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3β-Acetoxy-6α-chloroergosta-7,22-dien-5α-ol is a complex steroid compound characterized by a cholesterol-like ring system. It features 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 holds significance in the realms of organic chemistry and biochemistry due to its role as a precursor to numerous bioactive molecules and its prospective applications in the pharmaceutical industry. Its distinctive structural attributes and properties render it a compelling subject for chemical synthesis and structural analysis, suggesting potential physiological functions within biological systems.

58261-88-4

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58261-88-4 Usage

Uses

Used in Pharmaceutical Industry:
3β-Acetoxy-6α-chloroergosta-7,22-dien-5α-ol serves as a crucial precursor in the synthesis of various bioactive molecules, making it instrumental in the development of pharmaceuticals. Its unique structural components contribute to its potential use in creating novel therapeutic agents.
Used in Organic Chemistry Research:
As a complex steroid with a distinctive structure, 3β-Acetoxy-6α-chloroergosta-7,22-dien-5α-ol is utilized in organic chemistry research for the exploration of chemical synthesis techniques and the investigation of its reactivity and properties.
Used in Biochemical Studies:
3β-Acetoxy-6α-chloroergosta-7,22-dien-5α-ol is applied in biochemical studies to understand its potential physiological roles and interactions within biological systems, which can provide insights into the development of new bioactive compounds and therapeutic strategies.

Check Digit Verification of cas no

The CAS Registry Mumber 58261-88-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,2,6 and 1 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 58261-88:
(7*5)+(6*8)+(5*2)+(4*6)+(3*1)+(2*8)+(1*8)=144
144 % 10 = 4
So 58261-88-4 is a valid CAS Registry Number.

58261-88-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3β-Acetoxy-6α-chloroergosta-7,22-dien-5α-ol

1.2 Other means of identification

Product number -
Other names 3SS-ACETOXY-6A-CHLOROERGOSTA-7,22-DIEN-5A-OL

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:58261-88-4 SDS

58261-88-4Downstream Products

58261-88-4Relevant academic research and scientific papers

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

-

, (2008/06/13)

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.

Method of inhibiting the hyperproliferation of malignant cells

-

, (2008/06/13)

1α-hydroxy vitamin D4 and analogues, preferably 1,24 dihydroxy vitamin D4, which are useful as active compounds of pharmaceutical compositions for the inhibition of hyperproliferative activity of malignant cells.

Chromyl Halide Oxidation of Steroid Alkenes

Barrett, Anthony G. M.,Barton, Derek H. R.,Tsushima, Tadahiko

, p. 639 - 642 (2007/10/02)

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.

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