ANDROST-4-ENE-2-BETA,17-BETA-DIOL-3-ONE
Compound with spectra: 2 NMR, and 1 MS (GC)
| SpectraBase Compound ID | 7czQX5b6bie |
|---|---|
| InChI | InChI=1S/C19H28O3/c1-18-8-7-14-12(13(18)5-6-17(18)22)4-3-11-9-15(20)16(21)10-19(11,14)2/h9,12-14,16-17,21-22H,3-8,10H2,1-2H3/t12-,13-,14-,16-,17-,18-,19-/m0/s1 |
| InChIKey | ZOIPFFUVGMVQGE-LXKHFVGGSA-N |
| Mol Weight | 304.43 g/mol |
| Molecular Formula | C19H28O3 |
| Exact Mass | 304.203845 g/mol |
| Enantiomer InChIKey | ZOIPFFUVGMVQGE-REXXFTAASA-N |
| 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 | CHCl3 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CD3OD |
- 2-BETA-HYDROXY-TESTOSTERONE
- (2S,8R,9S,10R,13S,14S,17S)-2,17-dihydroxy-10,13-dimethyl-6,7,8,9,10,11,12,13,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3(2H)-one
- 2,17-DIHYDROXYANDROST-4-EN-3-ONE
(2R,8S,9S,10R,13R,14S,17S)-17-ethyl-2,10,13-trimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one
Testosterone methoxime, 1.Isomer
(3E)-17.beta.-Hydroxyandrost-4-en-3-one - O-[3'-(methoxycarbonyl)propyl]oxime
(3Z)-17.beta.-Hydroxyandrost-4-en-3-one - O-[3'-(methoxycarbonyl)propyl]oxime
(3E)-17.beta.-Hydroxyandrost-4-en-3-one - O-[3'-(hydroxycarbonyl)propyl]oxime
(3Z)-17.beta.-Hydroxyandrost-4-en-3-one - O-[3'-(hydroxycarbonyl)propyl]oxime
(SYN)-17-BETA-HYDROXY-4-ANDROSTEN-3-O-ISOPROPYLOXIME
(ANTI)-17-BETA-HYDROXY-4-ANDROSTEN-3-O-ISOPROPYLOXIME
17-BETA-HYDROXY-3-CYClOETHYLENEDITHIOANDROST-4-ENE
No Name
| Title | Journal or Book | Year |
|---|---|---|
| Structure and stereochemistry of products of hydroxylation of human steroid hormones by a housefly cytochrome P450 (CYP6A1) | Magnetic Resonance in Chemistry | 2006 |
| Microbial hydroxylation of steroids. Part 12. Hydroxylation of testosterone and related steroids by Gnomoniafructicola ATCC 11430 | Canadian Journal of Chemistry | 1989 |
KnowItAll NMR Spectral Library
Author: Wiley
The KnowItAll NMR Spectral Library offers a comprehensive collection of NMR reference spectra, including NMR, CNMR, and XNMR, and covers a wide range of compounds including organics, polymers, monomers, metabolites, and more. Learn more.