n\n\u003cdiv class=\"section\"\u003e\n  \n\n    \u003c!-- Order Info --\u003e\n    \u003ch2 class=\"section-header\"\u003eProduct Information\u003c\/h2\u003e\n    \u003cdiv class=\"section-content\"\u003e\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eProduct Name\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e(R)-(+)-2,2'-Bis(di-i-propylphosphino)-6,6'-dimethoxy-1,1'-biphenyl, min. 97%\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n        \n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eBrand Name\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003eUS-Strem\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eProduct Number\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e15-0654\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eCAS\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e150971-45-2\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n\n        \n\n        \n\n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eCertificate of Analysis (COA)​\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e\n                \u003cdiv class=\"coa-search-container\"\u003e\n                    \u003cinput id=\"coa-link-input\" type=\"text\" placeholder=\"Enter Lot No.\"\u003e\n                    \u003cbutton id=\"coa-search-button\"\u003e\n                        \u003cdiv class=\"coa-search-button-content\"\u003e\n                            \u003csvg class=\"search-spin\" xmlns=\"http:\/\/www.w3.org\/2000\/svg\" viewbox=\"0 0 200 200\"\u003e\u003cradialgradient id=\"a7\" cx=\".66\" fx=\".66\" cy=\".3125\" fy=\".3125\" gradienttransform=\"scale(1.5)\"\u003e\u003cstop offset=\"0\" stop-color=\"#FFFFFF\"\u003e\u003c\/stop\u003e\u003cstop offset=\".3\" stop-color=\"#FFFFFF\" stop-opacity=\".9\"\u003e\u003c\/stop\u003e\u003cstop offset=\".6\" stop-color=\"#FFFFFF\" stop-opacity=\".6\"\u003e\u003c\/stop\u003e\u003cstop offset=\".8\" stop-color=\"#FFFFFF\" stop-opacity=\".3\"\u003e\u003c\/stop\u003e\u003cstop offset=\"1\" stop-color=\"#FFFFFF\" stop-opacity=\"0\"\u003e\u003c\/stop\u003e\u003c\/radialgradient\u003e\u003ccircle transform-origin=\"center\" fill=\"none\" stroke=\"url(#a7)\" stroke-width=\"15\" stroke-linecap=\"round\" stroke-dasharray=\"200 1000\" stroke-dashoffset=\"0\" cx=\"100\" cy=\"100\" r=\"70\"\u003e\u003canimatetransform type=\"rotate\" attributename=\"transform\" calcmode=\"spline\" dur=\"2\" values=\"360;0\" keytimes=\"0;1\" keysplines=\"0 0 1 1\" repeatcount=\"indefinite\"\u003e\u003c\/animatetransform\u003e\u003c\/circle\u003e\u003ccircle transform-origin=\"center\" fill=\"none\" opacity=\".2\" stroke=\"#FFFFFF\" stroke-width=\"15\" stroke-linecap=\"round\" cx=\"100\" cy=\"100\" r=\"70\"\u003e\u003c\/circle\u003e\u003c\/svg\u003e\n                            \u003cspan\u003eSearch\u003c\/span\u003e\n                        \u003c\/div\u003e\n                    \u003c\/button\u003e\n                    \u003cspan class=\"coa-not-found\"\u003eCOA not found\u003c\/span\u003e\n                \u003c\/div\u003e\n            \u003c\/div\u003e\n        \u003c\/div\u003e\n\n    \u003c\/div\u003e\n\n    \u003c!-- General Info --\u003e\n    \n        \u003ch2 class=\"section-header\"\u003eGeneral Information\u003c\/h2\u003e\n        \u003cdiv class=\"section-content\"\u003e\n            \n\n            \n            \u003cdiv class=\"section-row\"\u003e\n                \u003cdiv class=\"row-key\"\u003ePubChem CID\u003c\/div\u003e\n                \u003cdiv class=\"row-value\"\u003e15823035\u003c\/div\u003e\n            \u003c\/div\u003e\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eIUPAC Name\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003e\n\u003cspan class=\"l_bracket\"\u003e\u003c\/span\u003e2-\u003cspan class=\"l_bracket\"\u003e\u003c\/span\u003e2-di(propan-2-yl)phosphanyl-6-methoxyphenyl\u003cspan class=\"r_bracket\"\u003e\u003c\/span\u003e-3-methoxyphenyl\u003cspan class=\"r_bracket\"\u003e\u003c\/span\u003e-di(propan-2-yl)phosphane\u003c\/div\u003e\n                \u003c\/div\u003e\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eInChI Key\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003eHLLUWVKDDQIKNF-UHFFFAOYSA-N\u003c\/div\u003e\n                \u003c\/div\u003e\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eSMILES\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003eCC(C)P(C1=CC=CC(=C1C2=C(C=CC=C2P(C(C)C)C(C)C)OC)OC)C(C)C\u003c\/div\u003e\n                \u003c\/div\u003e\n            \n        \u003c\/div\u003e\n    \n\n    \u003c!