A-NORANDROST-4-ENE-17-BETA-OL-3-ONE-ACETATE
Compound with spectra: 1 NMR, and 1 MS (GC)
| SpectraBase Compound ID | 9JIaPYMHVps |
|---|---|
| InChI | InChI=1S/C20H28O3/c1-12(21)23-18-7-6-16-15-5-4-13-10-14(22)11-20(13,3)17(15)8-9-19(16,18)2/h10,15-18H,4-9,11H2,1-3H3/t15-,16-,17-,18-,19-,20-/m0/s1 |
| InChIKey | KTVDMDPBIWRLOT-RABCQHRBSA-N |
| Mol Weight | 316.44 g/mol |
| Molecular Formula | C20H28O3 |
| Exact Mass | 316.203845 g/mol |
| Enantiomer InChIKey | KTVDMDPBIWRLOT-BZIXAJQCSA-N |
| Copyright | Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Spectrum | J-60-8214-4 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
- 17.beta.-Hydroxy-4-norandrost-3-en-2-one Acetate
4-Androsten-17b-ol-3-one laurate
(3'-Oxo-4'-androsten-17.beta.-yl) 3-hydroxy-2-(hydroxymethyl)propionate
Testosterone hexenate
Testosterone, O-TFA
Testosterone, trifluoroacetate
1-Glyceryl 3-(3'-oxo-4'-androsten-17.beta.-oxycarbonyl)-propionate
3-OXOANDROST-4-EN-17-YL FORMATE
Testosterone 17-formate
Androst-4-en-17-ol-3-one acetate
17.beta.-Acetoxy-4-androsten-3-ol
| Title | Journal or Book | Year |
|---|---|---|
| Microbial hydroxylation of steroids. 11. Hydroxylation of A-nor-, B-homo-Δ1-, and Δ1-testosterone acetates by Rhizopusarrhizus | Canadian Journal of Chemistry | 1985 |
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