(22S,23E)-8-BETA-(BENZOYLOXY)-25-[(TRIETHYLSILYL)-OXY]-DES-A,B-CHOLEST-23-EN-22-OL
Compound with spectra: 1 NMR
![(22S,23E)-8-BETA-(BENZOYLOXY)-25-[(TRIETHYLSILYL)-OXY]-DES-A,B-CHOLEST-23-EN-22-OL](/api/compound/I42plm7AWHW.png?ph=true&h=300&w=458 "(22S,23E)-8-BETA-(BENZOYLOXY)-25-[(TRIETHYLSILYL)-OXY]-DES-A,B-CHOLEST-23-EN-22-OL")
| SpectraBase Compound ID | I42plm7AWHW |
|---|---|
| InChI | InChI=1S/C31H50O4Si/c1-8-36(9-2,10-3)35-30(5,6)22-20-27(32)23(4)25-18-19-26-28(17-14-21-31(25,26)7)34-29(33)24-15-12-11-13-16-24/h11-13,15-16,20,22-23,25-28,32H,8-10,14,17-19,21H2,1-7H3/b22-20+/t23-,25+,26-,27-,28-,31+/m0/s1 |
| InChIKey | RXWAUABKHZPBHF-GDDHVRGMSA-N |
| Mol Weight | 514.8 g/mol |
| Molecular Formula | C31H50O4Si |
| Exact Mass | 514.347837 g/mol |
| Enantiomer InChIKey | RXWAUABKHZPBHF-KYTGHMDESA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
(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
(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
(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
19-nor-5,10-seco-Androst-1(10)-ene-3.beta.,5.alpha.,17.beta.-triol - triacetate
(22-R)-DE-A,B-18,22-CYCLO-8-HYDROXY-24-NORCHOLAN-23-PHENYLSULFONE
2-Pentenoic acid, 5-[6-(acetyloxy)decahydro-5,5,8a-trimethyl-2-methylene-1-naphthalenyl]-3-methyl-, [1S-(1.alpha.,4a.beta.,6.alpha.,8a.alpha.)]-
3-ACETOXY-8(20),13-DIENE-15-OIC ACID
| 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 |