(3-BETA,20S,23Z)-3,20-DIHYDROXY-21-METHOXY-24-[(2-METHOXY-PHENYL)-THIO]-24-(TRIMETHYLSILYL)-5-BETA-CHOL-23-ENE
Compound with spectra: 1 NMR
![(3-BETA,20S,23Z)-3,20-DIHYDROXY-21-METHOXY-24-[(2-METHOXY-PHENYL)-THIO]-24-(TRIMETHYLSILYL)-5-BETA-CHOL-23-ENE](/api/compound/IiuPU8rZj3k.png?ph=true&h=300&w=458 "(3-BETA,20S,23Z)-3,20-DIHYDROXY-21-METHOXY-24-[(2-METHOXY-PHENYL)-THIO]-24-(TRIMETHYLSILYL)-5-BETA-CHOL-23-ENE")
| SpectraBase Compound ID | IiuPU8rZj3k |
|---|---|
| InChI | InChI=1S/C35H56O4SSi/c1-33-19-16-25(36)22-24(33)12-13-26-27-14-15-31(34(27,2)20-17-28(26)33)35(37,23-38-3)21-18-32(41(5,6)7)40-30-11-9-8-10-29(30)39-4/h8-11,18,24-28,31,36-37H,12-17,19-23H2,1-7H3/b32-18+/t24-,25+,26+,27+,28+,31+,33+,34+,35?/m1/s1 |
| InChIKey | FWXLGWMYVZMFSQ-OCHFPXFUSA-N |
| Mol Weight | 601.0 g/mol |
| Molecular Formula | C35H56O4SSi |
| Exact Mass | 600.366858 g/mol |
| Enantiomer InChIKey | FWXLGWMYVZMFSQ-ZICNIWNNSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
t-Butyl 3-.beta.-methoxy-21-.alpha.-hydroxy-21-azido-23-nor-5-.alpha.-cholanoate
4-[3'-.beta.-Methoxy-5'-.alpha.-androstan-17'-yl]-4-hydroxypyrrolidin-2-one
(3S,9S,10S,13R,14S)-17-[2-[(7-chloro-1,2,3,4-tetrahydroacridin-9-yl)amino]ethyl]-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ol
5.beta.-Pregnane-3.alpha.,17.alpha.,20.alpha.-triol, O3,O20-bis-TMS
Acetamide, N-[(3.beta.,5.alpha.)-3-hydroxyfurostan-26-yl]-
5β-pregnane-3α,17,20β-triol, 20-acetate
17.alpha.-Hydroxy-pregnanolone, O,O'-bis-TMS
FWDWUWPIWNWLFQ-RRLFLMLHSA-N
17.alpha.,25-Dihydroxy-5.alpha.-cholestan-3.beta.-yl acetate
| Title | Journal or Book | Year |
|---|---|---|
| A synthesis of 3.beta.-hydroxy-5.beta.,14.alpha.-bufa-20,22-dienolide from deoxycorticosterone | The Journal of Organic Chemistry | 1983 |