1,4,9-Androstatrien-3,17-dione
Compound with spectra: 1 NMR, 1 FTIR, 1 Raman, and 1 MS (GC)
| SpectraBase Compound ID | DM91PK3XOmj |
|---|---|
| InChI | InChI=1S/C19H22O2/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/h7-9,11,14-15H,3-6,10H2,1-2H3/t14-,15-,18-,19-/m0/s1 |
| InChIKey | NNPWVPDIRNJLIN-LNMJFAINSA-N |
| Mol Weight | 282.38 g/mol |
| Molecular Formula | C19H22O2 |
| Exact Mass | 282.16198 g/mol |
| Enantiomer InChIKey | NNPWVPDIRNJLIN-OHDICMOHSA-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 | A4300-000 |
| Copyright | Copyright © 2015-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Sample | Steraloids Inc. |
| Source of Spectrum | Forensic Spectral Research |
| Catalog Number | A4300-000 |
| Copyright | Copyright © 2011-2024 Wiley-VCH GmbH. All Rights Reserved. |
|---|---|
| Source of Spectrum | Prof. Spiteller, University Bayreuth, Germany |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
- Androsta-1,4,9(11)-triene-3,17-dione
- ANDROSTA-1,4,9(11)-TRIEN-3,17-DIONE
- (8S,10S,13S,14S)-10,13-dimethyl-7,8,10,12,13,14,15,16-octahydro-3H-cyclopenta[a]phenanthrene-3,17(6H)-dione
Androsta-4,9(11),16-trien-3-one, 17-methyl-
5.BETA.-ANDROST-9(11)-ENE-3.ALPHA.-OL-17-ONE-TRIMETHYLSILYL ETHER
Androst-9(11)-en-17-one, 3-[(trimethylsilyl)oxy]-, (3.alpha.,5.alpha.)-
9-Dehydrotestosterone
IGTOGZGFKIJBBR-ZBAYIMPASA-N
(3R,4aS,4bS,12aR)-3-Isopropenyl-8-methoxy-12a-methyl-3,4,4a,4b,5,6,12,12a-octahydro-1(2H)-chrysenone
Cholesta-5,17(20),24-trien-3-ol, acetate, (3.beta.)-
(4'R,4'aR,8'aS)-3',4',8'a-trimethyl-4'-(2-triisopropylsilyloxyethyl)spiro[1,3-dioxolane-2,8'-4a,5,6,7-tetrahydronaphthalene]-1'-one
(25R)-3.beta.,26-Bis(tert-butyldimethylsilyloxy)cholest-5-ene-3.beta.,26-diol
3.beta.,26-bis[(t-Butyldimethyl)silyloxy]-cholest-5-ene
| Title | Journal or Book | Year |
|---|---|---|
| Microbial hydroxylation of steroids. 10. Rearrangement during epoxidation and hydroxylation, and the stepwise nature of these enzymic reactions | Canadian Journal of Chemistry | 1985 |
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