B-Homoandrost-4-ene-2.beta.,6.beta.,7a.beta.,17.beta.-tetrol-3-one 17-acetate
Compound with spectra: 1 NMR, and 1 MS (GC)
| SpectraBase Compound ID | DxzSUElQ0rt |
|---|---|
| InChI | InChI=1S/C22H32O6/c1-11(23)28-19-5-4-12-20-13(6-7-21(12,19)2)22(3)10-18(27)16(25)8-14(22)15(24)9-17(20)26/h8,12-13,15,17-20,24,26-27H,4-7,9-10H2,1-3H3 |
| InChIKey | IBCNNNVJDDEARS-UHFFFAOYSA-N |
| Mol Weight | 392.5 g/mol |
| Molecular Formula | C22H32O6 |
| Exact Mass | 392.219889 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 |
4,5-Dehydro-20-nor-stanozolol, N-TMS, O-Acetyl
HELIGENIN-A;(2R,3R,20R)-2,20-DIHYDROXY-3,21-DIMETHOXY-PREGN-5-EN-7-ONE
Clostebol, O,O'-bis-TBS
3,11,20-Trioxopregn-4-en-21-al, 21-(phenylhydrazone)
PIVLINNUXVTTSR-WEEVPDBJSA-N
5-ALPHA,10-BETA,14-BETA-TRIHYDROXY-2-ALPHA-4(20),11-TAXADIENE
6H-3,8a-Ethano-1H-2-benzopyran-6-one, 3,4,4a,5-tetrahydro-7-hydroxy-8-[2-(2-hydroxy-1-methyl-5-oxocyclopent yl)ethyl]-3-methoxy-4,4-dimethyl-, [3S-[3.alpha.,4a.beta.,8(1R*,2R*),8a.alpha.]]-
11-(4'-ACETOXY-5'-EPOXY-3'-ACETOXYMETHYLCYCLO-2'-HEXENONE)-DELTA-(8(12))-DRIMENE
6.beta.-(Acetylthio)-testosterone 17-Acetate
(2R,4S,5S)-5-[(3S,8S,9S,10R,13S,14S,17R)-3-[tert-butyl(diphenyl)silyl]oxy-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]-2-(2,2-dimethylpropyl)-4-hydroxyhexanoic acid ethyl ester
| 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 |
Wiley Registry of Mass Spectral Data 12th Edition
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.