606-75-7 Usage
Uses
Used in Organic Synthesis:
3-(2-Carboxyphenyl)benzoic acid serves as a valuable starting material in organic synthesis, facilitating the creation of a broad range of chemical compounds. Its unique structure allows for versatile reactions, making it a popular choice for chemists working on developing new organic molecules.
Used in Chemical Research:
As a reagent, 3-(2-Carboxyphenyl)benzoic acid is utilized in chemical research to explore its properties and reactions. Its role in understanding various chemical processes and mechanisms is significant, contributing to the advancement of chemical knowledge.
Used in Pharmaceutical Industry:
3-(2-Carboxyphenyl)benzoic acid is studied for its potential applications in the pharmaceutical industry. Its unique chemical structure and properties make it a candidate for the development of new drugs and therapeutic agents, potentially leading to breakthroughs in medicine.
Used in Materials Science:
In the field of materials science, 3-(2-Carboxyphenyl)benzoic acid is investigated for its possible use in creating new materials with specific properties. Its chemical structure lends itself to the development of materials with tailored characteristics for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 606-75-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,0 and 6 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 606-75:
(5*6)+(4*0)+(3*6)+(2*7)+(1*5)=67
67 % 10 = 7
So 606-75-7 is a valid CAS Registry Number.
606-75-7Relevant academic research and scientific papers
Formation of cyclopent[a]indene and acenaphthylene from allyl esters of biphenyl mono- and di-carboxylic acids and from biphenyl dicarboxylic anhydrides on flash vacuum pyrolysis at 1000-1100°C
Bapat, Jayant B.,Brown, Roger F.C.,Bulmer, Glenn H.,Childs, Trevor,Coulston, Karen J.,Eastwood, Frank W.,Taylor, Dennis K.
, p. 1159 - 1182 (2007/10/03)
Flash vacuum pyrolysis at 1000-1100°C of the allyl esters of the three isomeric biphenylcarboxylic acids, of the allyl esters of the 12 biphenyldicarboxylic acids and of the three biphenyldicarboxylic anhydrides gave pyrolysates which were examined by 1H n.m.r. spectroscopy at temperatures below -50°C. In all cases the spectra showed the presence of cyclopent[a]indene and acenaphthylene together with other products. Possible mechanisms for these ring contraction and cyclization processes are discussed and the results of pyrolyses of [2,3-13C2]biphenyl-2,3-dicarboxylic anhydride, and [3,4-13C2]-and (2-2H1)-biphenyl-3,4-dicarboxylic anhydrides are reported.