-- Properties --\u003e\n    \n\n    \u003c!-- Safety Info --\u003e\n    \n\n    \u003c!-- Description --\u003e\n    \n    \u003ch2 class=\"section-header\"\u003eDescription\u003c\/h2\u003e\n    \u003cdiv class=\"html-area\"\u003e\n        Technical Notes:\u003cbr\u003eIn many respects the catalytic profile of the Me( BIPHEP ligands is similar to that of other atro binap and its many analogs. The nature of the PR2 group strongly influences the c atalytic perf ormar rhodium and ruthenium MeO-BIPHEP catalysts are highly effective for the hydrogenation of various several synthetically useful c-c coupling reactions.\u003cbr\u003e1. See 15-0042.\u003cbr\u003e2.Ru and Ir catalyzed dynamic kinetic resolution for the synthesis of hydroxy, amino acid derivatives .\u003cbr\u003e3. Ru-catalyzed asymmetric hydrogenation of ketones and alkenes .\u003cbr\u003e4.Ir catalyzed enantioselective hydrogenation of heteroaromatic compounds .\u003cbr\u003e5.Conjugate addition using 2-heteroaryl titanates and zinc reagents .\u003cbr\u003e6.Enantio- and regios elective heck-type reaction of aryl boronic acids with 2,3-dihydrofuran  \r7.Rhodium- catalyzed carbonyl Z-dienylation.\u003cbr\u003e8. Rhodium-catalyzed as ymmetric 1 ,4 addition of arylboronic acids to maleimides and enones .\n    \u003c\/div\u003e\n    \n\n    \u003c!-- Faq --\u003e\n    \n\n    \u003c!-- References --\u003e\n    \n    \u003ch2 class=\"section-header\"\u003e\n        \u003cspan style=\"display: block;\"\u003eReferences\u003c\/span\u003e\n        \u003cspan style=\"display: block; font-size: 1.2rem; color: #777; font-weight: lighter;\"\u003eData Source From Pubchem\u003c\/span\u003e\n    \u003c\/h2\u003e\n    \u003cdiv class=\"section-content\"\u003e\n        \n            \u003cdiv class=\"reference-item\"\u003e\n                \n                    \n                    \u003ca href=\"https:\/\/science-of-synthesis.thieme.com\/app\/text\/?id=SD-240-00112\" target=\"_blank\" rel=\"noopener noreferrer\"\u003e\n                        \u003ch3\u003eUsing Iridium Catalysis\u003c\/h3\u003e\n                    \u003c\/a\u003e\n                    \n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Name: Science of Synthesis\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Date: 2023\u003c\/div\u003e\n                \n\n                \n            \u003c\/div\u003e\n        \n            \u003cdiv class=\"reference-item\"\u003e\n                \n                    \n                    \u003ca href=\"https:\/\/doi.org\/10.1055\/s-0037-1610225\" target=\"_blank\" rel=\"noopener noreferrer\"\u003e\n                        \u003ch3\u003eCu-Catalyzed Conjugate Addition of Grignard Reagents to Thiochromones: An Enantioselective Pathway for Accessing 2-Alkylthiochromanones\u003c\/h3\u003e\n                    \u003c\/a\u003e\n                    \n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Name: Synlett\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Date: 2018-08-02\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003eDOI: 10.1055\/s-0037-1610225\u003c\/div\u003e\n                \n            \u003c\/div\u003e\n        \n            \u003cdiv class=\"reference-item\"\u003e\n                \n                    \n                    \u003ca href=\"https:\/\/doi.org\/10.1055\/s-0030-1260804\" target=\"_blank\" rel=\"noopener