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(22e,24s)-de-a,b-8.beta.-(benzoyloxy)-25-[(methoxymethyl)oxy]ergost-22-ene

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

(22e,24s)-de-a,b-8.beta.-(benzoyloxy)-25-[(methoxymethyl)oxy]ergost-22-ene
SpectraBase Compound ID 3CHKLRaNLze
InChI InChI=1S/C28H42O4/c1-20(14-15-21(2)27(3,4)31-19-30-6)23-16-17-24-25(13-10-18-28(23,24)5)32-26(29)22-11-8-7-9-12-22/h7-9,11-12,14-15,20-21,23-25H,10,13,16-19H2,1-6H3/b15-14+/t20-,21-,23-,24?,25+,28-/m1/s1
InChIKey KQMPBBNOXOZNCO-VCTITLDPSA-N
Mol Weight 442.6 g/mol
Molecular Formula C28H42O4
Exact Mass 442.30831 g/mol
Enantiomer InChIKey KQMPBBNOXOZNCO-VXNBZIDHSA-N

View Spectrum of (22e,24s)-de-a,b-8.beta.-(benzoyloxy)-25-[(methoxymethyl)oxy]ergost-22-ene

MS (GC) Spectrum
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Source of Spectrum J-51-1268-11

View Spectrum of (22e,24s)-de-a,b-8.beta.-(benzoyloxy)-25-[(methoxymethyl)oxy]ergost-22-ene

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
(22e,24r)-de-a,b-8.beta.-(benzoyloxy)-25-[(methoxymethyl)oxy]ergost-22-ene
(20R)-Des-A,B-8-benzoyloxy-20-[(p-toluenesulfonyl)-oxymethyl]pregnane
(22-E)-DE-A,B-8-(4-NITROPHENYLSULFENYL)-OXY-24-NORCHOL-22-ENE-23-PHENYLSULFONE
(22-E)-DE-A,B-8-[(TERT.-BUTYLDIMETHYLSILYL)-OXY]-24-NORCHOL-22-ENE-23-PHENYLSULFONE
(22E)-(24R)-Des-A,B-25-(1-methylene-hexyl)-24-[(triethylsilyl)oxy]-26,27-cyclo-22-dehydrocholestane-8.beta.-ol
(8S,20R)-Des-A,B-20-(1',1'-dimethyl-3'-ethoxycarbonyl-allyl)-8.beta.-[(triethylsilyl)oxy]-pregnane
(8S,20R,22R)-Des-A,B-22-cyano-8.beta.,25-bis[(triethylsilyl)oxy]-cholestane
(8S,20R,22.xi.)-Des-A,B-8-[(triethylsilyl)oxy]-22-cyano-25-[(triethylsilyl)oxy]-cholestane
(8S,20S,22.xi.)-Des-A,B-8-[(triethylsilyl)oxy]-22-cyano-25-[(triethylsilyl)oxy]-cholestane
(8S,20S,22S)-Des-A,B-22-cyano-8.beta.,25-bis[(triethylsilyl)oxy]-cholestane
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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