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19243-30-2

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19243-30-2 Usage

General Description

22-Ketocholesterol, also known as (3β)-stigmast-5-en-3-ol-22-one, is a biomolecule that belongs to the class of Triterpenoids. It is considered an intermediate in the biosynthesis of steroidal hormones and is particularly involved in the bioconversion of cholesterol into other steroidal hormones. Its structure is closely related to that of cholesterol, but with a ketone functional group at the 22nd carbon atom. Despite this close structural resemblance, 22-ketocholesterol interacts differently with organisms compared to cholesterol. Just like other sterols, this compound plays a crucial role in various biological functions such as membrane fluidity and permeability.

Check Digit Verification of cas no

The CAS Registry Mumber 19243-30-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,2,4 and 3 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 19243-30:
(7*1)+(6*9)+(5*2)+(4*4)+(3*3)+(2*3)+(1*0)=102
102 % 10 = 2
So 19243-30-2 is a valid CAS Registry Number.
InChI:InChI=1/C12H10S3/c13-9-1-5-11(6-2-9)15-12-7-3-10(14)4-8-12/h1-8,13-14H

19243-30-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 22-KETOCHOLESTEROL

1.2 Other means of identification

Product number -
Other names 22-oxocholesterol

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:19243-30-2 SDS

19243-30-2Relevant articles and documents

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Burstein,S. et al.

, p. 13 - 60 (1970)

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Reassignment of configuration to the 22-hydroxycholesterols. Synthesis of (22S)- and (22R)-3H-cholesterols.

Burrows,Hornby,Caspi

, p. 103 - 107 (2007/10/17)

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