5-ALPHA-ANDROSTANE-2-BETA,3-ALPHA,16-ALPHA,17-BETA-TETROL
Compound with spectra: 1 NMR, and 1 MS (GC)
| SpectraBase Compound ID | 3ZyOUGT2FAF |
|---|---|
| InChI | InChI=1S/C19H32O4/c1-18-6-5-12-11(13(18)8-15(21)17(18)23)4-3-10-7-14(20)16(22)9-19(10,12)2/h10-17,20-23H,3-9H2,1-2H3/t10-,11+,12-,13-,14-,15+,16-,17-,18-,19-/m0/s1 |
| InChIKey | CLNSSHHJJYZUKV-GZIKCXOQSA-N |
| Mol Weight | 324.5 g/mol |
| Molecular Formula | C19H32O4 |
| Exact Mass | 324.23006 g/mol |
| Enantiomer InChIKey | CLNSSHHJJYZUKV-KXTXZCONSA-N |
| Copyright | Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Spectrum | I-67-273-38 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | DMSO-D6 |
- Androstane-2,3,16,17-tetrol, (2.beta.,3.alpha.,5.alpha.,16.alpha.,17.beta.)-
MELIAVOSIN
2-HYDROXYCHOLESTAN-3-YL ACETATE
Cholestane-3,16-diol
2b-Acetamido-3a-cholestanol
Cholestane-2-ethanol, 3-hydroxy-, (2.alpha.,3.beta.,5.alpha.)-
Cholestane-2-ethanol, 3-hydroxy-, (2.alpha.,3.alpha.,5.alpha.)-
5.alpha.-Cholestane-2.alpha.-methanol, 3.beta.-hydroxy-
No Name
16-ALPHA,17-ALPHA-EPOXY-5-ALPHA-ANDROSTANE-3-BETA-OL
1H-Cyclopenta[7,8]phenanthro[2,3-b]furan, cholest-2-eno[3,2-b]furan deriv.
| 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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KnowItAll Mass Spectral Library
Author: Wiley
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