The chemical substance known as (3beta,5alpha,6alpha,10alpha)-5-bromo-6,19-epoxycholestan-3-yl acetate, with the CAS number 1258-07-7, is a steroid derivative characterized by its complex structure, which includes a bromine atom and an epoxide group. This compound is a modified form of cholesterol, featuring a bromine substitution at the 5-position and an epoxide at the 6,19-positions, which can influence its biological activity and reactivity. The presence of the acetate group at the 3-position suggests that it may exhibit ester-like properties, potentially affecting its solubility and interaction with biological membranes. Steroids like this one often play significant roles in biological systems, including hormone regulation and cell membrane structure. The specific stereochemistry indicated by the nomenclature suggests that it has multiple chiral centers, which can contribute to its pharmacological properties. Overall, this compound is of interest in medicinal chemistry and biochemistry for its potential applications and effects on biological systems.

(3beta,5alpha,6alpha,10alpha)-5-bromo-6,19-epoxycholestan-3-yl acetate

1258-07-7: The chemical substance known as (3beta,5alpha,6alpha,10alpha)-5-bromo-6,19-epoxycholestan-3-yl acetate, with the CAS number 1258-07-7, is a steroid derivative characterized by its complex structure, which includes a bromine atom and an epoxide group. This compound is a modified form of cholesterol, featuring a bromine substitution at the 5-position and an epoxide at the 6,19-positions, which can influence its biological activity and reactivity. The presence of the acetate group at the 3-position suggests that it may exhibit ester-like properties, potentially affecting its solubility and interaction with biological membranes. Steroids like this one often play significant roles in biological systems, including hormone regulation and cell membrane structure. The specific stereochemistry indicated by the nomenclature suggests that it has multiple chiral centers, which can contribute to its pharmacological properties. Overall, this compound is of interest in medicinal chemistry and biochemistry for its potential applications and effects on biological systems.

<p>Applications Intermediate in the chemical synthesis of cholesterol derivatives, and substrate for producing androsterone derivatives via bacterial steroid biotransformation.<br>References Hadd, H., et al.: Steroids, 31, 453 (1978), Jou, H., et al.: Nuc. Sci. J., 19, 45 (1982),<br></p>

CAS 1258-07-7

(3beta,5alpha,6alpha,10alpha)-5-bromo-6,19-epoxycholestan-3-yl acetate

5Alpha-Bromo-6,19-epoxycholestanol 3-Acetate

Ref: TR-B684285