93012-36-3 Usage
General Description
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. However, specific details regarding its properties, uses, or associated hazards are not readily available in the literature and may require additional research to elucidate.
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.
93012-36-3Relevant articles and documents
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.
