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_ngcontent-sc103=""></router-outlet><app-detail _nghost-sc118=""><div _ngcontent-sc118="" class="centered-container"><!----><div _ngcontent-sc118="" class="main-content"><app-messages _ngcontent-sc118="" _nghost-sc111=""><!----></app-messages><!----><div _ngcontent-sc118="" class="col-lg-12 col-md-12 col-sm-12 col-xs-12 padding-bottom-40"><div _ngcontent-sc118="" class="row"><div _ngcontent-sc118="" class="col-lg-10 col-md-10 col-sm-10 col-xs-10 no-padding"><h1 _ngcontent-sc118="" class="detail-title">Dimethisterone</h1></div><div _ngcontent-sc118="" class="col-lg-2 col-md-2 col-sm-2 col-xs-2 no-padding"><app-detail-download-button _ngcontent-sc118="" _nghost-sc112=""><button _ngcontent-sc112="" aria-label="Download Substance Molfile" class="download-button"></button></app-detail-download-button></div></div><div _ngcontent-sc118="" class="col-lg-4 col-md-5 no-padding"><detail-summary _ngcontent-sc118="" _nghost-sc115=""><div _ngcontent-sc115="" class="detail-content-box 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_ngcontent-sc115="" class="casName">Dimethisterone</span><h3 _ngcontent-sc115="" class="molecularFormula">Molecular Formula</h3><!----><span _ngcontent-sc115="" id="molform">C<sub>23</sub>H<sub>32</sub>O<sub>2</sub></span><h3 _ngcontent-sc115="" class="molecularMass">Molecular Mass</h3><!----> 340.50 <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">Dimethisterone</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?cas_rn=79-64-1</span> (retrieved <span _ngcontent-sc115="" class="timestamp">2024-12-01</span>) (CAS RN: <span _ngcontent-sc115="" class="casRn">79-64-1</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">Melting Point (1)</h3><span _ngcontent-sc117="" class="property-value">102 °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=1S/C23H32O2/c1-5-9-23(25)12-8-19-17-13-15(2)20-14-16(24)6-10-21(20,3)18(17)7-11-22(19,23)4/h14-15,17-19,25H,6-8,10-13H2,1-4H3/t15-,17+,18-,19-,21+,22-,23-/m0/s1</p><h3 _ngcontent-sc116="" class="inchiKey">InChIKey</h3><!----><p _ngcontent-sc116="" class="identifier">InChIKey=LVHOURKCKUYIGK-RGUJTQARSA-N</p><h3 _ngcontent-sc116="" class="smile">SMILES</h3><!----><p _ngcontent-sc116="" class="identifier">C[C@@]12[C@]([C@]3([C@@]([C@]4(C)C([C@@H](C)C3)=CC(=O)CC4)(CC1)[H])[H])(CC[C@]2(C#CC)O)[H]</p><h3 _ngcontent-sc116="" class="canonicalSmile">Canonical SMILES</h3><!----><p _ngcontent-sc116="" class="identifier">O=C1C=C2C(C)CC3C(CCC4(C)C3CCC4(O)C#CC)C2(C)CC1</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="">Androst-4-en-3-one, 17-hydroxy-6-methyl-17-(1-propynyl)-, (6α,17β)-</li><li _ngcontent-sc116="">Androst-4-en-3-one, 17β-hydroxy-6α-methyl-17-(1-propynyl)-</li><li _ngcontent-sc116="">Testosterone, 6α-methyl-17-(1-propynyl)-</li><li _ngcontent-sc116="">(6α,17β)-17-Hydroxy-6-methyl-17-(1-propynyl)androst-4-en-3-one</li><li _ngcontent-sc116="">Dimethisterone</li><!----></ul><!----></div><div _ngcontent-sc116="" class="synonyms-toggle"><p _ngcontent-sc116=""><a _ngcontent-sc116="">View All</a></p></div><!----><h2 _ngcontent-sc116="" class="deletedOrReplacedRns">Deleted or Replaced CAS Registry Numbers</h2><!----><p _ngcontent-sc116="">28779-28-4, 68378-60-9, 1353032-53-7</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 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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": "Dimethisterone", "url": "http://commonchemistry.cas.org/detail?cas_rn=79-64-1", "hasBioChemEntityPart": { "@type": "MolecularEntity", "name": "Dimethisterone", "identifier": "InChI=1S/C23H32O2/c1-5-9-23(25)12-8-19-17-13-15(2)20-14-16(24)6-10-21(20,3)18(17)7-11-22(19,23)4/h14-15,17-19,25H,6-8,10-13H2,1-4H3/t15-,17+,18-,19-,21+,22-,23-/m0/s1", "molecularFormula": "C<sub>23</sub>H<sub>32</sub>O<sub>2</sub>" }, "chemicalComposition": "C<sub>23</sub>H<sub>32</sub>O<sub>2</sub>", "alternateNames": [ "Androst-4-en-3-one, 17-hydroxy-6-methyl-17-(1-propynyl)-, (6α,17β)-", "Androst-4-en-3-one, 17β-hydroxy-6α-methyl-17-(1-propynyl)-", "Testosterone, 6α-methyl-17-(1-propynyl)-", "(6α,17β)-17-Hydroxy-6-methyl-17-(1-propynyl)androst-4-en-3-one", "Dimethisterone", "6α,21-Dimethylethisterone", "6α,21-Dimethyl-17-ethynyl-17β-hydroxyandrost-4-en-3-one", "17β-Hydroxy-6α-methyl-17-(1-propynyl)androst-4-en-3-one", "Secrosteron", "6α-Methyl-17α-propynyltestosterone", "Dimethisteron", "Lutogan", "P-5048", "6α-Methyl-17-(1-propynyl)testosterone", "Dimethiderome", "MeSH ID: D004116" ] }</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" 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