noreferrer\"\u003e\n                        \u003ch3\u003ePhosphine-Catalyzed [3+2] Annulation of Cyanoallenes\u003c\/h3\u003e\n                    \u003c\/a\u003e\n                    \n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Name: Synlett\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Date: 2011-06-21\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003eDOI: 10.1055\/s-0030-1260804\u003c\/div\u003e\n                \n            \u003c\/div\u003e\n        \n    \u003c\/div\u003e\n    \n\n\n    \u003cscript\u003e\n        const coaSearchButton = document.getElementById('coa-search-button');\n        coaSearchButton.addEventListener('click', async function() {\n            const coaLinkInput = document.getElementById('coa-link-input');\n            const spinElement = document.querySelector('.search-spin');\n            const notFoundElement = document.querySelector('.coa-not-found');\n\n            const lot = coaLinkInput.value.trim().toUpperCase();\n            if (lot.length \u003e 0) {\n                spinElement.style.display = 'block';\n                notFoundElement.style.display = 'none';\n\n                const url = `https:\/\/web.jkchemical.com\/partial\/coaFileLotNumber\/${lot}`;\n                await fetch(url).then((res) =\u003e {\n                    if (res.status === 200) {\n                        window.open(url, '_blank');\n                    } else {\n                        notFoundElement.style.display = 'block';\n                    }\n                }).finally(() =\u003e {\n                    spinElement.style.display = 'none';\n                });\n            }\n        });\n    \u003c\/script\u003e\n\n\n\u003c\/div\u003e","brand":"US-Strem","offers":[{"title":"1×500mg","offer_id":45358235418814,"sku":"SC15-0654_500_MG","price":366.0,"currency_code":"USD","in_stock":true},{"title":"1×2g","offer_id":45358235451582,"sku":"SC15-0654_2_G","price":1244.0,"currency_code":"USD","in_stock":true},{"title":"1×10g","offer_id":45358235484350,"sku":"SC15-0654_10_G","price":4969.0,"currency_code":"USD","in_stock":true},{"title":"1×100mg","offer_id":45358235517118,"sku":"SC15-0654_100_MG","price":99.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0506\/0005\/0878\/files\/ed8ec959198926c9ef761a4728837635.jpg?v=1788907809"},{"product_id":"q8815-1055","title":"(R)-(+)-5,5'-Dichloro-6,6'-dimethoxy-2,2'-bis(diphenyl­phosphino)-1,1'-biphenyl, min. 95% (R)-Cl-MeO-BIPHEP | 185913-97-7","description":"\u003cstyle\u003e\n  \/* isQuote *\/\n  div.swatch.clearfix {\n    display:  unset ;\n  }\n\n  \/* Hide sku *\/\n  .product-sku, \n  #leadtimetext {\n    display: none !important;\n  }\n\n  \/* Square brackets *\/\n  span.l_bracket:before {\n    content: \"[\";\n  }\n  span.r_bracket:after {\n    content: \"]\";\n  }\n\n  \/* Hazard Symbols *\/\n  .ghs-symbols-row {\n    display: flex;\n    flex-wrap: wrap;\n    gap: 10px;\n  }\n\n  .hazard-symbol-container {\n    width: 50px;\n  }\n\n  .hazard-symbol {\n    object-fit: contain;\n    aspect-ratio: 1 \/ 1;\n    width: 100%;\n  }\n\n  \/* Section *\/\n  .section-header {\n    font-size: 2rem;\n    font-weight: bold;\n    color: #239ab7;\n    background-color: #f2f2f2;\n    padding: 10px;\n    border-radius: 4px;\n  }\n\n  .section-row {\n    display: grid;\n    grid-template-columns: repeat(8, 1fr);\n    padding: 6px 10px;\n    border-bottom: 1px solid #e0e0e0;\n  }\n\n  .section-content {\n    padding-bottom: 6px;\n  }\n\n  .section-content .section-row:last-child {\n    border-bottom: none;\n  }\n\n  .section-row .row-key {\n    grid-column: 1 \/ 3;\n    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6px;\n  }\n\n  .section-row .coa-search-container input {\n    border: 1px solid #e0e0e0;\n    height: 2.5rem;\n    border-top-left-radius: 0.5rem !important;\n    border-bottom-left-radius: 0.5rem !important;\n    padding: 3px 5px;\n  }\n\n  .section-row .coa-search-container button {\n    