6,7-ALPHA-EPOXY-5-BETA-ANDROSTAN-3,17-DIONE
Compound with spectra: 1 NMR
| SpectraBase Compound ID | K5hT1Mopitb |
|---|---|
| InChI | InChI=1S/C19H26O3/c1-18-7-5-10(20)9-13(18)16-17(22-16)15-11-3-4-14(21)19(11,2)8-6-12(15)18/h11-13,15-17H,3-9H2,1-2H3/t11-,12-,13-,15-,16+,17-,18+,19-/m0/s1 |
| InChIKey | BLECRVGLXRQZPL-IUZULKJOSA-N |
| Mol Weight | 302.41 g/mol |
| Molecular Formula | C19H26O3 |
| Exact Mass | 302.188195 g/mol |
| Enantiomer InChIKey | BLECRVGLXRQZPL-DGBPOTMESA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
17.beta.-acetoxy-5.beta.,6.beta.-epoxyandrosten-3-one-3-ethylene Ketal
6,7-BETA-EPOXY-ANDROST-4-ENE-3,17-DIONE
(22S,23S)-2ALPHA,3ALPHA;22,23-DIEPOXY-5ALPHA-ERGOSTAN-6-ONE
Androst-4-ene-3,17-dione, 1,2-epoxy-, (1.beta.,2.beta.)-
(22R,23S,24R)-3.beta.-Acetoxy-22-bromo-23,24-epoxy-24-methyl-5.alpha.-cholestan-6-one
2-BETA-CYANO-1-ALPHA-HYDROXY-4,6-ANDROSTADIENE-3,17-DIONE
N,O-DIACETYL-DIHYDRO-25-ISOVERAZINE-A=(22S,25R)-22,26-ACETYL-EPIMINO-CHOLEST-5-EN-3-BETA-YL-ACETATE
Cholest-5-en-22-yne-20,25-diol, 3-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-, (3.beta.)-
(20R)-26,27-Dipropyl-3.beta.,20,25-trihydroxy-cholest-5-en-22-one
| Title | Journal or Book | Year |
|---|---|---|
| Microbial hydroxylation of steroids. 9. Epoxidation of Δ6-3-ketosteroids by Rhizopusarrhizus ATCC 11145, and the mechanism of the 6β hydroxylase enzyme | Canadian Journal of Chemistry | 1984 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
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