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L-25.8832 -28.4575 Q-25.3207 -27.395 -25.3207 -26.1137 Z"></path><path style="fill:none; stroke:black;" d="M22.0656 -46.2292 L22.269 -46.686 L21.8974 -47.0206"></path><path style="fill:none; stroke:black;" d="M-25.9031 -51.2729 L-26.007 -51.762 L-25.574 -52.012"></path><path style="fill:none; stroke:black;" d="M0.3446 -66.4274 L-0.027 -66.762 L-0.46 -66.512"></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">(+)-Methyl jasmonate</span><h3 _ngcontent-sc115="" class="molecularFormula">Molecular Formula</h3><span _ngcontent-sc115="" id="molform">C<sub>13</sub>H<sub>20</sub>O<sub>3</sub></span><h3 _ngcontent-sc115="" class="molecularMass">Molecular Mass</h3> 224.30 <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">(+)-Methyl jasmonate</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/detail?ref=78609-06-0</span> (retrieved <span _ngcontent-sc115="" class="timestamp">2025-03-03</span>) (CAS RN: <span _ngcontent-sc115="" class="casRn">78609-06-0</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-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=1S/C13H20O3/c1-3-4-5-6-11-10(7-8-12(11)14)9-13(15)16-2/h4-5,10-11H,3,6-9H2,1-2H3/b5-4-/t10-,11-/m0/s1</p><h3 _ngcontent-sc116="" class="inchiKey">InChIKey</h3><p _ngcontent-sc116="" class="identifier">InChIKey=GEWDNTWNSAZUDX-XXJOZFEBSA-N</p><h3 _ngcontent-sc116="" class="smile">SMILES</h3><p _ngcontent-sc116="" class="identifier">C(C(OC)=O)[C@H]1[C@H](C/C=C\CC)C(=O)CC1</p><h3 _ngcontent-sc116="" class="canonicalSmile">Canonical SMILES</h3><p _ngcontent-sc116="" class="identifier">O=C(OC)CC1CCC(=O)C1CC=CCC</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="">Cyclopentaneacetic acid, 3-oxo-2-(2<em>Z</em>)-2-penten-1-yl-, methyl ester, (1<em>S</em>,2<em>S</em>)-</li><li _ngcontent-sc116="">Cyclopentaneacetic acid, 3-oxo-2-(2-pentenyl)-, methyl ester, [1<em>S</em>-[1α,2β(<em>Z</em>)]]-</li><li _ngcontent-sc116="">Cyclopentaneacetic acid, 3-oxo-2-(2<em>Z</em>)-2-pentenyl-, methyl ester, (1<em>S</em>,2<em>S</em>)-</li><li _ngcontent-sc116="">(+)-Methyl jasmonate</li><li _ngcontent-sc116="">(+)-Jasmonic acid methyl ester</li></ul></div><div _ngcontent-sc116="" class="synonyms-toggle"><p _ngcontent-sc116=""><a _ngcontent-sc116="">View All</a></p></div><p _ngcontent-sc116=""></p></div></detail-info></div></div><div _ngcontent-sc118="" class="insight-teaser"><app-insight-teaser _ngcontent-sc118="" _nghost-sc107=""><div _ngcontent-sc107="" class="row teaser-header cas-blue">CAS INSIGHTS<sup _ngcontent-sc107="">TM</sup></div><div _ngcontent-sc107="" class="teaser-container"><div _ngcontent-sc107="" class="teaser text-black"><div _ngcontent-sc107="" class="teaser-img"><a _ngcontent-sc107="" target="_blank" class="insight-teaser-link" href="https://www.cas.org/resources/topic/emerging-science?utm_campaign=GLO_GEN_ANY_CIS_AWS&utm_medium=SYN_CAS_ORG&utm_source=CommonChemistry"><img _ngcontent-sc107="" 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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": "(+)-Methyl jasmonate", "url": "http://commonchemistry.cas.org/detail?ref=78609-06-0", "hasBioChemEntityPart": { "@type": "MolecularEntity", "name": "(+)-Methyl jasmonate", "identifier": "InChI=1S/C13H20O3/c1-3-4-5-6-11-10(7-8-12(11)14)9-13(15)16-2/h4-5,10-11H,3,6-9H2,1-2H3/b5-4-/t10-,11-/m0/s1", "molecularFormula": "C<sub>13</sub>H<sub>20</sub>O<sub>3</sub>" }, "chemicalComposition": "C<sub>13</sub>H<sub>20</sub>O<sub>3</sub>", "alternateNames": [ "Cyclopentaneacetic acid, 3-oxo-2-(2<em>Z</em>)-2-penten-1-yl-, methyl ester, (1<em>S</em>,2<em>S</em>)-", "Cyclopentaneacetic acid, 3-oxo-2-(2-pentenyl)-, methyl ester, [1<em>S</em>-[1α,2β(<em>Z</em>)]]-", "Cyclopentaneacetic acid, 3-oxo-2-(2<em>Z</em>)-2-pentenyl-, methyl ester, (1<em>S</em>,2<em>S</em>)-", "(+)-Methyl jasmonate", "(+)-Jasmonic acid methyl ester", "(3S,7S)-Methyl jasmonate" ] }</script></ngx-json-ld></app-detail><app-footer _ngcontent-sc103="" _nghost-sc102=""><div _ngcontent-sc102="" class="footer-container"><div _ngcontent-sc102="" class="centered-container"><div _ngcontent-sc102="" class="site-footer__nav site-footer"><ul _ngcontent-sc102="" class="site-footer__menu site-footer--level-1 site-footer__menu--mega"><li _ngcontent-sc102="" class="site-footer__item site-footer__item--level-1 site-footer__item--has-children"><h2 _ngcontent-sc102="" class="heading is-style-h5"><a _ngcontent-sc102="" href="https://www.cas.org/cas-solutions" target="_blank" class="site-footer__link site-footer__link--level-1">Solutions</a></h2><ul _ngcontent-sc102="" class="site-footer__sub-menu site-footer--level-2 site-footer__menu--mega"><li _ngcontent-sc102="" class="site-footer__item site-footer__item--level-2"><a _ngcontent-sc102="" 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