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(22R,23Z)-DE-A,B-8-BETA-(BENZOYLOXY)-25-[(METHOXYMETHYL)-OXY]-CHOLEST-23-EN-22-OL

Compound with spectra: 2 NMR

(22R,23Z)-DE-A,B-8-BETA-(BENZOYLOXY)-25-[(METHOXYMETHYL)-OXY]-CHOLEST-23-EN-22-OL
SpectraBase Compound ID E32isK3W1iK
InChI InChI=1S/C27H40O5/c1-19(23(28)15-17-26(2,3)31-18-30-5)21-13-14-22-24(12-9-16-27(21,22)4)32-25(29)20-10-7-6-8-11-20/h6-8,10-11,15,17,19,21-24,28H,9,12-14,16,18H2,1-5H3/b17-15-/t19-,21+,22?,23?,24-,27+/m0/s1
InChIKey WMLOBCDEOSZZAO-VMCKWQOISA-N
Mol Weight 444.6 g/mol
Molecular Formula C27H40O5
Exact Mass 444.287574 g/mol
Enantiomer InChIKey WMLOBCDEOSZZAO-SSYKJVJLSA-N

View Spectrum of (22R,23Z)-DE-A,B-8-BETA-(BENZOYLOXY)-25-[(METHOXYMETHYL)-OXY]-CHOLEST-23-EN-22-OL

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3

View Spectrum of (22R,23Z)-DE-A,B-8-BETA-(BENZOYLOXY)-25-[(METHOXYMETHYL)-OXY]-CHOLEST-23-EN-22-OL

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • (22S,23Z)-DE-A,B-8-BETA-(BENZOYLOXY)-25-[(METHOXYMETHYL)-OXY]-CHOLEST-23-EN-22-OL
(22s,23z)-de-a,b-8.beta.-(benzoyloxy)-25-[(methoxymethyl)oxy]chlest-23-en-22-ol
(22S,23E)-8-BETA-(BENZOYLOXY)-25-[(TRIETHYLSILYL)-OXY]-DES-A,B-CHOLEST-23-EN-22-OL
(22s)-de-a,b-8.beta.-(benzoyloxy)-25-[(methoxymethyl)oxy]cholest-23-yn-22-ol
(22R)-DE-A,B-8-BETA-(BENZOYLOXY)-25-[(METHOXYMETHYL)-OXY]-CHOLEST-23-YN-22-OL
(22R,23E)-8-BETA-[(TERT.-BUTYLDIMETHYLSILYL)-OXY]-25-[(METHOXYMETHYL)-OXY]-DES-A,B-CHOLEST-23-EN-22-OL
(22R,23E)-8-BETA-HYDROXY-25-[(METHOXYMETHYL)-OXY]-DES-A,B-CHOLEST-23-EN-22-YL_DIETHYL_PHOSPHATE
(4R)-2-[(1S)-1-[(1R,3aR,4S,7aR)-4-[tert-butyl(dimethyl)silyl]oxy-7a-methyl-1,2,3,3a,4,5,6,7-octahydroinden-1-yl]ethyl]-4-hydroxy-5-methyl-hexanenitrile
(22-R)-DE-A,B-18,22-CYCLO-8-HYDROXY-24-NORCHOLAN-23-PHENYLSULFONE
CALCIFEROL-F
(2S)-[2-(TERT.-BUTYLDIMETHYLSILANOXY)-ETHYL]-(3S)-ISOPROPYL-(1R)-[(2R)-METHOXY-(2R)-PHENYL-3,3,3-TRIFLUOROPROPIONATO]-(2S)-METHYLCYCLOPENTANE
Title Journal or Book Year
Studies on the synthesis of side-chain hydroxylated metabolites of vitamin D. 2. Stereocontrolled synthesis of 25-hydroxyvitamin D2 The Journal of Organic Chemistry 1986
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