PREGNA-4,8(9)-DIEN-3,20-DIONE
Compound with spectra: 1 NMR
| SpectraBase Compound ID | ErcU138KQxF |
|---|---|
| InChI | InChI=1S/C21H28O2/c1-13(22)17-6-7-18-16-5-4-14-12-15(23)8-10-20(14,2)19(16)9-11-21(17,18)3/h12,17-18H,4-11H2,1-3H3/t17-,18+,20+,21-/m1/s1 |
| InChIKey | OQRWANLYMLMMNO-YXYSEUPNSA-N |
| Mol Weight | 312.45 g/mol |
| Molecular Formula | C21H28O2 |
| Exact Mass | 312.20893 g/mol |
| Enantiomer InChIKey | OQRWANLYMLMMNO-ZSXPUABSSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
3-BETA-ERGOSTA-5,8-DIEN-3-OL
(3beta)-cholesta-5,8-dien-3-ol
Silane, [[(3.beta.,5.alpha.)-ergosta-8,24(28)-dien-3-yl]oxy]trimethyl-
Methyl 3beta-Formyloxy-5beta-androst-8(14)-en-17beta-carboxylate
Ergosta-8,22-dien-3-ol, (3.beta.,5.alpha.,22E,24S)-
Silane, [[(3.beta.,5.alpha.)-cholest-8(14)-en-3-yl]oxy]trimethyl-
Silane, [[(3.beta.)-ergost-8(14)-en-3-yl]oxy]trimethyl-
5-BETA,24-ALPHA-STIGMASTA-8,22-DIEN-3-ONE
Pregn-8(14)-en-20-one, 3-(acetyloxy)-, (3.beta.,5.beta.)-
3b-Acetoxy-5b-pregn-8(14)-en-20-one
| Title | Journal or Book | Year |
|---|---|---|
| Microbial hydroxylation of steroids. 10. Rearrangement during epoxidation and hydroxylation, and the stepwise nature of these enzymic reactions | Canadian Journal of Chemistry | 1985 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
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