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5,16-Pregnadien-3β-ol-20-one acetate, 20-oxime

Compound with spectra: 1 NMR, 2 FTIR, and 1 Raman

5,16-Pregnadien-3β-ol-20-one acetate, 20-oxime
SpectraBase Compound ID GBZkF8PIrIL
InChI InChI=1S/C23H33NO3/c1-14(24-26)19-7-8-20-18-6-5-16-13-17(27-15(2)25)9-11-22(16,3)21(18)10-12-23(19,20)4/h5,7,17-18,20-21,26H,6,8-13H2,1-4H3/t17-,18-,20-,21-,22-,23+/m0/s1
InChIKey OVKSHCIVDWZSJD-RFOVXIPZSA-N
Mol Weight 371.5 g/mol
Molecular Formula C23H33NO3
Exact Mass 371.246044 g/mol
Enantiomer InChIKey OVKSHCIVDWZSJD-ZOGCLFRTSA-N

View Spectrum of 5,16-Pregnadien-3β-ol-20-one acetate, 20-oxime

ATR-IR Spectrum
Copyright Copyright © 2009-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Steraloids Inc.
Source of Spectrum Forensic Spectral Research
Catalog Number P1510-000

View Spectrum of 5,16-Pregnadien-3β-ol-20-one acetate, 20-oxime

1H NMR Spectrum
Copyright Copyright © 2009-2024 John Wiley & Sons, Inc. All Rights Reserved.
Solvent CDCl3

View Spectrum of 5,16-Pregnadien-3β-ol-20-one acetate, 20-oxime

Raman Spectrum
Copyright Copyright © 2013-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Steraloids Inc.
Source of Spectrum Forensic Spectral Research
Catalog Number P1510-000

View Spectrum of 5,16-Pregnadien-3β-ol-20-one acetate, 20-oxime

FTIR Spectrum
Copyright Copyright © 2008-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Steraloids
Source of Spectrum Forensic Spectral Research
Catalog Number P1510-000
Technique KBr1 0.70mg
  • 3b-Hydroxy-5,16-pregnadien-20-one acetate oxime
Pregna-5,16-dien-20-one, 3-[(trimethylsilyl)oxy]-, O-(phenylmethyl)oxime, (3.beta.)-
16-Dehydropregnenolone propionate
Pregna-5,16-dien-20-one, 3,21-bis(acetyloxy)-, (3.beta.)-
5,16-Androstadien-3b-ol-17-carboxylic acid 3-acetate
5,16-Androstadien-3β-ol-17β-carboxylic acid 3-acetate
20-(Acetyloxy)pregna-5,16,20-trien-3-yl acetate
Monotrimethylsilyl 3.beta.,hydroxy-pregn-5,16-diene-20-one
(3.beta.,25S)-26-(Dimethylamino)cholesta-5,16,20(22)-trien-3-ol
3-Acetoxy-17-[1'-(t-butyldimethylsilyloxy)ethenyl]-( C16 unsaturated) - steroid structure
3-hydroxy-20-oxopregna-5,16-dien-21-yl acetate
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