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5,5'-DiMethyl-[1,1'-biphenyl]-2,2'-dicarboxylic acid is a large, complex chemical compound that belongs to the class of organic compounds known as biphenyls and derivatives. These compounds contain a moiety composed of two phenyl groups linked by a carbon-carbon bond. 5,5'-DiMethyl-[1,1'-biphenyl]-2,2'-dicarboxylic acid contains two carboxylic acid (-COOH) functional groups and two methyl groups on its structure, deriving from phenylacetic acid. Due to its structural features, it could potentially exhibit various biological activities and have different industrial uses.

93012-36-3

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93012-36-3 Usage

Uses

Due to the lack of specific details regarding the properties, uses, or associated hazards of 5,5'-DiMethyl-[1,1'-biphenyl]-2,2'-dicarboxylic acid in the provided materials, it is not possible to list its uses accurately. However, given its structural features, it is likely that 5,5'-DiMethyl-[1,1'-biphenyl]-2,2'-dicarboxylic acid may have potential applications in various industries, such as pharmaceuticals, materials science, or chemical research. Further research and investigation would be required to determine its specific uses and applications.

Check Digit Verification of cas no

The CAS Registry Mumber 93012-36-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,0,1 and 2 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 93012-36:
(7*9)+(6*3)+(5*0)+(4*1)+(3*2)+(2*3)+(1*6)=103
103 % 10 = 3
So 93012-36-3 is a valid CAS Registry Number.

93012-36-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-carboxy-5-methylphenyl)-4-methylbenzoic acid

1.2 Other means of identification

Product number -
Other names 5,5'-dimethyl-diphenic 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:93012-36-3 SDS

93012-36-3Downstream Products

93012-36-3Relevant academic research and scientific papers

Ruthenium(II) Catalysis/Noncovalent Interaction Synergy for Cross-Dehydrogenative Coupling of Arene Carboxylic Acids

Dana, Suman,Chowdhury, Deepan,Mandal, Anup,Chipem, Francis A. S.,Baidya, Mahiuddin

, p. 10173 - 10179 (2018/11/21)

A ruthenium-catalyzed cross-dehydrogenative coupling is developed with the aid of a weakly coordinating carboxylic acid group toward the dimerization of arene carboxylic acids. The protocol is operationally simple and suitable to fabricate diverse homodimerized as well as cross-dimerized products in high yields. Computational insights have also been unveiled to comprehend the plausible reaction mechanism. The critical innovation of the synthetic strategy hinges on the soluble basic additive DBU, which constitutes a synergy of Ru(II)-catalysis with noncovalent interaction and, thus, stabilizes pivotal intermediates to promote the challenging dimerization process.

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