11-BETA-FLUOROPREGN-4-ENE-3,20-DIONE
Compound with spectra: 1 NMR
| SpectraBase Compound ID | 9o43tznu5cr |
|---|---|
| InChI | InChI=1S/C21H29FO2/c1-12(23)16-6-7-17-15-5-4-13-10-14(24)8-9-20(13,2)19(15)18(22)11-21(16,17)3/h10,15-19H,4-9,11H2,1-3H3/t15-,16+,17-,18-,19+,20-,21+/m0/s1 |
| InChIKey | XKJYWTJLSGCAQL-ATWVFEABSA-N |
| Mol Weight | 332.46 g/mol |
| Molecular Formula | C21H29FO2 |
| Exact Mass | 332.215158 g/mol |
| Enantiomer InChIKey | XKJYWTJLSGCAQL-WQNFENHCSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
Corticosterone 21-acetate
11β,20α-dihydroxy-3-oxopregn-4-en-21-oic acid, methyl ester
11 β-hydroxycholest-4-en-3-one
11.beta.,20-Dihydroxy-3-oxopregn-4-en-21-al
11α,20β,21-trihydroxypregn-4-en-3-one
11β,20β,21-trihydroxypregn-4-en-3-one
11 β, 20 α, 21-trihydroxypregn-4-en-3-one
11b-Hydroxy-1,4-pregnadiene-3,20-dione
(8S,9S,10R,13S,14S,17S)-17-acetyl-11-hydroxy-10,13-dimethyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-3-one
3,11,20-Trioxopregn-4-en-21-al, 21-(phenylhydrazone)
| Title | Journal or Book | Year |
|---|---|---|
| Microbial hydroxylation of steroids. 8. Incubation of Cn halo- and other substituted steroids with Cn hydroxylating fungi | Canadian Journal of Chemistry | 1982 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
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