(22R)-DE-A,B-8-BETA-(BENZOYLOXY)-25-[(METHOXYMETHYL)-OXY]-CHOLEST-23-YN-22-OL
Compound with spectra: 1 NMR
![(22R)-DE-A,B-8-BETA-(BENZOYLOXY)-25-[(METHOXYMETHYL)-OXY]-CHOLEST-23-YN-22-OL](/api/compound/9s8LMqkPWTP.png?ph=true&h=300&w=458 "(22R)-DE-A,B-8-BETA-(BENZOYLOXY)-25-[(METHOXYMETHYL)-OXY]-CHOLEST-23-YN-22-OL")
| SpectraBase Compound ID | 9s8LMqkPWTP |
|---|---|
| InChI | InChI=1S/C27H38O5/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/h6-8,10-11,19,21-24,28H,9,12-14,16,18H2,1-5H3/t19-,21+,22?,23-,24-,27+/m0/s1 |
| InChIKey | KZCGXVQSDRGSNX-PAXLJCAHSA-N |
| Mol Weight | 442.6 g/mol |
| Molecular Formula | C27H38O5 |
| Exact Mass | 442.271924 g/mol |
| Enantiomer InChIKey | KZCGXVQSDRGSNX-IMFCCPDWSA-N |
| 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]chlest-23-en-22-ol
(22R,23Z)-DE-A,B-8-BETA-(BENZOYLOXY)-25-[(METHOXYMETHYL)-OXY]-CHOLEST-23-EN-22-OL
(22S,23E)-8-BETA-(BENZOYLOXY)-25-[(TRIETHYLSILYL)-OXY]-DES-A,B-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-HYDROXY-25-[(METHOXYMETHYL)-OXY]-DES-A,B-CHOLEST-23-EN-22-YL_DIETHYL_PHOSPHATE
CALCIFEROL-F
(22-R)-DE-A,B-18,22-CYCLO-8-HYDROXY-24-NORCHOLAN-23-PHENYLSULFONE
(2S)-[2-(TERT.-BUTYLDIMETHYLSILANOXY)-ETHYL]-(3S)-ISOPROPYL-(1R)-[(2R)-METHOXY-(2R)-PHENYL-3,3,3-TRIFLUOROPROPIONATO]-(2S)-METHYLCYCLOPENTANE
5-BETA-HYDROXYMETHYL-10-BETA-ESTRANE-3-BETA,17-BETA-DIOL
| 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 |