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4-Pregnen-6β-ol-3, 20-dione
SpectraBase Compound ID KVC0zuYpQ46
InChI InChI=1S/C21H30O3/c1-12(22)15-4-5-16-14-11-19(24)18-10-13(23)6-8-21(18,3)17(14)7-9-20(15,16)2/h10,14-17,19,24H,4-9,11H2,1-3H3/t14-,15+,16-,17-,19+,20+,21+/m0/s1
InChIKey PWCLWZOSAFOXFL-CXICGXRGSA-N
Mol Weight 330.47 g/mol
Molecular Formula C21H30O3
Exact Mass 330.219495 g/mol
Enantiomer InChIKey PWCLWZOSAFOXFL-QIDSQCPVSA-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 Q3210-000
Technique KBr1 0.65mg
Copyright Copyright © 2012-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Steraloids
Source of Spectrum Forensic Spectral Research
Catalog Number Q3210-000
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CHCl3
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • 6b-Hydroxyprogesterone
  • 6-BETA-HYDROXY-PREGN-4-EN-3,20-DION
Title Journal or Book Year
Predominant allylic hydroxylation at carbons 6 and 7 of 4 and 5-ene functionalized steroids by the thermophilic fungus Rhizomucor tauricus IMI23312 The Journal of Steroid Biochemistry and Molecular Biology 2008
13C n.m.r. spectra of steroids —a survey and commentary Organic Magnetic Resonance 1977
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