Methyldesoxycholate
Compound with spectra: 5 NMR, 2 FTIR, 1 Raman, and 1 MS (GC)
| SpectraBase Compound ID | 9xzzMPQMjwU |
|---|---|
| InChI | InChI=1S/C25H42O4/c1-15(5-10-23(28)29-4)19-8-9-20-18-7-6-16-13-17(26)11-12-24(16,2)21(18)14-22(27)25(19,20)3/h15-22,26-27H,5-14H2,1-4H3/t15-,16-,17-,18+,19-,20+,21+,22+,24+,25-/m1/s1 |
| InChIKey | ZHUOOEGSSFNTNP-JMKDMENQSA-N |
| Mol Weight | 406.6 g/mol |
| Molecular Formula | C25H42O4 |
| Exact Mass | 406.30831 g/mol |
| Enantiomer InChIKey | ZHUOOEGSSFNTNP-CWUYTQBYSA-N |
| Copyright | Copyright © 2012-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Sample | Steraloids Inc. |
| Source of Spectrum | Forensic Spectral Research |
| Catalog Number | C1130-000 |
| Technique | KBr0 |
| Copyright | Copyright © 2014-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Sample | Steraloids Inc. |
| Source of Spectrum | Forensic Spectral Research |
| Catalog Number | C1130-000 |
| Copyright | Copyright © 2009-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
| Copyright | Copyright © 2013-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Sample | Steraloids Inc. |
| Source of Spectrum | Forensic Spectral Research |
| Catalog Number | C1130-000 |
| Copyright | Copyright © 2024 DigiLab GmbH and Wiley-VCH GmbH. All Rights Reserved. |
|---|---|
| Source of Spectrum | DigiLab GmbH (C) 2024 |
| Technique | GC/MS |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CH2Cl2 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | DIOXANE |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
- Deoxycholic acid methyl ester
- 5β-Cholanic acid-3α, 12α-diol methyl ester
- Methyldeoxycholate
- 5b-Cholan-24-oic acid-3a,12a-diol, methyl ester
- METHYL-3-ALPHA,12-ALPHA-DIHYDROXY-5-BETA-CHOLAN-24-OATE
- 3-ALPHA,12-ALPHA-DIHYDROXY-5-BETA-CHOLSAEUREMETHYLESTER
- Desoxycholic acid ME
- methyl 4-((1R,3aS,3bR,5aR,7R,9aS,9bS,11S,11aR)-7,11-dihydroxy-9a,11a-dimethylhexadeca\rhydro-1H-cyclopenta[a]phenanthren-1-yl)pentanoate
DEOXYCHOLIC-ACID;3-ALPHA,12-ALPHA-DIHYDROXY-5-BETA-CHOLAN-24-OIC-ACID
Deoxy-cholic acid, anion
Deoxycholic acid, sodium salt monohydrate
Cholestan-24-one, 3,12-dihydroxy-, (3.alpha.,5.beta.,12.alpha.)-
Glycoallodeoxycholic acid
Glycine, N-[(3.alpha.,5.beta.,12.alpha.)-3,12-dihydroxy-24-oxocholan-24-yl]-
| Title | Journal or Book | Year |
|---|---|---|
| Shortcut Access to Peptidosteroid Conjugates: Building Blocks for Solid-Phase Bile Acid Scaffold Decoration by Convergent Ligation | Molecules | 2011 |
| Carbon-13 NMR spectra of hydroxylated bile acid stereoisomers | Organic Magnetic Resonance | 1983 |
| 13C n.m.r. spectra of steroids —a survey and commentary | Organic Magnetic Resonance | 1977 |
| Nuclear magnetic resonance spectroscopy. Carbon-13 spectra of cholic acids and hydrocarbons included in sodium desoxycholate solutions | Journal of the American Chemical Society | 1973 |
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