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20,22-[(1-R)-4-HYDROXYBUTYLIDENE]-20-HYDROXYECDYZONE;(20-R,22-R)-20,22-O-[(1-R)-4-HYDROXYBUTYLIDENE]-2-BETA,3-BETA,14-ALPHA,25-TETRAHYDROXY-5-BET

Compound with spectra: 1 NMR

20,22-[(1-R)-4-HYDROXYBUTYLIDENE]-20-HYDROXYECDYZONE;(20-R,22-R)-20,22-O-[(1-R)-4-HYDROXYBUTYLIDENE]-2-BETA,3-BETA,14-ALPHA,25-TETRAHYDROXY-5-BET
SpectraBase Compound ID CrBoei2SSaM
InChI InChI=1S/C31H50O8/c1-27(2,36)11-10-25-30(5,39-26(38-25)7-6-14-32)24-9-13-31(37)19-15-21(33)20-16-22(34)23(35)17-28(20,3)18(19)8-12-29(24,31)4/h15,18,20,22-26,32,34-37H,6-14,16-17H2,1-5H3/t18-,20-,22+,23-,24-,25+,26+,28+,29+,30+,31+/m0/s1
InChIKey ZWWQXUIRDTZMIO-HXALOHLKSA-N
Mol Weight 550.7 g/mol
Molecular Formula C31H50O8
Exact Mass 550.350569 g/mol
Enantiomer InChIKey ZWWQXUIRDTZMIO-XEVQCYHWSA-N

View Spectrum of 20,22-[(1-R)-4-HYDROXYBUTYLIDENE]-20-HYDROXYECDYZONE;(20-R,22-R)-20,22-O-[(1-R)-4-HYDROXYBUTYLIDENE]-2-BETA,3-BETA,14-ALPHA,25-TETRAHYDROXY-5-BET

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CD3OD
Title Journal or Book Year
New Derivatives of 20-Hydroxyecdyzone. Viticosterone E Synthesis Russian Journal of Organic Chemistry 2004
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