4-Nitrophenylsuccinic acid is an organic compound characterized by its structure, which includes a succinic acid backbone substituted with a nitrophenyl group. This compound typically appears as a crystalline solid and is known for its solubility in polar solvents such as water and alcohols, while being less soluble in non-polar solvents. The presence of the nitro group (-NO2) on the phenyl ring imparts significant polarity and can influence the compound's reactivity, making it a useful intermediate in organic synthesis and pharmaceutical applications. The carboxylic acid functional groups (-COOH) contribute to its acidic properties, allowing it to participate in various chemical reactions, including esterification and amidation. Additionally, 4-nitrophenylsuccinic acid can serve as a potential ligand in coordination chemistry due to its ability to form complexes with metal ions. Its applications extend to biochemical research, where it may be utilized in enzyme assays or as a substrate in various biochemical pathways. Overall, this compound is valued for its versatility in both synthetic and analytical chemistry.

4-Nitrophenylsuccinic acid

21021-53-4: 2-(4-Nitrophenyl)Butanedioic Acid, (2R)-2-(4-nitrophenyl)butanedioate, (2S)-2-(4-nitrophenyl)butanedioate

2-(4-NITROPHENYL)SUCCINIC ACID

4-Nitrophenylsuccinic acid is a hydrocarbon that is a precursor in the formation of phenyl succinic acid during the Friedel-Crafts reaction. The phenyl group is introduced by condensations with aromatic compounds, such as benzene, to form an aromatic hydrocarbon. 4-Nitrophenylsuccinic acid is also used to produce phenylalanine and vitamin B6.

CAS 21021-53-4: 4-Nitrophenylsuccinic acid

2-(4-NITROPHENYL)SUCCINIC ACID

Ref: 10-F333962

4-Nitrophenylsuccinic acid

Ref: 3D-FN51026

2-(4-Nitrophenyl)succinic Acid

Ref: TR-N901493

Butanedioic acid, 2-(4-nitrophenyl)-

Ref: IN-DA002KND