(20S)-20-Nitroamino-5a-pregnan-3b-yl acetate
Compound with spectra: 1 NMR
| SpectraBase Compound ID | 5Swqe0NCJPI |
|---|---|
| InChI | InChI=1S/C23H38N2O4/c1-14(24-25(27)28)19-7-8-20-18-6-5-16-13-17(29-15(2)26)9-11-22(16,3)21(18)10-12-23(19,20)4/h14,16-21,24H,5-13H2,1-4H3/t14?,16-,17-,18-,19+,20-,21-,22-,23+/m0/s1 |
| InChIKey | BVULDLHVJFXCFR-NAGUFCJESA-N |
| Mol Weight | 406.6 g/mol |
| Molecular Formula | C23H38N2O4 |
| Exact Mass | 406.283158 g/mol |
| Enantiomer InChIKey | BVULDLHVJFXCFR-CLZBLCTPSA-N |
| Copyright | Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
3.beta.-Acetoxy-5.alpha.-ergost-24(28)-ene
3.beta.-Acetoxy-24-methylene-5.alpha.-cholestane
3.alpha.-Acetoxyandrostane-17-(3-butanoic acid)
METHYL-3-ACETYLLITHOCHOLATE
Methyl (20S)-3.beta.-acetoxy-5.alpha.-cholanate
Lithocholic acid, methyl ester acetate
METHYL-3-ALPHA-ACETOXY-5-BETA-CHOLAN-24-OATE
METHYL-3-BETA-ACETOXY-5-BETA-CHOLAN-24-OATE
24,24,26,26-Tetramethyl-5.alpha.-cholestan-3.beta.-ol - acetate
| Title | Journal or Book | Year |
|---|---|---|
| Steroidal N-nitroamines. Part 4. Intramolecular functionalization of N-nitroamine radicals: synthesis of 1,4-nitroimine compounds | J. Chem. Soc., Perkin Trans. 1 | 1988 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
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