The chemical properties of 2-Amino-4,6-dichlorobenzoic Acid, bearing the CAS number 20776-63-0, are fundamental to its widespread utility in various synthetic processes. Typically appearing as an off-white to white powder, this compound possesses a molecular formula of C7H5Cl2NO2 and a molecular weight of approximately 206.03 g/mol. Its structure features an amino group (-NH2) and two chlorine atoms (-Cl) attached to a benzoic acid core. This specific arrangement dictates its reactivity and suitability for diverse applications, from pharmaceutical intermediate synthesis to the creation of dyes and pigments.

Key to its application is the presence of reactive functional groups. The amino group can readily participate in nucleophilic substitution and acylation reactions, while the carboxylic acid group (-COOH) can undergo esterification and amide formation. The electron-withdrawing nature of the chlorine atoms influences the acidity of the carboxylic acid and the reactivity of the aromatic ring towards electrophilic substitution. Understanding these CAS 20776-63-0 properties is crucial for chemists when designing synthetic strategies. The efficiency of its 2-Amino-4,6-dichlorobenzoic Acid synthesis is also a testament to its well-defined chemical behavior.

Furthermore, investigations into the biological activity of dichlorobenzoic acid derivatives often leverage these intrinsic chemical properties to tailor molecules for specific biological targets. This ability to undergo controlled chemical modifications makes 2-Amino-4,6-dichlorobenzoic Acid an indispensable tool in both academic research and industrial applications, underpinning its importance in chemical synthesis and beyond.