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2-Propenoic acid, 2-methyl-3-[4-(1-methylethyl)phenyl]-(9CI), also known as 2-methyl-3-(4-isopropyphenyl)acrylic acid, is a chemical compound with the molecular formula C12H14O2. It is a derivative of acrylic acid, featuring a 2-methyl group and a 4-isopropyphenyl substituent on the 3-position. This organic compound is characterized by its unsaturated carboxylic acid structure, which can participate in various chemical reactions, such as polymerization and esterification. It is an important intermediate in the synthesis of certain pharmaceuticals, agrochemicals, and other specialty chemicals due to its unique structural features and reactivity.

3602-26-4

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3602-26-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3602-26-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,0 and 2 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3602-26:
(6*3)+(5*6)+(4*0)+(3*2)+(2*2)+(1*6)=64
64 % 10 = 4
So 3602-26-4 is a valid CAS Registry Number.

3602-26-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methyl-3-(4-propan-2-ylphenyl)prop-2-enoic acid

1.2 Other means of identification

Product number -
Other names 2-METHYL-3-[4-(ISOPROPYL)PHENYL]-ACRYLIC ACID

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:3602-26-4 SDS

3602-26-4Relevant academic research and scientific papers

Synthesis and SAR study of modulators inhibiting tRXRα-dependent AKT activation

Wang, Zhi-Gang,Chen, Liqun,Chen, Jiebo,Zheng, Jian-Feng,Gao, Weiwei,Zeng, Zhiping,Zhou, Hu,Zhang, Xiao-Kun,Huang, Pei-Qiang,Su, Ying

, p. 632 - 648 (2013/05/09)

RXRα represents an intriguing and unique target for pharmacologic interventions. We recently showed that Sulindac and a designed analog could bind to RXRα and modulate its biological activity, including inhibition of the interaction of an N-terminally truncated RXRα (tRXRα) with the p85α regulatory subunit of phosphatidylinositol-3-OH kinase (PI3K). Here we report the synthesis, testing and SAR of a series of novel analogs of Sulindac as potential modulators for inhibiting tRXRα-dependent AKT activation. A new compound 30 was identified to have improved biological activity.

A facile one-pot conversion of acetates of the Baylis-Hillman adducts to [E]-α-methylcinnamic acids

Basavaiah,Krishnamacharyulu,Hyma,Sarma,Kumaragurubaran

, p. 1197 - 1200 (2007/10/03)

A simple and convenient stereoselective synthesis of [E]-α- methylcinnamic acids via the nucleophilic addition of hydride ion from sodium borohydride to methyl 3-acetoxy-3-aryl-2-methylenepropanoates followed by hydrolysis and crystallization is described

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