5,6-BETA-EPOXY-ESTR-4-ENE-17-BETA-OL-3-ONE
Compound with spectra: 1 NMR
| SpectraBase Compound ID | IEW7CSEgoa2 |
|---|---|
| InChI | InChI=1S/C18H24O3/c1-18-7-6-11-10-3-2-9(19)8-12(10)16-17(21-16)15(11)13(18)4-5-14(18)20/h8,10-11,13-17,20H,2-7H2,1H3 |
| InChIKey | DBWWAGJEOBCAGZ-UHFFFAOYSA-N |
| Mol Weight | 288.39 g/mol |
| Molecular Formula | C18H24O3 |
| Exact Mass | 288.172545 g/mol |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
17-BETA-CYANO-17-ALPHA-HYDROXYANDROST-4-EN-3-ONE
17-Acetoxy-androst-5-ene-7-one
11-ALPHA,13-DIHYDROGLUCOZALUZANIN-C
ent-1.beta.-acetoxy-16-.alpha.-hydroxy-17-noratis-13-ene
ent-1.beta.-acetoxy-16-.beta.-hydroxy-17-noratis-13-ene
6-ALPHA-HYDROXY-B-NORTESTOSTERONE
Estra-3,5-diene-3,6,17.beta.-triol, O,O',O''''-tris-TMS
Pregn-5-en-3-ol, 20-[2-(1-methylethenyl)cyclopropyl]-, (3.beta.,20R)-
BETA-STIGMASTEROL_STEARATE
DELTA(5)-PREGNENE-3-BETA,16-BETA,20(R)-TRIOL-3-O-ACETATE
| 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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