{"product_id":"j5316571","title":"Boc-4-oxo-L-proline | 84348-37-8","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 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class=\"row-value\"\u003eBoc-4-oxo-L-proline\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\"\u003e16571\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\"\u003e84348-37-8\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\"\u003e11593804\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(2S)-1-\u003cspan class=\"l_bracket\"\u003e\u003c\/span\u003e(2-methylpropan-2-yl)oxycarbonyl\u003cspan class=\"r_bracket\"\u003e\u003c\/span\u003e-4-oxopyrrolidine-2-carboxylic 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\"\u003eCKYGSXRXTIKGAJ-ZETCQYMHSA-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)N1CC(=O)C\u003cspan class=\"l_bracket\"\u003e\u003c\/span\u003eC@H\u003cspan class=\"r_bracket\"\u003e\u003c\/span\u003e1C(=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-4-oxo-L-proline is widely utilized in research focused on:\u003c\/p\u003e\n\u003cp\u003ePeptide Synthesis: This compound serves as a valuable building block in the synthesis of peptides, particularly in the development of biologically active compounds. Its protective Boc (tert-butyloxycarbonyl) group allows for selective reactions, enhancing the efficiency of peptide assembly.\u003c\/p\u003e\n\u003cp\u003eDrug Development: In pharmaceutical research, Boc-4-oxo-L-proline is explored for its potential in creating novel drug candidates. Its unique structure can lead to compounds with improved efficacy and specificity, addressing unmet medical needs.\u003c\/p\u003e\n\u003cp\u003eBiochemical Studies: Researchers utilize this compound to study enzyme interactions and metabolic pathways. Its role in various biochemical processes helps in understanding disease mechanisms and developing targeted therapies.\u003c\/p\u003e\n\u003cp\u003eMaterial Science: The compound is investigated for its application in creating advanced materials, such as polymers and hydrogels, which can be used in drug delivery systems or tissue engineering, providing innovative solutions in medical technology.\u003c\/p\u003e\n\u003cp\u003eAnalytical Chemistry: Boc-4-oxo-L-proline is employed as a standard in analytical methods, aiding in the quantification of related compounds in complex mixtures, thus enhancing the accuracy of analytical results in various research fields.\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-0040-1707092\" target=\"_blank\" rel=\"noopener noreferrer\"\u003e\n                        \u003ch3\u003eSynthesis of (+)-Oxo-tomaymycin\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: 2020-07-21\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003eDOI: 10.1055\/s-0040-1707092\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-0037-1611672\" target=\"_blank\" rel=\"noopener noreferrer\"\u003e\n                        \u003ch3\u003eSynthesis of 4-(Arylmethyl)proline Derivatives\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: 2019-01-25\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003eDOI: 10.1055\/s-0037-1611672\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-0034-1380333\" target=\"_blank\" rel=\"noopener noreferrer\"\u003e\n                        \u003ch3\u003eSynthesis of an HCV Protease Inhibitor\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: 2015-03-18\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003eDOI: 10.1055\/s-0034-1380333\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\/12354018\" target=\"_blank\" rel=\"noopener noreferrer\"\u003e\n                        \u003ch3\u003ePractical Synthesis of Boc-Protected cis-4-Trifluoromethyl and cis-4-Difluoromethyl-l- prolines\u003c\/h3\u003e\n                    \u003c\/a\u003e\n                    \n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Name: The Journal of Organic Chemistry\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003ePublication Date: 2002-09-11\u003c\/div\u003e\n                \n\n                \n                \u003cdiv class=\"publication-item\"\u003eDOI: 10.1021\/jo0257400\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         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