5-BETA-ANDROST-6-ENE-3,17-DIONE
Compound with spectra: 1 NMR
| SpectraBase Compound ID | 3RpySqBvVqE |
|---|---|
| InChI | InChI=1S/C19H26O2/c1-18-9-7-13(20)11-12(18)3-4-14-15-5-6-17(21)19(15,2)10-8-16(14)18/h3-4,12,14-16H,5-11H2,1-2H3/t12-,14+,15+,16+,18+,19+/m1/s1 |
| InChIKey | BTAPTIJZCKGMRD-QJISAEMRSA-N |
| Mol Weight | 286.42 g/mol |
| Molecular Formula | C19H26O2 |
| Exact Mass | 286.19328 g/mol |
| Enantiomer InChIKey | BTAPTIJZCKGMRD-ZPVXQFEESA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
24-Methyl-3-oxo-5.beta.-chol-6-enoate
5.ALPHA.-ANDROST-6-ENE-17.BETA.-OL-3-ONE(17.BETA.-TRIMETHYLSILYL ETHER)
5.ALPHA.-ANDROST-6-ENE-17.BETA.-OL-3-ONE-TRIMETHYLSILYL ETHER
6-Cholesten-3b-ol
DELTA-(6)-3-BETA-CHOLESTENOL
5-ALPHA-ANDROSTAN-3,7,17-TRIKETONE
Acetonitrile, (1,1-dimethylethoxy)[(5.alpha.)-17-oxoandrostan-3-ylidene]-
6-Cholestene
| 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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