(22e,24s)-de-a,b-25-[(methoxymethyl)oxy]ergost-22-en-8.beta.-ol
Compound with spectra: 1 NMR
![(22e,24s)-de-a,b-25-[(methoxymethyl)oxy]ergost-22-en-8.beta.-ol](/api/compound/Cp5yYJncZkc.png?ph=true&h=300&w=458 "(22e,24s)-de-a,b-25-[(methoxymethyl)oxy]ergost-22-en-8.beta.-ol")
| SpectraBase Compound ID | Cp5yYJncZkc |
|---|---|
| InChI | InChI=1S/C21H38O3/c1-15(9-10-16(2)20(3,4)24-14-23-6)17-11-12-18-19(22)8-7-13-21(17,18)5/h9-10,15-19,22H,7-8,11-14H2,1-6H3/b10-9+/t15-,16-,17-,18?,19+,21-/m1/s1 |
| InChIKey | LBHSVFGWJHBJHG-NXVGEPQMSA-N |
| Mol Weight | 338.5 g/mol |
| Molecular Formula | C21H38O3 |
| Exact Mass | 338.282095 g/mol |
| Enantiomer InChIKey | LBHSVFGWJHBJHG-PLWSHNTNSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
(8S,20S,22R)-des-A,B-22-methyl-cholestane-8.beta.,25-diol
(8S,20R,22R)-des-A,B-22-methyl-cholestane-8.beta.,25-diol
(8.beta.24S)-De-A,B-cholesta-8,24,25-triol cyclic 24,25-(1-methylethylidene acetal)
DE-A,B-23,24-DI-NOR-22-(PARA-TOLUENESULFONOXY)-CHOLAN-8-BETA-OL;(VITAMIN-D-DERIVATIVE)
(1R,3aR,7aR)-1-[(E,1R,4S)-5-hydroxy-1,4,5-trimethyl-hex-2-enyl]-7a-methyl-2,3,3a,5,6,7-hexahydro-1H-inden-4-one
(8.beta.)-De-A,B-8-Methoxymethyloxy-23,24-dinorcholan-22-ol
(8.beta.)-De-A,B-8-Methoxymethyloxy-24-oxacholestane
(18E)-18-(Hydroxyimino)-des-A,B-cholestan-8-.beta.-ol
Naphtho[2,1-b]furan, dodecahydro-6,9a-dimethyl-, [3aS-(3a.alpha.,5a.alpha.,6.beta.,9a.beta.,9b.alpha.)]-
Naphtho[2,1-b]furan, dodecahydro-6,9a-dimethyl-, [3aR-(3a.alpha.,5a.beta.,6.alpha.,9a.alpha.,9b.beta.)]-
| 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 |