B-Homoandrost-4-ene-2.beta.,7a.beta.,17.beta.-triol-3-one 17-acetate
Compound with spectra: 1 NMR, and 1 MS (GC)
| SpectraBase Compound ID | KZgl9vOgIen |
|---|---|
| InChI | InChI=1S/C22H32O5/c1-12(23)27-19-7-5-14-20-15(8-9-21(14,19)2)22(3)11-18(26)17(25)10-13(22)4-6-16(20)24/h10,14-16,18-20,24,26H,4-9,11H2,1-3H3 |
| InChIKey | WEZPRNODADJDQT-UHFFFAOYSA-N |
| Mol Weight | 376.5 g/mol |
| Molecular Formula | C22H32O5 |
| Exact Mass | 376.224974 g/mol |
| 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 |
Cholest-4-en-3-one, 2-(acetyloxy)-, (2.alpha.)-
Pregn-4-ene-3,20-dione, 2,21-dihydroxy-, (2.alpha.)-
2-BETA,21-DIHYDROXY-4-PREGNEN-3,20-DIONE
Clostebol acetate TMS
2-BETA-HYDROXY-PROGESTERONE
2-Formyl-testosterone-17-formate
7.beta.,25-Dihydroxycholesta-4,23-dien-3-one
17-Acetoxy-androst-5-ene-7-one
17-BETA-ACETYLOXY-ANDROST-5-EN-7-ONE
4,20-Pregnadien-1.beta.-hydroxy-2.beta.-chloro-3-one
| 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:
Wiley Registry of Mass Spectral Data 2023
Author: Wiley
The foundation library for any analytical laboratory running mass spectrometry, the Wiley Registry provides the broadest coverage available in any mass spectral library Learn more.