6809-72-9

Usage

Molecular structure

2-[2-(phenylcarbamoyl)phenyl]benzoic acid contains a benzene ring with two phenylcarbamoyl groups attached to a central benzoic acid molecule.

Use as a chelator

BAPTA is commonly used in biochemical and cellular research as a chelator of calcium ions due to its ability to bind to and sequester these ions.

Applications in studying physiological and pathological processes

BAPTA has been shown to be useful in studying various physiological and pathological processes that involve calcium signaling in cells, such as muscle contraction, neurotransmitter release, and gene expression.

Use in the development of calcium ion-selective electrodes

BAPTA is used in the development of calcium ion-selective electrodes.

Upstream product

• 6050-13-1 biphenyl-2,2'-dicarboxylic acid anhydride 
• 62-53-3 aniline 

Downstream Products

• 27022-16-8 1-phenyl-1H-azepine-2,7-dione 
• 39950-13-5 9-phenyl-9H-pyrano[2,3,4,5-lmn]phenanthridine-5,10-dione 
• 83329-99-1 Biphenyl-2,2'-dicarboxylic acid 2-[(1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazol-4-yl)-amide] 2'-phenylamide 

Relevant academic research and scientific papers

Catalyst-controlled site-selective asymmetric epoxidation of nerylamine and geranylamine derivatives

Novel catalysts for site- and enantioselective epoxidation of nerylamine and geranylamine derivatives have been developed. Although mCPBA oxidation took place selectively at the more electron-rich double bond to give the 6,7-epoxides, these catalysts provide the 2,3-epoxides in moderate to high enantioselectivity via the oxidation of the relatively electron-deficient double bond.

Hypolipidemic activity of N-substituted diphenimides in rodents

A number of N-substituted diphenimide derivatives were investigated for hypolipidemic activity in mice at 20 mg/kg/day I.P. A number of the compounds were found to be more active than clofibrate and equally as active as other cyclic imides reported previously in the literature. N-(4-Methylphenyl)-diphenimide demonstrated the most potent acitivity lowering serum cholesterol levels by 48% and serum triglyceride levels by 40% after 16 days administration of drug.