| Identification |
| Name: | Cholestan-3-ol,5-bromo-6,19-epoxy-, acetate, (3b,5a,6b)- (9CI) |
| Synonyms: | 5a-Cholestan-3b-ol, 5-bromo-6b,19-epoxy-, acetate (7CI,8CI);6,10-(Epoxymethano)-10H-cyclopenta[a]phenanthrene, cholestan-3-ol deriv.; 5a-Bromo-6,19-epoxycholestanolacetate; 5a-Bromo-6,19-oxidocholestanolacetate |
| CAS: | 1258-07-7 |
| Molecular Formula: | C29H47 Br O3 |
| Molecular Weight: | 523.5857 |
| InChI: | InChI=1/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 |
| Molecular Structure: |
![(C29H47BrO3) 5a-Cholestan-3b-ol, 5-bromo-6b,19-epoxy-, acetate (7CI,8CI);6,10-(Epoxymethano)-10H-cyclopenta[a]phe...](https://img1.guidechem.com/chem/e/dict/88/1258-07-7.jpg) |
| Properties |
| Flash Point: | 284.5°C |
| Boiling Point: | 546.7°Cat760mmHg |
| Density: | 1.19g/cm3 |
| Refractive index: | 1.54 |
| Flash Point: | 284.5°C |
| Usage: | Intermediate in the chemical synthesis of cholesterol derivatives, and substrate for producing androsterone derivatives via bacterial steroid biotransformation. |
| Safety Data |
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