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74996-30-8

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74996-30-8 Usage

General Description

Cholesteryl isoamyl ether is a chemical compound that is derived from cholesterol and isoamyl alcohol. It is mainly used as a chiral resolving agent in chromatography, particularly in the separation of enantiomers. CHOLESTERYL ISOAMYL ETHER is of interest in the pharmaceutical and chemical industries due to its ability to separate and purify different chiral compounds. Cholesteryl isoamyl ether is also used as a solvent in various chemical reactions and as a reagent in organic synthesis. It is a colorless, oily liquid with a faint odor, and it is considered to be relatively stable under normal conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 74996-30-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,9,9 and 6 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 74996-30:
(7*7)+(6*4)+(5*9)+(4*9)+(3*6)+(2*3)+(1*0)=178
178 % 10 = 8
So 74996-30-8 is a valid CAS Registry Number.
InChI:InChI=1/C32H56O/c1-22(2)9-8-10-24(5)28-13-14-29-27-12-11-25-21-26(33-20-17-23(3)4)15-18-31(25,6)30(27)16-19-32(28,29)7/h11,22-24,26-30H,8-10,12-21H2,1-7H3

74996-30-8SDS

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 10,13-dimethyl-3-(3-methylbutoxy)-17-(6-methylheptan-2-yl)-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene

1.2 Other means of identification

Product number -
Other names 3-(3-methylbutoxy)cholest-5-ene

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:74996-30-8 SDS

74996-30-8Downstream Products

74996-30-8Relevant articles and documents

The Synthesis of Cholesteryl Alkyl Ethers

Halperin, G.,Gatt, S.

, p. 39 - 42 (2007/10/02)

Seventeen cholesteryl alkyl ethers were synthesized through alcoholysis of cholesterol p-toluenesulfonate.This method was found superior to the etherification of sodium or potassium cholesterylate with alkyl halides or methanesulfonates, especially for the preparation of long-chain unsaturated alkyl ethers of cholesterol of high specific activity.

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