606-75-7

Basic information

• Product Name: 3-(2-Carboxyphenyl)benzoic acid
• Synonyms: 3-(2-Carboxyphenyl)benzoic acid
• CAS NO: 606-75-7
• Molecular Formula: C₁₄H₁₀O₄
• Molecular Weight: 242.23
• Mol File: 606-75-7.mol
• Article Data: 1

Chemical Properties

• Melting Point: 215-216 °C(Solv: acetic acid (64-19-7))
• Boiling Point: 471.4±28.0 °C(Predicted)
• Appearance: /
• Density: 1.347±0.06 g/cm3(Predicted)
• PKA: 3.76±0.36(Predicted)
• CAS DataBase Reference: 3-(2-Carboxyphenyl)benzoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(2-Carboxyphenyl)benzoic acid(606-75-7)
• EPA Substance Registry System: 3-(2-Carboxyphenyl)benzoic acid(606-75-7)

Safety Data

• Hazardous Substances Data: 606-75-7(Hazardous Substances Data)

Usage

General Description

3-(2-Carboxyphenyl)benzoic acid is a chemical compound with the molecular formula C14H10O4. It is a white to off-white powder with a molecular weight of 242.23 g/mol. 3-(2-Carboxyphenyl)benzoic acid is a derivative of benzoic acid and contains a carboxy group and a phenyl group. It is commonly used as a starting material in organic synthesis and as a reagent in chemical research. 3-(2-Carboxyphenyl)benzoic acid has also been studied for its potential applications in pharmaceuticals and materials science due to its unique chemical structure and properties.

Upstream product

• 38570-92-2 9-oxo-9H-fluorene-3-carboxylic acid 
• 611-43-8 2,3'-dimethyl-1,1'-biphenyl 
• 932-31-0 ortho-tolylmagnesium bromide 
• 108-42-9 3-chloro-aniline 
• 108-90-7 chlorobenzene 
• 854726-99-1 2'-methyl-5,6-dihydro-[1,1'-bi(phenyl)]-3(4H)-one 
• 1573-92-8 9-oxo-9H-fluorene-1-carboxylic acid 
• 124-38-9 carbon dioxide 
• 25569-80-6 2,3'-dichloro-1,1'-biphenyl 

Downstream Products

• 121-91-5 isophthalic acid 
• 1573-92-8 9-oxo-9H-fluorene-1-carboxylic acid 
• 92-52-4 biphenyl 
• 486-25-9 9-fluorenone 
• 124-38-9 carbon dioxide 

Relevant articles and documents

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

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.