16,(5α)-Androsten-3β-ol
Compound with spectra: 2 NMR, 1 FTIR, 1 Raman, and 2 MS (GC)
| SpectraBase Compound ID | JdXKT7q0ykJ |
|---|---|
| InChI | InChI=1S/C19H30O/c1-18-9-3-4-16(18)15-6-5-13-12-14(20)7-11-19(13,2)17(15)8-10-18/h3,9,13-17,20H,4-8,10-12H2,1-2H3/t13-,14-,15-,16-,17-,18-,19-/m0/s1 |
| InChIKey | KRVXMNNRSSQZJP-LOVVWNRFSA-N |
| Mol Weight | 274.45 g/mol |
| Molecular Formula | C19H30O |
| Exact Mass | 274.229666 g/mol |
| Enantiomer InChIKey | KRVXMNNRSSQZJP-ZLJUKNTDSA-N |
| Copyright | Copyright © 2012-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Sample | Steraloids Inc. |
| Source of Spectrum | Forensic Spectral Research |
| Catalog Number | A9200-000 |
| Copyright | Copyright © 2012-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Sample | Steraloids Inc. |
| Source of Spectrum | Forensic Spectral Research |
| Catalog Number | A9200-000 |
| Copyright | Copyright © 2011-2024 Wiley-VCH GmbH. All Rights Reserved. |
|---|---|
| Source of Spectrum | Dr. Makin, London Hospital Medical College, UK |
| Copyright | Copyright © 2011-2024 Wiley-VCH GmbH. All Rights Reserved. |
|---|---|
| Source of Spectrum | Prof. Spiteller, University Bayreuth, Germany |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
- Epiocclesterol
- 3b-Hydroxy-5a,16-androstene
- DELTA-(16)-3-BETA-ANDROSTENOL
- 5alpha-Androst-16-en-3alpha-ol
- 3.BETA.-HYDROXY-5.ALPHA.-ANDROST-16-ENE
- 5.ALPHA.-ANDROST-16-ENE-3.BETA.-OL
- (3S,5S,8R,9S,10S,13R,14S)-10,13-dimethyl-2,3,4,5,6,7,8,9,10,11,12,13,14,15-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ol
- ANDROST-16-EN-3-OL
3-.alpha.-Fluoro-androst-16-ene
5.beta.-androst-16-en-3-one
Pregnan-3-ol, 20-methyl-, (3.beta.,5.alpha.)-
D-Homo-androstane-3b,17ab-diol
(3-BETA,17A-BETA)-DIHYDROXY-D-HOMOANDROSTAN
1H-Phenanthro[2,1-c]pyran, D-homo-17-oxaandrostane deriv.
3-ANDROSTAN-3-YLANDROSTANE
3-(10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl)-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthrene
3B-TRIMETHYLSILOXY-5A-ANDROSTANE
| Title | Journal or Book | Year |
|---|---|---|
| Transformation of a series of saturated isomeric steroidal diols by Aspergillus tamarii KITA reveals a precise stereochemical requirement for entrance into the lactonization pathway | The Journal of Steroid Biochemistry and Molecular Biology | 2010 |
| Carbon-13 nuclear magnetic resonance spectra of monounsaturated steroids. Evaluation of rules for predicting their chemical shifts | The Journal of Organic Chemistry | 1981 |