4-Pregnen-6β-ol-3, 20-dione
Compound with spectra: 2 NMR, and 2 FTIR
| SpectraBase Compound ID | KVC0zuYpQ46 |
|---|---|
| InChI | InChI=1S/C21H30O3/c1-12(22)15-4-5-16-14-11-19(24)18-10-13(23)6-8-21(18,3)17(14)7-9-20(15,16)2/h10,14-17,19,24H,4-9,11H2,1-3H3/t14-,15+,16-,17-,19+,20+,21+/m0/s1 |
| InChIKey | PWCLWZOSAFOXFL-CXICGXRGSA-N |
| Mol Weight | 330.47 g/mol |
| Molecular Formula | C21H30O3 |
| Exact Mass | 330.219495 g/mol |
| Enantiomer InChIKey | PWCLWZOSAFOXFL-QIDSQCPVSA-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 | Q3210-000 |
| Technique | KBr1 0.65mg |
| Copyright | Copyright © 2012-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Sample | Steraloids |
| Source of Spectrum | Forensic Spectral Research |
| Catalog Number | Q3210-000 |
| 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 |
- 6b-Hydroxyprogesterone
- 6-BETA-HYDROXY-PREGN-4-EN-3,20-DION
6-BETA,21-DIHYDROXYPREGNA-4-EN-3,20-DIONE
6ALPHA-FLUOROPREGN-4-EN-3,20-DIONE
6-Methylpregn-4-ene-3,20-dione
4-Pregnen-6β-bromo-3, 20-dione
6.beta.-Hydroxy-24-ethylcholesta-4,24(28)-dien-3-one
6-BETA,25-DIHYDROXYCHOLESTA-4,23-DIEN-3-ONE
6-BETA-24-EPSILON-DIHYDROXYCHOLESTA-4,25-DIEN-3-ONE
6-.beta.-Hydroxy-,beta.-sitosterone
| Title | Journal or Book | Year |
|---|---|---|
| Predominant allylic hydroxylation at carbons 6 and 7 of 4 and 5-ene functionalized steroids by the thermophilic fungus Rhizomucor tauricus IMI23312 | The Journal of Steroid Biochemistry and Molecular Biology | 2008 |
| 13C n.m.r. spectra of steroids —a survey and commentary | Organic Magnetic Resonance | 1977 |