6,7-BETA-EPOXY-ANDROST-4-ENE-3,17-DIONE
Compound with spectra: 1 NMR
| SpectraBase Compound ID | LVD5E2ctBiJ |
|---|---|
| InChI | InChI=1S/C19H24O3/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/h9,11-12,15-17H,3-8H2,1-2H3/t11-,12-,15-,16-,17+,18+,19-/m0/s1 |
| InChIKey | VXUAXLOVFFOKOO-FOIWVJDZSA-N |
| Mol Weight | 300.4 g/mol |
| Molecular Formula | C19H24O3 |
| Exact Mass | 300.172545 g/mol |
| Enantiomer InChIKey | VXUAXLOVFFOKOO-AIMBULFCSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
6.beta.,7.beta.Dihydro-1'H-azirino[6,7]androst-4-ene-3,17-dione
6-ALPHA,7-BETA-DIHYDROXY-1,4-ANDROSTADIENE-3,17-DIONE
Androsta-1,4-diene-3,17-dione, 6,7-difluoro-, (6.alpha.,7.alpha.)-
3-BETA-HYDROXY-3-ALPHA-NONAFLUOROBUTYL-ANDROST-5-EN-17-ONE
3,5-Cycloandrostan-17-one, 6-methoxy-, (3.beta.,5.alpha.,6.beta.)-
VERAMILINE-3-GLUCOPYRANOSIDE
Androstan-5α,6α-epoxy-3β-ol-17-one
3'-ALPHA-[BETA-SITOSTERYL-3-BETA-OXY]-DIHYDRONEPETALACTONE
| 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
The KnowItAll NMR Spectral Library offers a comprehensive collection of NMR reference spectra, including NMR, CNMR, and XNMR, and covers a wide range of compounds including organics, polymers, monomers, metabolites, and more. Learn more.