Cas no 516-84-7 ((10S)-3c-Hydroxy-10r.13c-dimethyl-17c-((1R:4R)-1.4.5-trimethyl-hexen-(2t)-yl)-(5tH.14tH)-Delta7.9(11)-dodecahydro-1H-cyclopenta[a]phenanthren)
![(10S)-3c-Hydroxy-10r.13c-dimethyl-17c-((1R:4R)-1.4.5-trimethyl-hexen-(2t)-yl)-(5tH.14tH)-Delta7.9(11)-dodecahydro-1H-cyclopenta[a]phenanthren structure](https://ossimg.kuujia.com/scimg/1000/516-84-7x500.png)
516-84-7 structure
Product Name:(10S)-3c-Hydroxy-10r.13c-dimethyl-17c-((1R:4R)-1.4.5-trimethyl-hexen-(2t)-yl)-(5tH.14tH)-Delta7.9(11)-dodecahydro-1H-cyclopenta[a]phenanthren
CAS No:516-84-7
MF:C28H44O
MW:396.648368835449
CID:2034985
Update Time:2025-04-21
(10S)-3c-Hydroxy-10r.13c-dimethyl-17c-((1R:4R)-1.4.5-trimethyl-hexen-(2t)-yl)-(5tH.14tH)-Delta7.9(11)-dodecahydro-1H-cyclopenta[a]phenanthren Chemical and Physical Properties
Names and Identifiers
-
- (10S)-3c-Hydroxy-10r.13c-dimethyl-17c-((1R:4R)-1.4.5-trimethyl-hexen-(2t)-yl)-(5tH.14tH)-Delta7.9(11)-dodecahydro-1H-cyclopenta[a]phenanthren
- (24R)-24-Methyl-5alpha-cholestatrien-(7.9(11).22t)-ol-(3beta)
- 24betaF-Methyl-5alpha-cholestatrien-(7.9(11).22t)-ol-(3beta)
- 3beta-Hydroxy-10.13-dimethyl-17beta-((1R:4R)-1.4.5-trimethyl-hexen-(2t)-yl)-5alpha-gonadien-(7.9(11))
- 5alpha-ergostatrien-(7.9(11).22t)-ol-(3beta)
- ergosta-7,9(11),22-triene-3beta-ol
- ergosterol D
- (22E)-5α-Ergosta-7,9(11),22-trien-3β-ol
-
- Inchi： 1S/C28H44O/c1-18(2)19(3)7-8-20(4)24-11-12-25-23-10-9-21-17-22(29)13-15-27(21,5)26(23)14-16-28(24,25)6/h7-8,10,14,18-22,24-25,29H,9,11-13,15-17H2,1-6H3
- InChI Key： XSMGJKKUFBTARU-UHFFFAOYSA-N
- SMILES： CC(C(C=CC(C1C2(C(C3C(=CC2)C2(C(CC(CC2)O)CC=3)C)CC1)C)C)C)C
(10S)-3c-Hydroxy-10r.13c-dimethyl-17c-((1R:4R)-1.4.5-trimethyl-hexen-(2t)-yl)-(5tH.14tH)-Delta7.9(11)-dodecahydro-1H-cyclopenta[a]phenanthren Related Literature
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Inês S. Albuquerque,Hélia F. Jeremias,Miguel Chaves-Ferreira,Dijana Matak-Vinkovic,Omar Boutureira,Carlos C. Rom?o Chem. Commun., 2015,51, 3993-3996
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Bidou Wang,Xifeng Chen Analyst, 2014,139, 5695-5699
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Cheng Fang,Jinjian Wu,Zahra Sobhani,Md. Al Amin,Youhong Tang Anal. Methods, 2019,11, 163-170
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Juan J. Sánchez,Miguel López-Haro,Juan C. Hernández-Garrido,Ginesa Blanco,Miguel A. Cauqui,José M. Rodríguez-Izquierdo,José A. Pérez-Omil,José J. Calvino,María P. Yeste J. Mater. Chem. A, 2019,7, 8993-9003
Related Categories
- Solvents and Organic Chemicals Organic Compounds Lipids and lipid-like molecules Steroids and steroid derivatives Ergosterols and derivatives
- Solvents and Organic Chemicals Organic Compounds Lipids and lipid-like molecules Steroids and steroid derivatives Ergostane steroids Ergosterols and derivatives
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