5a-Cholestan-3a-ol
Compound with spectra: 6 NMR, 1 FTIR, and 1 MS (GC)
| SpectraBase Compound ID | FKrE895x2ug |
|---|---|
| InChI | InChI=1S/C27H48O/c1-18(2)7-6-8-19(3)23-11-12-24-22-10-9-20-17-21(28)13-15-26(20,4)25(22)14-16-27(23,24)5/h18-25,28H,6-17H2,1-5H3/t19-,20+,21-,22+,23-,24+,25+,26+,27-/m1/s1 |
| InChIKey | QYIXCDOBOSTCEI-FBVYSKEZSA-N |
| Mol Weight | 388.7 g/mol |
| Molecular Formula | C27H48O |
| Exact Mass | 388.370516 g/mol |
| Enantiomer InChIKey | QYIXCDOBOSTCEI-NQVBFBCSSA-N |
| Copyright | Copyright © 2009-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
| Copyright | Copyright © 1980, 1981-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Sample | M. L. LEWBART, CROZER-CHESTER MEDICAL CENTER, CHESTER, PENNSYLVANIA |
| Technique | 4000-1350 CM^-^1=MULLED IN PERFLUORINATED HYDROCARBON; 1350-450 CM^-^1=MULLED IN MINERAL OIL |
| 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 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | PYRIDINE-D5 |
| 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 |
- 3-ALPHA-CHOLESTANOL
- EPICHOLESTANOL
- CHOLESTAN-3-OL
- 3.ALPHA.-HYDROXY-5.ALPHA.-CHOLESTAN
- (3R,5S,8R,9S,10S,13R,14S,17R)-10,13-dimethyl-17-((R)-6-methylheptan-2-yl)hexadecahydro-1H-cyclopenta[a]phenanthren-3-ol
5.alpha.-Cholestan-3.beta.,26-diol
27-nor-5.alpha.-Cholestan-3.beta.-ol
(3R,5R)-10,13-Dimethyl-17-(1-methyl-4-methylsulfanyl-butyl)-hexadecahydro-cyclopenta[a]phenanthren-3-ol
5-(3-Hydroxy-10,13-dimethyl-hexadecahydro-cyclopenta[a]phenanthren-17-yl)-hexanoic acid methyl ester
Cholestane-3,25-diol, (3.alpha.,5.beta.)-
(3S,5S,8R,9S,10S,13R,14S,17R)-10,13-dimethyl-17-[(2R)-5-methylhexan-2-yl]-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ol
Cholan-3-ol
| Title | Journal or Book | Year |
|---|---|---|
| Terpenoids and sterols from the wood of Abies pinsapo | Phytochemistry | 1993 |
| Determination of the absolute configuration of a secondary hydroxy group in a chiral secondary alcohol using glycosidation shifts in carbon-13 nuclear magnetic resonance spectroscopy | Journal of the American Chemical Society | 1978 |
| 13C n.m.r. spectra of steroids —a survey and commentary | Organic Magnetic Resonance | 1977 |
| Carbon-13 nuclear magnetic resonance spectra of hydroxy steroids | The Journal of Organic Chemistry | 1976 |