2-Amino-3-bromo-5-chlorobenzoic acid is an aromatic amino acid derivative characterized by the presence of both amino and carboxylic acid functional groups, which contribute to its acidic properties. The compound features a benzene ring substituted with a bromine atom at the 3-position and a chlorine atom at the 5-position, along with an amino group at the 2-position. This substitution pattern influences its reactivity and solubility, making it polar and capable of forming hydrogen bonds. The presence of halogen substituents can also affect its biological activity and interaction with other molecules. Typically, compounds like this are of interest in pharmaceutical chemistry and materials science due to their potential applications in drug development and synthesis of complex organic molecules. Additionally, the compound's structure allows for various synthetic modifications, which can lead to derivatives with enhanced properties or activities. Safety data should be consulted for handling, as halogenated compounds can pose specific health risks.

2-Amino-3-bromo-5-chlorobenzoic acid

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Applications 2-Amino-3-bromo-5-chlorobenzoic Acid is used as a starting material in the synthesis of a series of 3-(2-(2-methoxyphenyl)-2-oxoethyl) quinazolinone derivatives, which showed anticoccidial activity against Eimeria tenella in chicken.
References Ye, Changwen., et al.: Pestic. Biochem. Phys., 97(3), 194-198 (2010)


CAS 41198-02-1: 2-Amino-3-bromo-5-chlorobenzoic acid

2-Amino-3-bromo-5-chlorobenzoic Acid

Ref: TR-A602015

2-Amino-3-bromo-5-chlorobenzoic acid

Ref: 3D-RBA19802

2-Amino-3-bromo-5-chlorobenzoic acid

Ref: 10-F037617

2-Amino-3-bromo-5-chlorobenzoic acid

Ref: 54-OR46070

Benzoic acid, 2-aMino-3-broMo-5-chloro-

Ref: IN-DA00C9RA