(22R,23E)-8-BETA-HYDROXY-25-[(METHOXYMETHYL)-OXY]-DES-A,B-CHOLEST-23-EN-22-YL_DIETHYL_PHOSPHATE
Compound with spectra: 1 NMR
![(22R,23E)-8-BETA-HYDROXY-25-[(METHOXYMETHYL)-OXY]-DES-A,B-CHOLEST-23-EN-22-YL_DIETHYL_PHOSPHATE](/api/compound/LGK0W7Ve01K.png?ph=true&h=300&w=458 "(22R,23E)-8-BETA-HYDROXY-25-[(METHOXYMETHYL)-OXY]-DES-A,B-CHOLEST-23-EN-22-YL_DIETHYL_PHOSPHATE")
| SpectraBase Compound ID | LGK0W7Ve01K |
|---|---|
| InChI | InChI=1S/C24H45O7P/c1-8-29-32(26,30-9-2)31-22(14-16-23(4,5)28-17-27-7)18(3)19-12-13-20-21(25)11-10-15-24(19,20)6/h14,16,18-22,25H,8-13,15,17H2,1-7H3/b16-14+/t18-,19+,20-,21-,22-,24+/m0/s1 |
| InChIKey | QDHDYNDBRLCVDE-MRFJIZGHSA-N |
| Mol Weight | 476.6 g/mol |
| Molecular Formula | C24H45O7P |
| Exact Mass | 476.290291 g/mol |
| Enantiomer InChIKey | QDHDYNDBRLCVDE-KVNCFZHCSA-N |
| Copyright | Copyright © 2016-2025 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,23E)-8-BETA-[(TERT.-BUTYLDIMETHYLSILYL)-OXY]-25-[(METHOXYMETHYL)-OXY]-DES-A,B-CHOLEST-23-EN-22-OL
(8S,20R,22R)-Des-A,B-22-formyl-8.beta.,25-bis[(triethylsilyl)oxy]-cholestane
(8S,20R,22S)-Des-A,B-22-formyl-8.beta.,25-bis[(triethylsilyl)oxy]-cholestane
(8S,20R,22.xi.)-Des-A,B-8-[(triethylsilyl)oxy]-22-formyl-25-[(triethylsilyl)oxy]-cholestane
(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
(8S,20S,22.xi.)-Des-A,B-8-[(triethylsilyl)oxy]-22-cyano-25-[(triethylsilyl)oxy]-cholestane
(8S,20S,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
| Title | Journal or Book | Year |
|---|---|---|
| A Short, Efficient Copper-Mediated Synthesis of 1α,25-Dihydroxyvitamin D2 (1α,25-Dihydroxyergocalciferol) and C-24 Analogs1,2 | The Journal of Organic Chemistry | 1997 |