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5α-Bromo-6,19-epoxycholestanol 3-Acetate_Molecular_structure_CAS_1258-07-7)
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5α-Bromo-6,19-epoxycholestanol 3-Acetate

Catalog No. B684285 Name Toronto Research Chemicals
CAS Number 1258-07-7 Website http://www.trc-canada.com
M. F. C29H47BrO3 Telephone +1 (416) 665-9696
M. W. 523.58568 Fax +1 (416) 665-4439
Purity Email info@trc-canada.com
Storage Chembase ID: 162883

SYNONYMS

IUPAC name
(1R,2S,5R,6R,9S,10S,12R,13R,15R)-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
IUPAC Traditional name
(1R,2S,5R,6R,9S,10S,12R,13R,15R)-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
Synonyms
(3β,5α,6β)-5-Bromo-6,19-epoxy-cholestan-3-ol Acetate
5α-Bromo-6,19-oxidocholestanol Acetate

DATABASE IDS

CAS Number 1258-07-7

PROPERTIES

Certificate of Analysis Download
Apperance White Solid
Solubility Chloroform
Solubility Cyclohexane
Solubility Dichloromethane
Solubility Ethyl Acetate
Solubility Hexane
MSDS Link Download

DETAILS

Description (English)
Intermediate in the chemical synthesis of cholesterol derivatives, and substrate for producing androsterone derivatives via bacterial steroid biotransformation.

REFERENCES

  • Hadd, H., et al.: Steroids, 31, 453 (1978)
  • Jou, H., et al.: Nuc. Sci. J., 19, 45 (1978)