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(20R)-18-JODOPREGN-5-ENE-3-BETA,20-DIOL-3-ACETATE

Compound with spectra: 1 NMR, and 1 MS (GC)

(20R)-18-JODOPREGN-5-ENE-3-BETA,20-DIOL-3-ACETATE
SpectraBase Compound ID x3lT78WQJn
InChI InChI=1S/C23H35IO3/c1-14(25)19-6-7-21-18-5-4-16-12-17(27-15(2)26)8-10-22(16,3)20(18)9-11-23(19,21)13-24/h4,14,17-21,25H,5-13H2,1-3H3/t14-,17-,18+,19+,20-,21-,22-,23-/m0/s1
InChIKey SHRXHVQGOCEPEI-PQHDWWGMSA-N
Mol Weight 486.4 g/mol
Molecular Formula C23H35IO3
Exact Mass 486.16309 g/mol
Enantiomer InChIKey SHRXHVQGOCEPEI-KGMQJHTOSA-N

View Spectrum of (20R)-18-JODOPREGN-5-ENE-3-BETA,20-DIOL-3-ACETATE

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum KC-1989-410-22

View Spectrum of (20R)-18-JODOPREGN-5-ENE-3-BETA,20-DIOL-3-ACETATE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • Pregn-5-ene-3,20-diol, 18-iodo-, 3-acetate, (3.beta.,20S)-
(20S)-18-JODOPREGN-5-ENE-3-BETA,20-DIOL-3-ACETATE
(20R)-18-Iodo-pregn-5-ene-3b,20-diol 3-acetate
3-BETA-FORMYLOXY-20-BETA-HYDROXY-18-IODO-PREGN-5-ENE
1H,3H-Naphth[2',1':4,5]indeno[1,7a-c]furan, pregn-5-en-3-ol deriv.
(20R)-3.beta.-Acetoxy-20-hydroxypregn-5-ene
DELTA(5)-PREGNENE-3-BETA,20(R)-DIOL-3-O-MONOACETATE
20(R)-PREGN-5-ENE-3,20-DIOL-3-MONOACETATE
20(S)-PREGN-5-ENE-3,20-DIOL-3-MONOACETATE
3-.beta.-Acetoxy-20-(2-oxo-3-octenyl)pregn-5-ene
20-(FORMYLOXY)PREGN-5-EN-3-YL ACETATE
Title Journal or Book Year
Intramolecular hydrogen abstraction. Hypervalent organoiodine compounds, convenient reagents for alkoxyl radical generation J. Chem. Soc., Perkin Trans. 1 1989

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