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102491-96-3

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102491-96-3 Usage

General Description

(24S)-Ethylcholesta-3,5,22-triene is a chemical compound that belongs to the class of organic compounds known as C27-steroids. It is a sterol derivative, which is a type of lipid molecule that is important for maintaining the structure and function of cell membranes. (24S)-ETHYLCHOLESTA-3,5,22-TRIENE is a cholesterol derivative that plays a crucial role in the body, as it is involved in processes such as hormone production, vitamin D synthesis, and bile acid formation. Its structure consists of a four carbon aliphatic side chain, a double bond at the 5,6-position, and a 3-hydroxy group. Overall, (24S)-ethylcholesta-3,5,22-triene is an important molecule with various biological functions in the human body.

Check Digit Verification of cas no

The CAS Registry Mumber 102491-96-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,4,9 and 1 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 102491-96:
(8*1)+(7*0)+(6*2)+(5*4)+(4*9)+(3*1)+(2*9)+(1*6)=103
103 % 10 = 3
So 102491-96-3 is a valid CAS Registry Number.

102491-96-3SDS

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 (24S)-ETHYLCHOLESTA-3,5,22-TRIENE

1.2 Other means of identification

Product number -
Other names stigmasta-3,5,22t-triene

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:102491-96-3 SDS

102491-96-3Downstream Products

102491-96-3Relevant articles and documents

Convenient synthesis of monomeric steroids from steroidal oxalate dimers using flash vacuum pyrolysis (FVP)

Nahar, Lutfun,Turner, Alan B.,Sarker, Satyajit D.

, p. 359 - 366 (2010)

Flash vacuum pyrolysis (FVP) or thermolysis (FVT), an environmentally friendly method for studying organic reaction mechanisms as well as synthesis, was applied to a series of oxalate dimers (1, 3, 5, 7, 9, 11, 13, and 15) to synthesise monomeric enes, dienes, and a triene (2, 4, 6, 8, 10, 12, 14, and 16). All steroidal monomers were identified by spectroscopic means. TUBITAK.

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