1740-97-2 Usage
General Description
4-isopropyl-m-cresol, also known as IPC, is a synthetic chemical compound commonly used as an antimicrobial agent and a preservative in a variety of products such as personal care products, cosmetics, and pharmaceuticals. It is a white crystalline solid that is insoluble in water and has a faint, pleasant odor. IPC has strong antibacterial and antifungal properties, making it effective in controlling the growth of microorganisms that can spoil or contaminate products. It is often used in combination with other preservatives to provide broad-spectrum protection against a wide range of microorganisms. IPC is generally regarded as safe for use in these applications when used in accordance with regulatory guidelines and at concentrations that do not exceed the maximum allowable limits.
Check Digit Verification of cas no
The CAS Registry Mumber 1740-97-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,4 and 0 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1740-97:
(6*1)+(5*7)+(4*4)+(3*0)+(2*9)+(1*7)=82
82 % 10 = 2
So 1740-97-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H14O/c1-7(2)9-4-5-10(11)8(3)6-9/h4-7,11H,1-3H3
1740-97-2Relevant articles and documents
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Arbuzov,B.A. et al.
, (1965)
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IMPROVEMENTS IN OR RELATING TO ORGANIC COMPOUNDS
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, (2020/01/08)
Disclosed is a compound represented by formula (I). The half-doted double lines each represent a carbon-carbon single bond or a carbon-carbon double bond. The six-membered ring comprises exactly one endocyclic carbon-carbon double bond or exactly two endocyclic carbon-carbon double bonds. When the six-membered ring comprises exactly two endocyclic carbon-carbon double bonds, the endocyclic carbon-carbon double bonds are either in 1,3-relationship or in 1,4-relationship. R is selected from the group consisting of iso-propyl, iso-butyl, sec-butyl and tert-butyl.
Enantioselective Synthesis of (+)-Chamaecypanone C: A Novel Microtubule Inhibitor
Dong, Suwei,Hamel, Ernest,Bai, Ruoli,Covell, David G.,Beutler, John A.,Porco Jr., John A.
supporting information; experimental part, p. 1494 - 1497 (2009/07/25)
A bicycle built for tubulin: The Total synthesis of (+)- chamaecypanone C has been achieved by using a tandem retro-Diels-Alder cascade reaction (see scheme). Initial biological studies demonstrate that (+)- chamaecypanone C is an inhibitor of tubulin assembly and binds at the colchicine site.