height: 2.5rem;\n    line-height: 2.5rem;\n    border-radius: 0 0.5rem 0.5rem 0;\n  }\n\n  .section-row .coa-search-container button .coa-search-button-content {\n    display: flex;\n    align-items: center;\n    justify-content: center;\n    gap: 3px;\n  }\n\n  .section-row .coa-search-container button .coa-search-button-content .search-spin {\n    display: none;\n    width: 2rem;\n  }\n\n  .section-row .coa-search-container .coa-not-found {\n    display: none;\n    margin: 0 0 0 2rem;\n    color: #ad2031;\n    font-size: 1.3rem;\n  }\n\n  \/* Table *\/\n  .html-area table {\n    width: 100%;\n    border-collapse: collapse;\n    margin: 15px 0;\n  }\n\n  .html-area table th,\n  .html-area table td {\n    border: 1px solid #e0e0e0;\n    padding: 5px 8px;\n  }\n\n  @media (max-width: 600px) {\n    .section-row {\n      grid-template-columns: repeat(1, 1fr);\n    }\n\n    .section-row .row-key {\n      grid-column: 1 \/ 2;\n    }\n\n    .section-row .row-value {\n      grid-column: 1 \/ 2;\n    }\n\n    .hazard-grid {\n      grid-template-columns: repeat(2, 1fr);\n      gap: 0 20px;\n    }\n  }\n  \n\u003c\/style\u003e\n\n\u003cdiv class=\"section\"\u003e\n  \n\n    \u003c!-- Order Info --\u003e\n    \u003ch2 class=\"section-header\"\u003eProduct Information\u003c\/h2\u003e\n    \u003cdiv class=\"section-content\"\u003e\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eProduct Name\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e(R)-(+)-5,5'-Dichloro-6,6'-dimethoxy-2,2'-bis(diphenyl­phosphino)-1,1'-biphenyl, min. 95% (R)-Cl-MeO-BIPHEP\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n        \n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eBrand Name\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003eUS-Strem\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eProduct Number\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e15-1055\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eCAS\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e185913-97-7\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n\n        \n\n        \n\n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eCertificate of Analysis (COA)​\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e\n                \u003cdiv class=\"coa-search-container\"\u003e\n                    \u003cinput id=\"coa-link-input\" type=\"text\" placeholder=\"Enter Lot No.\"\u003e\n                    \u003cbutton id=\"coa-search-button\"\u003e\n                        \u003cdiv class=\"coa-search-button-content\"\u003e\n                            \u003csvg class=\"search-spin\" xmlns=\"http:\/\/www.w3.org\/2000\/svg\" viewbox=\"0 0 200 200\"\u003e\u003cradialgradient id=\"a7\" cx=\".66\" fx=\".66\" cy=\".3125\" fy=\".3125\" gradienttransform=\"scale(1.5)\"\u003e\u003cstop offset=\"0\" stop-color=\"#FFFFFF\"\u003e\u003c\/stop\u003e\u003cstop offset=\".3\" stop-color=\"#FFFFFF\" stop-opacity=\".9\"\u003e\u003c\/stop\u003e\u003cstop offset=\".6\" stop-color=\"#FFFFFF\" stop-opacity=\".6\"\u003e\u003c\/stop\u003e\u003cstop offset=\".8\" stop-color=\"#FFFFFF\" stop-opacity=\".3\"\u003e\u003c\/stop\u003e\u003cstop offset=\"1\" stop-color=\"#FFFFFF\" stop-opacity=\"0\"\u003e\u003c\/stop\u003e\u003c\/radialgradient\u003e\u003ccircle transform-origin=\"center\" fill=\"none\" stroke=\"url(#a7)\" stroke-width=\"15\" stroke-linecap=\"round\" stroke-dasharray=\"200 1000\" stroke-dashoffset=\"0\" cx=\"100\" cy=\"100\" r=\"70\"\u003e\u003canimatetransform type=\"rotate\" attributename=\"transform\" calcmode=\"spline\" dur=\"2\" values=\"360;0\" keytimes=\"0;1\" keysplines=\"0 0 1 1\" repeatcount=\"indefinite\"\u003e\u003c\/animatetransform\u003e\u003c\/circle\u003e\u003ccircle transform-origin=\"center\" fill=\"none\" opacity=\".2\" stroke=\"#FFFFFF\" stroke-width=\"15\" stroke-linecap=\"round\" cx=\"100\" cy=\"100\" r=\"70\"\u003e\u003c\/circle\u003e\u003c\/svg\u003e\n                            \u003cspan\u003eSearch\u003c\/span\u003e\n                        \u003c\/div\u003e\n                    \u003c\/button\u003e\n                    \u003cspan class=\"coa-not-found\"\u003eCOA not found\u003c\/span\u003e\n                \u003c\/div\u003e\n            \u003c\/div\u003e\n        \u003c\/div\u003e\n\n    \u003c\/div\u003e\n\n    \u003c!