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-90.933 L-18.215 -90.933"></path><path style="fill:none; stroke:black;" d="M-81.0272 0.3416 L-81.114 0.834 L-81.5838 1.005"></path><path style="fill:none; stroke:black;" d="M-98.503 -47.6726 L-98.886 -47.994 L-99.3559 -47.823"></path><path style="fill:none; stroke:black;" d="M-108.8352 10.923 L-109.305 11.094 L-109.688 10.7726"></path><path style="fill:none; stroke:black;" d="M-126.6071 -37.905 L-127.077 -37.734 L-127.1638 -37.2416"></path><path style="fill:none; stroke:black;" d="M-131.902 -7.8686 L-132.285 -8.19 L-132.1982 -8.6824"></path></g></g></svg></svg></svg></svg></div></app-svg-box></div></app-multi-image><h3 _ngcontent-sc115="" class="name">CAS Name</h3><span _ngcontent-sc115="" class="casName">Rociverine</span><h3 _ngcontent-sc115="" class="molecularFormula">Molecular Formula</h3><span _ngcontent-sc115="" id="molform">C<sub>20</sub>H<sub>37</sub>NO<sub>3</sub></span><h3 _ngcontent-sc115="" class="molecularMass">Molecular Mass</h3> 339.51 <button _ngcontent-sc115="" class="view-sfn-button">Discover more in SciFinder</button><div _ngcontent-sc115="" class="page-citation"><h3 _ngcontent-sc115="">Cite this Page</h3><span _ngcontent-sc115="" class="name">Rociverine</span>.   <em _ngcontent-sc115="">CAS Common Chemistry</em>.   CAS, a division of the American Chemical Society, n.d.   <span _ngcontent-sc115="" class="url">http://commonchemistry.cas.org/ChemicalDetail.aspx?ref=53716-44-2</span> (retrieved <span _ngcontent-sc115="" class="timestamp">2024-11-29</span>) (CAS RN: <span _ngcontent-sc115="" class="casRn">53716-44-2</span>).  Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0). </div></div></detail-summary></div><div _ngcontent-sc118="" class="col-lg-8 col-md-7 no-padding"><detail-ancillary _ngcontent-sc118="" _nghost-sc117=""><div _ngcontent-sc117="" class="detail-content-box detail-content-box-right"><h2 _ngcontent-sc117="" class="compoundPropertiesHeader">Compound Properties</h2><ul _ngcontent-sc117="" class="properties"><li _ngcontent-sc117=""><h3 _ngcontent-sc117="" class="property-name">Boiling Point (1)</h3><span _ngcontent-sc117="" class="property-value">149 °C</span></li></ul><h3 _ngcontent-sc117="">Source(s)</h3><ul _ngcontent-sc117="" class="sources"><li _ngcontent-sc117=""><span _ngcontent-sc117="">(1) PhysProp data were obtained from Syracuse Research Corporation of Syracuse, New York (US)</span></li></ul></div></detail-ancillary><detail-info _ngcontent-sc118="" _nghost-sc116=""><div _ngcontent-sc116="" class="detail-content-box detail-content-box-right"><h2 _ngcontent-sc116="">Other Names and Identifiers</h2><h3 _ngcontent-sc116="" class="inchi">InChI</h3><p _ngcontent-sc116="" class="identifier">InChI=1/C20H37NO3/c1-4-21(5-2)15-16(3)24-19(22)18-13-9-10-14-20(18,23)17-11-7-6-8-12-17/h16-18,23H,4-15H2,1-3H3/t16?,18-,20+/s2</p><h3 _ngcontent-sc116="" class="inchiKey">InChIKey</h3><p _ngcontent-sc116="" class="identifier">InChIKey=XPYLKZZOBVLVHB-FRWHHYCTNA-N</p><h3 _ngcontent-sc116="" class="smile">SMILES</h3><p _ngcontent-sc116="" class="identifier">O[C@]1([C@@H](C(OC(CN(CC)CC)C)=O)CCCC1)C2CCCCC2</p><h3 _ngcontent-sc116="" class="canonicalSmile">Canonical SMILES</h3><p _ngcontent-sc116="" class="identifier">O=C(OC(C)CN(CC)CC)C1CCCCC1(O)C2CCCCC2</p><h3 _ngcontent-sc116="" class="synonyms">Other Names for this Substance</h3><div _ngcontent-sc116="" class="detail-synonym-box"><ul _ngcontent-sc116=""><li _ngcontent-sc116="">[1,1′-Bicyclohexyl]-2-carboxylic acid, 1-hydroxy-, 2-(diethylamino)-1-methylethyl ester, (1<em>R</em>,2<em>R</em>)-<em>rel</em>-</li><li _ngcontent-sc116="">[1,1′-Bicyclohexyl]-2-carboxylic acid, 1-hydroxy-, 2-(diethylamino)-1-methylethyl ester, (1α,2α)-[<em>partial</em>]-</li><li _ngcontent-sc116="">Rociverine</li><li _ngcontent-sc116="">Rilaten</li><li _ngcontent-sc116="">LG 30158</li></ul></div><p _ngcontent-sc116=""></p></div></detail-info></div></div><div _ngcontent-sc118="" class="insight-teaser"><app-insight-teaser 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Chemistry is provided under the <a _ngcontent-sc106="" href="//creativecommons.org/licenses/by-nc/4.0/" target="_blank">Creative Commons CC BY-NC 4.0 license</a>. By using CAS Common Chemistry, you agree to the terms and conditions of this license. </div></app-license></div></div><ngx-json-ld _ngcontent-sc118=""><script type="application/ld+json">{ "@context": "http://schema.org", "@type": "ChemicalSubstance", "name": "Rociverine", "url": "http://commonchemistry.cas.org/ChemicalDetail.aspx?ref=53716-44-2", "hasBioChemEntityPart": { "@type": "MolecularEntity", "name": "Rociverine", "identifier": "InChI=1/C20H37NO3/c1-4-21(5-2)15-16(3)24-19(22)18-13-9-10-14-20(18,23)17-11-7-6-8-12-17/h16-18,23H,4-15H2,1-3H3/t16?,18-,20+/s2", "molecularFormula": "C<sub>20</sub>H<sub>37</sub>NO<sub>3</sub>" }, "chemicalComposition": "C<sub>20</sub>H<sub>37</sub>NO<sub>3</sub>", "alternateNames": [ "[1,1′-Bicyclohexyl]-2-carboxylic acid, 1-hydroxy-, 2-(diethylamino)-1-methylethyl ester, (1<em>R</em>,2<em>R</em>)-<em>rel</em>-", "[1,1′-Bicyclohexyl]-2-carboxylic acid, 1-hydroxy-, 2-(diethylamino)-1-methylethyl ester, (1α,2α)-[<em>partial</em>]-", "Rociverine", 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