2-(4-Chlorophenyl)butanedioic acid, also known as chlorophenylbutanedioic acid, is an organic compound characterized by its structure, which features a butanedioic acid backbone substituted with a 4-chlorophenyl group. This compound typically appears as a white to off-white crystalline solid. It is soluble in polar solvents such as water and methanol, while being less soluble in non-polar solvents. The presence of the chlorophenyl group contributes to its potential biological activity and may influence its reactivity and interaction with other chemical species. The compound can participate in various chemical reactions, including esterification and amidation, making it useful in synthetic organic chemistry. Additionally, its structural features may allow it to act as a ligand in coordination chemistry or as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Safety data should be consulted for handling and exposure guidelines, as with any chemical substance.

2-(4-chlorophenyl)butanedioic acid

58755-91-2: 2-(4-Chlorophenyl)succinic acid, Butanedioic Acid, 2-(4-Chlorophenyl)-

2-(4-Chlorophenyl)succinic acid is a chiral compound that can be used in the enantioseparation of baclofen. It is an enantiopure and enantiomerically pure compound that has shown to have an optimized catalytic activity and yields. 2-(4-Chlorophenyl)succinic acid is a ligand that binds to the enzyme butanoic acid oxidoreductase, which converts butanoic acid into butyric acid. This reaction has been optimized in order to increase the yield of this product by using a catalyst that is more efficient at converting the substrate into product.

CAS 58755-91-2: 2-(4-chlorophenyl)butanedioic acid

2-(4-Chlorophenyl)succinic acid

Ref: 3D-FC51436

2-(4-CHLORO-PHENYL)-SUCCINIC ACID

Ref: IN-DA00E9Q4

2-(4-Chlorophenyl)succinic acid

Ref: 10-F333907