-- General Info --\u003e\n    \n        \u003ch2 class=\"section-header\"\u003eGeneral Information\u003c\/h2\u003e\n        \u003cdiv class=\"section-content\"\u003e\n            \n\n            \n            \u003cdiv class=\"section-row\"\u003e\n                \u003cdiv class=\"row-key\"\u003ePubChem CID\u003c\/div\u003e\n                \u003cdiv class=\"row-value\"\u003e5165044\u003c\/div\u003e\n            \u003c\/div\u003e\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eIUPAC Name\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003e\n\u003cspan class=\"l_bracket\"\u003e\u003c\/span\u003e4-chloro-2-(3-chloro-6-diphenylphosphanyl-2-methoxyphenyl)-3-methoxyphenyl\u003cspan class=\"r_bracket\"\u003e\u003c\/span\u003e-diphenylphosphane\u003c\/div\u003e\n                \u003c\/div\u003e\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eInChI Key\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003eGCBRCSSVOVNEIX-UHFFFAOYSA-N\u003c\/div\u003e\n                \u003c\/div\u003e\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eSMILES\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003eCOC1=C(C=CC(=C1C2=C(C=CC(=C2OC)Cl)P(C3=CC=CC=C3)C4=CC=CC=C4)P(C5=CC=CC=C5)C6=CC=CC=C6)Cl\u003c\/div\u003e\n                \u003c\/div\u003e\n            \n        \u003c\/div\u003e\n    \n\n    \u003c!-- Properties --\u003e\n    \n\n    \u003c!-- Safety Info --\u003e\n    \n\n    \u003c!-- Description --\u003e\n    \n    \u003ch2 class=\"section-header\"\u003eDescription\u003c\/h2\u003e\n    \u003cdiv class=\"html-area\"\u003e\n        Technical Notes:\u003cbr\u003e1. Ligand used in the ruthenium catalyzed, enantioselective hydrogenation of alkenes, carbonyls, and imines.\u003cbr\u003e2.Ligand used in the rhodium-catalyzed cyclization of acetylenic aldehydes.\u003cbr\u003e3.Ligand used in the iridium-catalyzed hydrogenative coupling of alkynes to aromatic and aliphatic N-arylsulfonyI aldimines.\u003cbr\u003e4. Asymmetric Cu-catalyzed propargylic substitution with amines,«a and enamines.\u003cbr\u003e5. Catalytic desymmetrizing intramolecular Heck reaction.\u003cbr\u003e6.Assembly of 1 ,3- polyols .\u003cbr\u003e7. Pd-catalyzed diastereo\/enantioselective allylic alkylations of ketone enolates .\u003cbr\u003e8. Enantioselective vinylogous Reformatsky-type addition.\u003cbr\u003e9. Cu-catalyzed chemoselective preparation of 2-(pinacolato)boron- substituted allylcopper complexes\u003cbr\u003eand their In situ site-, diastereo-, and enantioselective additions to ketones .\n    \u003c\/div\u003e\n    \n\n    \u003c!-- Faq --\u003e\n    \n\n    \u003c!-- References --\u003e\n    \n    \u003ch2 class=\"section-header\"\u003e\n        \u003cspan style=\"display: block;\"\u003eReferences\u003c\/span\u003e\n        \u003cspan style=\"display: block; font-size: 1.2rem; color: #777; font-weight: lighter;\"\u003eData Source From Pubchem\u003c\/span\u003e\n    \u003c\/h2\u003e\n    \u003cdiv class=\"section-content\"\u003e\n        \n            \u003cdiv class=\"reference-item\"\u003e\n                \n                    \n                    \u003ca href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC11087250\" target=\"_blank\" rel=\"noopener noreferrer\"\u003e\n                        \u003ch3\u003eChelation enables selectivity control in enantioconvergent Suzuki–Miyaura cross-couplings on acyclic allylic systems\u003c\/h3\u003e\n                    \u003c\/a\u003e\n                    \n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Name: Nature Chemistry\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Date: 