{"product_id":"j5302896","title":"Boc-D-tyrosine | 70642-86-3","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 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class=\"row-value\"\u003eBoc-D-tyrosine\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\"\u003eChem Impex\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\"\u003e02896\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\"\u003e70642-86-3\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\"\u003e1549481\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(2R)-3-(4-hydroxyphenyl)-2-\u003cspan class=\"l_bracket\"\u003e\u003c\/span\u003e(2-methylpropan-2-yl)oxycarbonylamino\u003cspan class=\"r_bracket\"\u003e\u003c\/span\u003epropanoic acid\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\"\u003eCNBUSIJNWNXLQQ-LLVKDONJSA-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)OC(=O)N\u003cspan class=\"l_bracket\"\u003e\u003c\/span\u003eC@H\u003cspan class=\"r_bracket\"\u003e\u003c\/span\u003e(CC1=CC=C(C=C1)O)C(=O)O\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!-- Application  --\u003e\n    \n    \u003ch2 class=\"section-header\"\u003eApplication\u003c\/h2\u003e\n    \u003cdiv class=\"html-area\"\u003e\n        \u003cp\u003eBoc-D-tyrosine is widely utilized in research focused on:\u003c\/p\u003e\n\u003cp\u003ePeptide Synthesis: This compound serves as a protective group in the synthesis of peptides, allowing for the selective modification of amino acids without affecting the overall structure. This is particularly beneficial in pharmaceutical research where precise modifications are crucial.\u003c\/p\u003e\n\u003cp\u003eDrug Development: Boc-D-tyrosine is often used in the development of novel therapeutic agents, especially in creating compounds that target specific biological pathways. Its ability to enhance solubility can improve the bioavailability of drugs.\u003c\/p\u003e\n\u003cp\u003eBioconjugation: In bioconjugation applications, Boc-D-tyrosine can be utilized to link biomolecules, such as proteins and antibodies, to drug molecules, enhancing their therapeutic efficacy and targeting capabilities.\u003c\/p\u003e\n\u003cp\u003eResearch in Neuroscience: This compound is important in studies related to neurotransmitter systems, particularly in understanding the role of tyrosine derivatives in brain function and mental health.\u003c\/p\u003e\n\u003cp\u003eCosmetic Formulations: Due to its properties, Boc-D-tyrosine is also explored in cosmetic chemistry for formulating products that promote skin health, leveraging its antioxidant potential.\u003c\/p\u003e\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-0030-1260561\" target=\"_blank\" rel=\"noopener noreferrer\"\u003e\n                        \u003ch3\u003eA Rapid and Highly Diastereoselective Synthesis of Enantiomerically Pure (4R,5R)- and (4S,5S)-Isocytoxazone\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: 2011-05-13\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003eDOI: 10.1055\/s-0030-1260561\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\/17565485\" target=\"_blank\" rel=\"noopener noreferrer\"\u003e\n                        \u003ch3\u003eChiral effects of alkyl-substituted derivatives of N,O-bismethacryloyl ethanolamine on the performance of one monomer molecularly imprinted polymers (OMNiMIPs)\u003c\/h3\u003e\n                    \u003c\/a\u003e\n                    \n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Name: Analytical and Bioanalytical Chemistry\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Date: 2007-06-13\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003eDOI: 10.1007\/s00216-007-1364-2\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-2006-958931\" target=\"_blank\" rel=\"noopener noreferrer\"\u003e\n                        \u003ch3\u003eAn Effective Route to (-)-Aphanorphine Using d-Tyrosine as a Chiral Building Block\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: 2007-01\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003eDOI: 10.1055\/s-2006-958931\u003c\/div\u003e\n                \n            \u003c\/div\u003e\n        \n            \u003cdiv class=\"reference-item\"\u003e\n                \n                    \n                    \u003ca href=\"https:\/\/doi.org\/10.1007\/bf02789765\" target=\"_blank\" rel=\"noopener noreferrer\"\u003e\n                        \u003ch3\u003eThe effect of structure on the resolution of dansyl amino acids using beta-cyclodextrin as a mobile phase additive in reversed-phase thin-layer chromatography\u003c\/h3\u003e\n                    \u003c\/a\u003e\n                    \n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Name: Chromatographia\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Date: 2000-11\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003eDOI: 10.1007\/bf02789765\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\/8289198\" target=\"_blank\" rel=\"noopener noreferrer\"\u003e\n                        \u003ch3\u003eA recombinant human stromelysin catalytic domain identifying tryptophan derivatives as human stromelysin inhibitors\u003c\/h3\u003e\n                    \u003c\/a\u003e\n                    \n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Name: Journal of Medicinal Chemistry\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Date: 1994-01-07\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003eDOI: 10.1021\/jm00027a027\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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