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Methyldesoxycholate
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
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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