12-BETA-HYDROXY-TESTOSTERONE
Compound with spectra: 2 NMR, and 1 MS (GC)
| SpectraBase Compound ID | 3iEtpEGtBWi |
|---|---|
| InChI | InChI=1S/C19H28O3/c1-18-8-7-12(20)9-11(18)3-4-13-14-5-6-16(21)19(14,2)17(22)10-15(13)18/h9,13-17,21-22H,3-8,10H2,1-2H3/t13-,14-,15-,16-,17+,18-,19-/m0/s1 |
| InChIKey | ALIYDBHAYMSEHU-SLMGBJJTSA-N |
| Mol Weight | 304.43 g/mol |
| Molecular Formula | C19H28O3 |
| Exact Mass | 304.203845 g/mol |
| Enantiomer InChIKey | ALIYDBHAYMSEHU-YOLPFRQPSA-N |
| Copyright | Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Spectrum | F-37-2513-0 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | C5D5N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CD3OD |
- Androst-4-en-3-one, 12,17-dihydroxy-, (12.beta.,17.beta.)-
Androsta-1,4-dien-3-one, 12,17-dihydroxy-, (12.beta.,17.beta.)-
Testosterone, trifluoroacetate
Testosterone, O-TFA
3-OXO-ANDROST-4-ENE-17,3-CARBOXYLIC ACID
3-OXOANDROST-4-ENE-17-CARBOXYLIC ACID
(3'-Oxo-4'-androsten-17.beta.-yl) 3-hydroxy-2-(hydroxymethyl)propionate
4-Androsten-17b-ol-3-one laurate
Undecanoic acid 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 ester
24-nor-Chol-4-ene-22-hydroxy-3-one
20-Hydroxymethyl-pregna-4,20-dien-3-one
| 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 |
| Structure and stereochemistry of products of hydroxylation of human steroid hormones by a housefly cytochrome P450 (CYP6A1) | Magnetic Resonance in Chemistry | 2006 |
KnowItAll NMR Spectral Library
Author: Wiley
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KnowItAll Mass Spectral Library
Author: Wiley
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