A-NORANDROST-4-ENE-11-ALPHA,17-BETA-DIOL-3-ONE-17-ACETATE
Compound with spectra: 1 NMR, and 2 MS (GC)
| SpectraBase Compound ID | D6K17ULKkQa |
|---|---|
| InChI | InChI=1S/C20H28O4/c1-11(21)24-17-7-6-15-14-5-4-12-8-13(22)9-19(12,2)18(14)16(23)10-20(15,17)3/h8,14-18,23H,4-7,9-10H2,1-3H3/t14-,15-,16+,17-,18+,19-,20-/m0/s1 |
| InChIKey | KFILSTUXQZJERZ-FLIUJYPFSA-N |
| Mol Weight | 332.44 g/mol |
| Molecular Formula | C20H28O4 |
| Exact Mass | 332.198759 g/mol |
| Enantiomer InChIKey | KFILSTUXQZJERZ-DXXZMKCOSA-N |
| Copyright | Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Spectrum | I-63-1130-0 |
| 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 |
- A-Norandrost-3(5)-en-2-one, 17-(acetyloxy)-11-hydroxy-, (11.alpha.,17.beta.)-
Corticosterone 21-acetate
11 β-hydroxycholest-4-en-3-one
11.beta.,20-Dihydroxy-3-oxopregn-4-en-21-al
11 β, 20 α, 21-trihydroxypregn-4-en-3-one
11β,20β,21-trihydroxypregn-4-en-3-one
11α,20β,21-trihydroxypregn-4-en-3-one
(11-alpha,16-beta)-11,16-dihydroxypregna-4-ene-3-one
(22-E)-11-BETA-HYDROXY-24-NORCHOLESTA-1,4,22-TRIEN-3-ONE
(11-alpha,17E)-11-Hydroxypregna-4,17-diene,3,16-dione
ANDROST-5-ENE-3.BETA.,11.BETA.,17.BETA.-TRIOL(3.BETA.,17.BETA.-DI-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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