(22R,23E)-25-[(METHOXYMETHYL)-OXY]-8-OXO-DES-A,B-CHOLEST-23-EN-22-YL_DIETHYL_PHOSPHATE
Compound with spectra: 1 NMR
![(22R,23E)-25-[(METHOXYMETHYL)-OXY]-8-OXO-DES-A,B-CHOLEST-23-EN-22-YL_DIETHYL_PHOSPHATE](/api/compound/G0ZRb4w9lED.png?ph=true&h=300&w=458 "(22R,23E)-25-[(METHOXYMETHYL)-OXY]-8-OXO-DES-A,B-CHOLEST-23-EN-22-YL_DIETHYL_PHOSPHATE")
| SpectraBase Compound ID | G0ZRb4w9lED |
|---|---|
| InChI | InChI=1S/C24H43O7P/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/h14,16,18-20,22H,8-13,15,17H2,1-7H3/b16-14+/t18-,19+,20-,22-,24+/m0/s1 |
| InChIKey | XUAPQKKVMLQCNF-XKTDFMRPSA-N |
| Mol Weight | 474.6 g/mol |
| Molecular Formula | C24H43O7P |
| Exact Mass | 474.274641 g/mol |
| Enantiomer InChIKey | XUAPQKKVMLQCNF-GBYJHTTBSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
(22R)-22-Methyl-1.alpha.,25-dihydroxyvitamin D3
(20S,22R)-22-Methyl-1.alpha.,25-dihydroxyvitamin D3
(22S)-22-Methyl-1.alpha.,25-dihydroxyvitamin D3
(20S,22S)-22-Methyl-1.alpha.,25-dihydroxyvitamin D3
(22R,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
(1R,2R,4E,6R)-4-[(2E)-2-[(1R,7aR)-1-[(1R)-5-hydroxy-1,5-dimethyl-hexyl]-7a-methyl-2,3,3a,5,6,7-hexahydro-1H-inden-4-ylidene]ethylidene]-6-(4-hydroxybutoxy)-1-methyl-cyclohexane-1,2-diol
1.alpha.-(4-Hydroxybutoxy)-2.beta.,25-dihydroxy-2.alpha.-methyl-19-norvitamin D3
9,10-Secocholesta-5,7,10(19)-trien-6,19,19-D3-3-ol, (3.beta.,5E,7E)-
(1R,2R,4E,6R)-4-[(2E)-2-[(1R,7aR)-1-[(1R)-5-hydroxy-1,5-dimethyl-hexyl]-7a-methyl-2,3,3a,5,6,7-hexahydro-1H-inden-4-ylidene]ethylidene]-6-(3-hydroxypropoxy)-1-methyl-cyclohexane-1,2-diol
| 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 |