5β-Androstan-17β-ol-3-one
Compound with spectra: 3 NMR, 1 FTIR, 1 Raman, and 4 MS (GC)
| SpectraBase Compound ID | DcaOJxyzNgh |
|---|---|
| InChI | InChI=1S/C19H30O2/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/h12,14-17,21H,3-11H2,1-2H3/t12-,14+,15+,16+,17+,18+,19+/m1/s1 |
| InChIKey | NVKAWKQGWWIWPM-MISPCMORSA-N |
| Mol Weight | 290.45 g/mol |
| Molecular Formula | C19H30O2 |
| Exact Mass | 290.22458 g/mol |
| Enantiomer InChIKey | NVKAWKQGWWIWPM-VSTKQYMISA-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 | A3730-000 |
| Copyright | Copyright © 2012-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Sample | Steraloids Inc. |
| Source of Spectrum | Forensic Spectral Research |
| Catalog Number | A3730-000 |
| Copyright | Copyright © 2011-2024 Wiley-VCH GmbH. All Rights Reserved. |
|---|---|
| Source of Spectrum | Prof. Spiteller, University Bayreuth, Germany |
| 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. D. Henneberg, MPI f. Kohlenforschung, Muelheim a.d.R., Germany |
| Copyright | Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Spectrum | KC-1991-1828-14 |
| 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 | CHCl3 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
- 5β-Dihydrotestosterone
- Etiocholan-17β-ol-3-one
- 17β-Hydroxyetiocholan-3-one
- (5-BETA,17-BETA)-17-HYDROXY-3-ANDROSTANONE
- 17b-Hydroxy-5b-androstan-3-one
- (5beta,17beta)-17-hydroxyandrostan-3-one
- 17-Hydroxyandrostan-3-one
- ANDROSTAN-3-ONE, 17-HYDROXY-, (5beta,17beta)-
- (5R,8R,9S,10S,13S,14S,17S)-17-hydroxy-10,13-dimethyltetradecahydro-1H-cyclopenta[a]phenanthren-3(2H)-one
- (1S,2S,7R,10R,11S,14S,15S)-14-hydroxy-2,15-dimethyltetracyclo[8.7.0.0(2,7).0(11,15)]heptadecan-5-one
17.beta.-methyl-5a-androstan-3-one
17.beta.-Fluoroandrostan-3-one
Androstan-3-one, 17-iodo-, (17.alpha.)-
5.alpha.-Pregnan-3-one, oxime
(3-BETA,17A-BETA)-DIHYDROXY-D-HOMOANDROSTAN
3,16-DIKETO-D-HOMOANDROSTAN
(2-BETA,17A-BETA)-DIHYDROXY-D-HOMOANDROSTAN
A-Nor-2,3-secocholestane-2,3-diol, (5.beta.)-
26,27-Dinor-5.beta.-cholestan-24-one
Androstan-3-one, (aminocarbonyl)hydrazone, (5.alpha.)-
| Title | Journal or Book | Year |
|---|---|---|
| Properties of the zinc-nickel chloride-deuterium oxide system: a simple method for deuterium addition to carbon-carbon and carbon-oxygen double bonds | The Journal of Organic Chemistry | 1990 |
| 13C nuclear magnetic resonance spectra of bridged-ring steroids and related compounds | Magnetic Resonance in Chemistry | 1985 |
| 13C n.m.r. spectra of steroids —a survey and commentary | Organic Magnetic Resonance | 1977 |