2-Amino-3-(4-bromobenzoyl)benzoic acid, with the CAS number 241496-82-2, is an organic compound characterized by its aromatic structure and functional groups. It features an amino group (-NH2) and a carboxylic acid group (-COOH), which contribute to its acidic properties. The presence of a bromobenzoyl substituent enhances its reactivity and may influence its biological activity. This compound is typically a solid at room temperature and may exhibit moderate solubility in polar solvents due to the presence of the carboxylic acid group. Its molecular structure suggests potential applications in pharmaceuticals, particularly in the development of drugs targeting specific biological pathways. The bromine atom can also impart unique electronic properties, making it a candidate for further chemical modifications. Additionally, the compound's characteristics, such as melting point, boiling point, and spectral properties, can be determined through standard analytical techniques like NMR, IR spectroscopy, and mass spectrometry, which are essential for confirming its identity and purity in research and industrial applications.

2-amino-3-(4-bromobenzoyl)benzoic acid

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Bromfenac Impurity 4

Applications 2-Amino-3-(4-bromobenzoyl)benzoic Acid is a metabolite of Bromfenac sodium (B678550).
References Walsh, D.A., et al.: J. Med. Chem., 25, 446 (1982),


2-Amino-3-(4-bromobenzoyl)benzoic Acid

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CAS 241496-82-2: 2-amino-3-(4-bromobenzoyl)benzoic acid

Bromfenac Impurity 4

Ref: ST-EA-CP-B18006

2-Amino-3-(4-bromobenzoyl)benzoic Acid

Ref: TR-A593840

2-Amino-3-(4-bromobenzoyl)benzoic Acid

Ref: IN-DA003GCQ

2-Amino-3-(4-bromobenzoyl)benzoic acid

Ref: 3D-FA183121

Bromfenac Impurity 4 Sodium Salt

Ref: 4Z-B-478