(6-R)-[6-(2)H]-3-BETA-[(BROMOMERCURIO)-METHYL]-5-(HYDROXYMETHYL)-A,B-BISNOR-5-BETA-CHOLESTANE
Compound with spectra: 1 NMR
![(6-R)-[6-(2)H]-3-BETA-[(BROMOMERCURIO)-METHYL]-5-(HYDROXYMETHYL)-A,B-BISNOR-5-BETA-CHOLESTANE](/api/compound/LNsGOp8zATO.png?ph=true&h=300&w=458 "(6-R)-[6-(2)H]-3-BETA-[(BROMOMERCURIO)-METHYL]-5-(HYDROXYMETHYL)-A,B-BISNOR-5-BETA-CHOLESTANE")
| SpectraBase Compound ID | LNsGOp8zATO |
|---|---|
| InChI | InChI=1S/C27H47O.BrH.Hg/c1-18(2)8-7-9-19(3)22-10-11-23-21-16-27(17-28)20(4)12-15-26(27,6)24(21)13-14-25(22,23)5;;/h18-24,28H,4,7-17H2,1-3,5-6H3;1H;/q;;+1/p-1/t19-,20+,21+,22-,23+,24+,25-,26-,27+;;/m1../s1/i17D;;/t17-,19-,20+,21+,22-,23+,24+,25-,26-,27+;; |
| InChIKey | LKNMLMGVIZQBAG-QRFSRMEESA-M |
| Mol Weight | 669.2 g/mol |
| Molecular Formula | C27H462HBrHgO |
| Exact Mass | 669.25795 g/mol |
| Parent InChIKey | DIWMWNHIGFZIKR-KYORHFQZSA-M |
| Enantiomer InChIKey | LKNMLMGVIZQBAG-DQPRDKOWSA-M |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CD2Cl2 |
3-BETA-((BROMOMERCURIO)-METHYL)-A,B-DINOR-5-BETA-CHOLESTANE-5-CARBALDEHYDE
3-BETA-[(BROMOMERCURIO)-METHYL]-A,B-BISNOR-5-BETA-CHOLESTANE-5-CARBALDEHYDE
B-NOR-4-BETA,5-BETA-METHANO-CHOLESTAN-3-ONE
(24Z)-STIGMAST-24(28)-ENE-3-BETA,5-ALPHA,6-BETA-TRIOL
5-VINYL-A,B-BISNOR-5-BETA-CHOLESTANE-3-BETA-CARBALDEHYDE
25-XI-CHOLESTANE-3-BETA,5-ALPHA,6-BETA,26-TETRAOL-26-ACETATE
25.psi.-Cholestane-3.beta.,5.alpha.,6.beta.,26-tetrol - 26-Acetate
CHLOESTANE-3-BETA,5-ALPHA,6-BETA,26-TETROL-26-ACETATE
Cholestane-3.beta.,5.alpha.,6.beta.,26-tetrol - 26-Acetate
25-ZETA-CHOLESTANE-3-BETA,5-ALPHA,6-BETA-26-TETROL-26-ACETATE
| Title | Journal or Book | Year |
|---|---|---|
| An Approach toward the Triquinane-Type Skeleton via Reagent-Controlled Skeletal Rearrangements. A Facile Method for Protection−Deprotection of Organomercurials, Tuning the Selectivity of Wagner−Meerwein Migrations, and a New Route to Annulated Lactones | The Journal of Organic Chemistry | 1998 |