ANDROSTA-1,4-DIENE-11-ALPHA,17-BETA-DIOL-3-ONE-17-ACETATE
Compound with spectra: 1 NMR, and 1 MS (GC)
| SpectraBase Compound ID | COrhj15dg6U |
|---|---|
| InChI | InChI=1S/C21H28O4/c1-12(22)25-18-7-6-16-15-5-4-13-10-14(23)8-9-20(13,2)19(15)17(24)11-21(16,18)3/h8-10,15-19,24H,4-7,11H2,1-3H3/t15-,16-,17+,18-,19+,20-,21-/m0/s1 |
| InChIKey | UFSKYLAIGDMNQE-FAXLKHNMSA-N |
| Mol Weight | 344.45 g/mol |
| Molecular Formula | C21H28O4 |
| Exact Mass | 344.198759 g/mol |
| Enantiomer InChIKey | UFSKYLAIGDMNQE-VKPOMUGMSA-N |
| Copyright | Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Spectrum | I-63-1130-0 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
- Androsta-1,4-dien-3-one, 17-(acetyloxy)-11-hydroxy-, (11.alpha.,17.beta.)-
(22-E)-11-BETA-HYDROXY-24-NORCHOLESTA-1,4,22-TRIEN-3-ONE
11b,21-Dihydroxy-1,4-pregnadiene-3,20-dione
11b-Hydroxy-1,4-pregnadiene-3,20-dione
(8S,9S,10R,13S,14S,17S)-17-acetyl-11-hydroxy-10,13-dimethyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-3-one
A-NORANDROST-4-ENE-11-ALPHA,17-BETA-DIOL-3-ONE-17-ACETATE
1,4,17(20)-pregnatrien-11β,21-diol-3-one
11-BETA,16-ALPHA-DIHYDROXY-ANDROSTA-1,4-DIENE-3,17-DIONE
Corticosterone 21-acetate
24(.xi.)-methylcholest-5-ene-1.alpha.,3.beta.,11.alpha.-triol
ANDROSTA-1,4-DIENE-11.ALPHA.-OL-3,17-DIONE(11.ALPHA.-TRIMETHYLSILYL ETHER)
| Title | Journal or Book | Year |
|---|---|---|
| Microbial hydroxylation of steroids. 11. Hydroxylation of A-nor-, B-homo-Δ1-, and Δ1-testosterone acetates by Rhizopusarrhizus | Canadian Journal of Chemistry | 1985 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
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KnowItAll Mass Spectral Library
Author: Wiley
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