6-Dehydrotestosterone acetate
Compound with spectra: 2 NMR, 2 FTIR, and 2 MS (GC)
| SpectraBase Compound ID | IFdXergqDNF |
|---|---|
| InChI | InChI=1S/C21H28O3/c1-13(22)24-19-7-6-17-16-5-4-14-12-15(23)8-10-20(14,2)18(16)9-11-21(17,19)3/h4-5,12,16-19H,6-11H2,1-3H3/t16-,17-,18-,19-,20-,21-/m0/s1 |
| InChIKey | PWOYPXRFSUICCT-PXQJOHHUSA-N |
| Mol Weight | 328.45 g/mol |
| Molecular Formula | C21H28O3 |
| Exact Mass | 328.203845 g/mol |
| Enantiomer InChIKey | PWOYPXRFSUICCT-UCGFNCKJSA-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 | A0451-000 |
| Copyright | Copyright © 2008-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Sample | Steraloids |
| Source of Spectrum | Forensic Spectral Research |
| Catalog Number | A0451-000 |
| Technique | KBr1 0.53mg |
| 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 © 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 |
- ANDROSTA-4,6-DIEN-17-BETA-ACETOXY-3-ONE
- 17-BETA-(ACETYLOXY)-ANDROSTA-4,6-DIEN-3-ONE
- 3-OXOANDROSTA-4,6-DIEN-17-YL ACETATE
- 17b-Acetoxy-androsta-4,6-diene-3-one
- ANDROSTA-4,6-DIENE-17.BETA.-OL-3-ONE(17.BETA.-ACETATE)
- (8R,9S,10R,13S,14S,17S)-10,13-dimethyl-3-oxo-2,3,8,9,10,11,12,13,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl acetate
.delta.6-Testosterone Enanthate
ANDROSTA-4,6-DIENE-17.BETA.-OL-3-ONE-TRIMETHYLSILYL ETHER
ANDROSTA-4,6-DIENE-17.BETA.-OL-3-ONE(17.BETA.-TRIMETHYLSILYL ETHER)
20-(R)-HYDROXY-9-BETA-10-ALPHA-PREGNA-4,6-DIENE-3-ONE
20-BETA-HYDROXY-21-ACETYLPREGNA-4,6-DIEN-3-ONE
20-BETA,21-DIHYDROXYPREGNA-4,6-DIEN-3-ONE
No Name
(4R)-2-hydroxy-4-[(8S,9S,10R,13R,14S,17R)-3-keto-10,13-dimethyl-1,2,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl]valeric acid methyl ester
(25R)-26-(Hydroxy)cholest-4,6-dien-3-one 26-acetate
| Title | Journal or Book | Year |
|---|---|---|
| Microbial hydroxylation of steroids. 9. Epoxidation of Δ6-3-ketosteroids by Rhizopusarrhizus ATCC 11145, and the mechanism of the 6β hydroxylase enzyme | Canadian Journal of Chemistry | 1984 |
| 13C n.m.r. spectra of steroids —a survey and commentary | Organic Magnetic Resonance | 1977 |
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