CAS 1258-35-1

5-Bromo-5α-cholestane-3,6-diol 3-Acetate

Description:

5-Bromo-5α-cholestane-3,6-diol 3-Acetate, with the CAS number 1258-35-1, is a steroid derivative characterized by its bromine substitution and acetylation. This compound features a cholestane backbone, which is a saturated steroid structure, and contains hydroxyl groups at the 3 and 6 positions, contributing to its reactivity and potential biological activity. The presence of the bromine atom at the 5 position enhances its lipophilicity and may influence its interaction with biological membranes. The acetylation of the hydroxyl group at the 3 position improves its stability and solubility, making it more amenable for various chemical reactions and applications. Typically, such compounds are of interest in medicinal chemistry and biochemistry due to their potential roles in hormone synthesis, signaling pathways, and as intermediates in the synthesis of more complex steroid derivatives. The specific stereochemistry and functional groups present in 5-Bromo-5α-cholestane-3,6-diol 3-Acetate are crucial for its biological activity and pharmacological properties.

Formula: C₂₉H₄₉BrO₃

Synonyms:

• 3β-Acetoxy-5-broMo-5α-cholestan-6β-ol
• Cholestane-3,6-diol, 5-bromo-, 3-acetate, (3β,5α,6β)-
• 5-Bromo-5α-cholestane-3,6-diol 3-Acetate

5-Bromo-5α-cholestane-3,6-diol 3-Acetate

Controlled Product

CAS: 1258-35-1

Applications Intermediate in the production of cholesterol derivatives.
References Kobayashi, Y., et al.: Chem. Pharm. Bull., 23, 196 (1975), Momose, D., et al.: Chem. Pharm. Bull., 32, 1840 (1984),

Formula: C₂₉H₄₉BrO₃

Color and Shape: White To Off-White

Molecular weight: 525.6

Ref: TR-B682415

5-Bromo-5a-cholestane-3,6-diol 3-acetate

CAS: 1258-35-1

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Formula: C₂₉H₄₉BrO₃

Purity: Min. 95%

Molecular weight: 525.6 g/mol

Ref: 3D-FB19159