58261-88-4

Basic information

• Product Name: 3β-Acetoxy-6α-chloroergosta-7,22-dien-5α-ol
• Synonyms: 3β-Acetoxy-6α-chloroergosta-7,22-dien-5α-ol;(3β,5α,6α,22E)-6-Chloro-ergosta-7,22-diene-3,5-diol 3-Acetate
• CAS NO: 58261-88-4
• Molecular Formula: C30H47ClO3
• Molecular Weight: 491.14538
• Product Categories: Steroids
• Mol File: 58261-88-4.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• Solubility: Chloroform, Ethyl Acetate
• CAS DataBase Reference: 3β-Acetoxy-6α-chloroergosta-7,22-dien-5α-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 3β-Acetoxy-6α-chloroergosta-7,22-dien-5α-ol(58261-88-4)
• EPA Substance Registry System: 3β-Acetoxy-6α-chloroergosta-7,22-dien-5α-ol(58261-88-4)

Safety Data

• Hazardous Substances Data: 58261-88-4(Hazardous Substances Data)

Usage

General Description

3β-Acetoxy-6α-chloroergosta-7,22-dien-5α-ol is a steroid compound with a complex chemical structure. It consists of a cholesterol-like ring system with an acetoxy group at the 3β position, a chlorine atom at the 6α position, and a hydroxyl group at the 5α position. 3β-Acetoxy-6α-chloroergosta-7,22-dien-5α-ol is important in the field of organic chemistry and biochemistry, as it is a precursor to various bioactive molecules and has potential pharmaceutical applications. Its unique structure and properties make it a valuable target for chemical synthesis and structural analysis, and it may have important physiological roles in biological systems.

Upstream product

• 1108-03-8 ergosterol acetate 
• 75-05-8 acetonitrile 

Relevant articles and documents

Methods of treating skin disorders with novel 1a-hydroxy vitamin D4 compounds and derivatives thereof

The disclosure is of methods of treating various skin disorders, including skin cancer, with compounds of novel 1α-hydroxy vitamin D4 and novel analogues, thereof, including 1,25 dihydroxy vitamin D4 and 1,24 dihydroxy vitamin D4. Novel 1α-hydroxy vitamin D4 compounds and compounds of novel analogues suitable for use in the treatment of such disorders are also disclosed herein.

Chromyl Halide Oxidation of Steroid Alkenes

Ergosteryl acetate and CrO2F2 gave 3β-acetoxy-6α-fluoroergosta-7,22-dien-5α-ol.Cholesteryl acetate and CrO2Cl2 gave the α- and β-epoxides, the 5α-chloro-6-ketone, and both 5α,6β-chlorohydrins; cis-chlorohydrins were not detected.Cholesteryl acetate and CrO2F2 gave both epoxides and the 5α-fluoro-6β-alcohol.Unexpectedly, 9,11-dehydrotigogenin acetate and CrO2F2 gave only the 9,11-epoxides with the β-form predominating (5:1).The absence of cis-halogenohydrin formation from simple olefins and CrO2X2 (X = F, Cl) is in conflict with recent studies on acyclic and monocyclic alkenes.