4,6-Androstadien-3,17-dione
Compound with spectra: 2 NMR, 1 FTIR, 1 Raman, and 2 MS (GC)
| SpectraBase Compound ID | 9wjFtqSQkDB |
|---|---|
| InChI | InChI=1S/C19H24O2/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/h3-4,11,14-16H,5-10H2,1-2H3/t14-,15-,16-,18-,19-/m0/s1 |
| InChIKey | YEWSFUFGMDJFFG-QAGGRKNESA-N |
| Mol Weight | 284.4 g/mol |
| Molecular Formula | C19H24O2 |
| Exact Mass | 284.17763 g/mol |
| Enantiomer InChIKey | YEWSFUFGMDJFFG-BQUOXIOCSA-N |
| Copyright | Copyright © 2014-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Sample | Steraloids Inc. |
| Source of Spectrum | Forensic Spectral Research |
| Catalog Number | A0420-000 |
| Copyright | Copyright © 2013-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Sample | Steraloids Inc. |
| Source of Spectrum | Forensic Spectral Research |
| Catalog Number | A0420-000 |
| Copyright | Copyright © 2011-2024 Wiley-VCH GmbH. All Rights Reserved. |
|---|---|
| Source of Spectrum | Dr. Makin, London Hospital Medical College, UK |
| Copyright | Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Spectrum | RCM-23-217-6 |
| 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 |
- 6-Dehydroandrostenedione
- ANDROST-4,6-DIEN-3,17-DIONE
- Androsta-4,6-diene-3,17-dione
- (8R,9S,10R,13S,14S)-10,13-dimethyl-9,10,11,12,13,14,15,16-octahydro-1H-cyclopenta[a]phenanthrene-3,17(2H,8H)-dione
4,6-Pregnadien-3-one
3,5-Androstadien-3-ol-17-one 3-ethyl ether
3-BETA-HYDROXY-B-NORANDROST-5-ENE-17-ONE
5-ALPHA-ANDROST-6-ENE-3,17-DIONE
6-Androstene-3,17-dione
5-BETA-ANDROST-6-ENE-3,17-DIONE
Androst-4-ene-3,17-dione, 18-hydroxy-
Androst-4-ene-3,17-dione, 19-bromo-
Androst-5-en-17-one, 3-[(diethylsilyl)oxy]-, (3.beta.)-
Androst-4-ene-3,17-dione, 19-iodo-
| 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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