20β-Hydroxyprogesterone
Compound with spectra: 4 NMR, 4 FTIR, 1 Raman, and 1 UV-Vis
| SpectraBase Compound ID | 6ZcEWiUMqIY |
|---|---|
| InChI | InChI=1S/C21H32O2/c1-13(22)17-6-7-18-16-5-4-14-12-15(23)8-10-20(14,2)19(16)9-11-21(17,18)3/h12-13,16-19,22H,4-11H2,1-3H3/t13-,16+,17-,18+,19+,20+,21-/m1/s1 |
| InChIKey | RWBRUCCWZPSBFC-SJOKZOANSA-N |
| Mol Weight | 316.5 g/mol |
| Molecular Formula | C21H32O2 |
| Exact Mass | 316.24023 g/mol |
| Enantiomer InChIKey | RWBRUCCWZPSBFC-VVCWCJAGSA-N |
| Copyright | Copyright © 2009-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Sample | Steraloids Inc. |
| Source of Spectrum | Forensic Spectral Research |
| Catalog Number | Q3630-000 |
| Copyright | Copyright © 1980, 1981-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Sample | L.W. Lewbart, Crozer-Chester Medical Center, Chester, Pennsylvania |
| Solvent | Chloroform-d; Reference=TMS Spectrometer= Varian CFT-20 |
| 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 © 2009-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
| Copyright | Copyright © 2013-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Sample | Steraloids Inc. |
| Source of Spectrum | Forensic Spectral Research |
| Catalog Number | Q3630-000 |
| Copyright | Copyright © 1980, 1981-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Sample | E. MERCK AG, DARMSTADT, GERMANY |
| Technique | KBr WAFER |
| Copyright | Copyright © 2008-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Sample | Steraloids |
| Source of Spectrum | Forensic Spectral Research |
| Catalog Number | Q3630-000 |
| Technique | KBr1 0.55mg |
| Copyright | Copyright © 2008-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Solvent | Methanol |
| Copyright | Copyright © 1980, 1981-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|
- 20(R)-Hydroxyprogesterone
- 4-Pregnen-20b-ol-3-one
- 20b-Hydroxy-4-pregnen-3-one
- 20b-Hydroxy-pregn-4-en-3-one
- PREGN-4-EN-3-ONE, 20B-HYDROXY-,
20-DEOXO-20-HYDROXYMETHYL-PROGESTERONE
20-Hydroxy-3-oxopregn-4-en-21-al
(25R)-26-hydroxycholest-4-en-3-one
(8S,9S,10R,13R,14S,17R)-10,13-dimethyl-17-[(2R)-6-methyl-7-oxidanyl-heptan-2-yl]-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one
26-Hydroxycholest-4-en-3-one
(25RS)-25-Trimethylsilyloxy-27-nor-4-cholestene-3-one
(25R)-26-(Hydroxy)cholest-4-en-3-one 26-acetate
(6R)-6-[(8S,9S,10R,13R,14S,17R)-10,13-dimethyl-3-oxo-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl]-2-methylheptanoic acid methyl ester
Methyl (2S,6R)-6-((8S,10R,13R,14S,17R)-10,13-dimethyl-3-oxo-2,3,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl)-2-methylheptanoate
24-Trimethylsiloxy-4-cholen-3-one
| Title | Journal or Book | Year |
|---|---|---|
| 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 |