2024-02-08\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003eDOI: 10.1038\/s41557-023-01430-8\u003c\/div\u003e\n                \n            \u003c\/div\u003e\n        \n            \u003cdiv class=\"reference-item\"\u003e\n                \n                    \n                    \u003ca href=\"https:\/\/science-of-synthesis.thieme.com\/app\/text\/?id=SD-147-00217\" target=\"_blank\" rel=\"noopener noreferrer\"\u003e\n                        \u003ch3\u003eSynthesis from Diynes and Ethyl Glyoxalate\u003c\/h3\u003e\n                    \u003c\/a\u003e\n                    \n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Name: Science of Synthesis\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Date: 2023\u003c\/div\u003e\n                \n\n                \n            \u003c\/div\u003e\n        \n            \u003cdiv class=\"reference-item\"\u003e\n                \n                    \n                    \u003ca href=\"https:\/\/science-of-synthesis.thieme.com\/app\/text\/?id=SD-147-00216\" target=\"_blank\" rel=\"noopener noreferrer\"\u003e\n                        \u003ch3\u003eSynthesis from Diynes and α-Oxo Aldehydes\u003c\/h3\u003e\n                    \u003c\/a\u003e\n                    \n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Name: Science of Synthesis\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Date: 2023\u003c\/div\u003e\n                \n\n                \n            \u003c\/div\u003e\n        \n            \u003cdiv class=\"reference-item\"\u003e\n                \n                    \n                    \u003ca href=\"https:\/\/doi.org\/10.1055\/s-0042-1753070\" target=\"_blank\" rel=\"noopener noreferrer\"\u003e\n                        \u003ch3\u003eEnantioselective Synthesis of Tetrahydrofurans via a Palladium-Catalyzed [3+2] Cycloaddition\u003c\/h3\u003e\n                    \u003c\/a\u003e\n                    \n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Name: Synfacts\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Date: 2022-11-17\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003eDOI: 10.1055\/s-0042-1753070\u003c\/div\u003e\n                \n            \u003c\/div\u003e\n        \n            \u003cdiv class=\"reference-item\"\u003e\n                \n                    \n                    \u003ca href=\"https:\/\/doi.org\/10.1055\/s-0041-1737859\" target=\"_blank\" rel=\"noopener noreferrer\"\u003e\n                        \u003ch3\u003eAsymmetric Propargylic Substitution Enabled by Synergistic Nickel and Chiral Anion Catalysis\u003c\/h3\u003e\n                    \u003c\/a\u003e\n                    \n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Name: Synfacts\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Date: 2022-02-16\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003eDOI: 10.1055\/s-0041-1737859\u003c\/div\u003e\n                \n            \u003c\/div\u003e\n        \n    \u003c\/div\u003e\n    \n\n\n    \u003cscript\u003e\n        const coaSearchButton = document.getElementById('coa-search-button');\n        coaSearchButton.addEventListener('click', async function() {\n            const coaLinkInput = document.getElementById('coa-link-input');\n            const spinElement = document.querySelector('.search-spin');\n            const notFoundElement = document.querySelector('.coa-not-found');\n\n            const lot = coaLinkInput.value.trim().toUpperCase();\n            if (lot.length \u003e 0) {\n                spinElement.style.display = 'block';\n                notFoundElement.style.display = 'none';\n\n                const url = `https:\/\/web.jkchemical.com\/partial\/coaFileLotNumber\/${lot}`;\n                await fetch(url).then((res) =\u003e {\n                    if (res.status === 200) {\n                        window.open(url, '_blank');\n                    } else {\n       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