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5α-Bromo-6,19-epoxycholestanol 3-Acetate , CAS No.1258-07-7
an intermediate in the chemical synthesis of cholesterol d
Basic Description Synonyms 1258-07-7 | 5alpha-Bromo-6,19-epoxycholestan-3beta-ol acetate | [(1R,2S,5R,6R,9S,10S,12R,13R,15S)-13-bromo-5-methyl-6-[(2R)-6-methylheptan-2-yl]-19-oxapentacyclo[10.5.2.01,13.02,10.05,9]nonadecan-15-yl] acetate | 5?-Bromo-6,19-epoxycholestanol 3-Acetate | SCHEMBL Storage Temp Store at -20°C Shipped In Ice chest + Ice pads Product Description 5α-Bromo-6,19-epoxycholestanol 3-Acetate is an intermediate in the chemical synthesis of cholesterol derivatives, and substrate for producing androsterone derivatives via bacterial steroid biotransformation.
Names and Identifiers IUPAC Name [(1R,2S,5R,6R,9S,10S,12R,13R,15S)-13-bromo-5-methyl-6-[(2R)-6-methylheptan-2-yl]-19-oxapentacyclo[10.5.2.01,13.02,10.05,9]nonadecan-15-yl] acetate INCHI InChI=1S/C29H47BrO3/c1-18(2)7-6-8-19(3)23-9-10-24-22-15-26-29(30)16-21(33-20(4)31)11-14-28(29,17-32-26)25(22)12-13-27(23,24)5/h18-19,21-26H,6-17H2,1-5H3/t19-,21+,22+,23-,24+,25+,26-,27-,28+,29+/m1/s1 InChi Key YEACHZHDRMYMDK-FMSSLCCRSA-N Canonical SMILES CC(C)CCCC(C)C1CCC2C1(CCC3C2CC4C5(C3(CCC(C5)OC(=O)C)CO4)Br)C Isomeric SMILES C[C@H](CCCC(C)C)[C@H]1CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2C[C@@H]4[C@@]5([C@@]3(CC[C@@H](C5)OC(=O)C)CO4)Br)C PubChem CID 102074 Molecular Weight 523.59
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