de-a,b-8.beta.-(benzoyloxy)-25-[(methoxymethyl)oxy]-cholest-23-yn-22-one
Compound with spectra: 1 NMR
![de-a,b-8.beta.-(benzoyloxy)-25-[(methoxymethyl)oxy]-cholest-23-yn-22-one](/api/compound/3XX1SvoUbGm.png?ph=true&h=300&w=458 "de-a,b-8.beta.-(benzoyloxy)-25-[(methoxymethyl)oxy]-cholest-23-yn-22-one")
| SpectraBase Compound ID | 3XX1SvoUbGm |
|---|---|
| InChI | InChI=1S/C27H36O5/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/h6-8,10-11,19,21-22,24H,9,12-14,16,18H2,1-5H3/t19-,21+,22?,24-,27+/m0/s1 |
| InChIKey | KHCJJTDZYYBWIM-HVPODGHGSA-N |
| Mol Weight | 440.6 g/mol |
| Molecular Formula | C27H36O5 |
| Exact Mass | 440.256274 g/mol |
| Enantiomer InChIKey | KHCJJTDZYYBWIM-MRDJUJOGSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
(22R)-DE-A,B-8-BETA-(BENZOYLOXY)-25-[(METHOXYMETHYL)-OXY]-CHOLEST-23-YN-22-OL
(22s,23z)-de-a,b-8.beta.-(benzoyloxy)-25-[(methoxymethyl)oxy]chlest-23-en-22-ol
(22R,23Z)-DE-A,B-8-BETA-(BENZOYLOXY)-25-[(METHOXYMETHYL)-OXY]-CHOLEST-23-EN-22-OL
(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
(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
PARALEMNOLIN-P
Labdanolide
(1R,3aS,4S,7aR)-1-[(E,2R)-5,6-dimethylhept-3-en-2-yl]-4-[2-(5-hydroxy-2-methylphenyl)ethyl]-7a-methyl-2,3,3a,4,6,7-hexahydro-1H-inden-5-one
CALICOFEROL-D
| 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 |