A-NOR-ANDROST-3(5)-ENE-1-BETA,17-BETA-DIOL-2-ONE
Compound with spectra: 1 NMR
| SpectraBase Compound ID | 8RRit8p2r4k |
|---|---|
| InChI | InChI=1S/C18H26O3/c1-17-8-7-13-11(12(17)5-6-15(17)20)4-3-10-9-14(19)16(21)18(10,13)2/h9,11-13,15-16,20-21H,3-8H2,1-2H3/t11-,12-,13-,15-,16+,17-,18-/m0/s1 |
| InChIKey | UYLFHDWRRUPJTQ-WOLXCEEKSA-N |
| Mol Weight | 290.4 g/mol |
| Molecular Formula | C18H26O3 |
| Exact Mass | 290.188195 g/mol |
| Enantiomer InChIKey | UYLFHDWRRUPJTQ-DNRMPTOCSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CHCl3 |
1-ALPHA,17-BETA-DIHYDROXY-2-OXA-ANDROST-4-EN-3-ONE
1-Methyltestosterone
ANDROST-4-ENE-2-BETA,17-BETA-DIOL-3-ONE
2-Formyl-testosterone
(8R,9S,10R,13S,14S,17S)-2-benzyl-17-hydroxy-10,13-dimethyl-1,2,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-3H-cyclopenta[a]phenanthren-3-one
2-Hydroxycholest-4-en-3-one
Deoxycorticosterone, mono-TMS
21-Hydroxypregn-4-ene-3,20-dione, methyl carbonate
3-Keto-4-etiocholenic acid, methyl ester
(+)-(20-S)-20-O-CAPRINOYLPREGN-4-EN-3-ONE
| Title | Journal or Book | Year |
|---|---|---|
| Microbial hydroxylation of steroids. Part 12. Hydroxylation of testosterone and related steroids by Gnomoniafructicola ATCC 11430 | Canadian Journal of Chemistry | 1989 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
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