2-Amino-3,5-dibromo-6-chlorobenzoic acid is an aromatic compound characterized by the presence of both amino and carboxylic acid functional groups, which contribute to its acidic properties. The molecule features a benzene ring substituted with two bromine atoms and one chlorine atom, which are halogen substituents that can influence the compound's reactivity and stability. The amino group (-NH2) is a basic functional group that can participate in hydrogen bonding, enhancing the compound's solubility in polar solvents. The presence of multiple halogens can also affect the compound's electronic properties, making it potentially useful in various chemical reactions, including nucleophilic substitutions. This compound may exhibit biological activity, making it of interest in pharmaceutical research. Its unique structure allows for potential applications in agrochemicals or as intermediates in organic synthesis. Overall, the combination of functional groups and halogen substituents makes 2-amino-3,5-dibromo-6-chlorobenzoic acid a compound of significant interest in both synthetic and medicinal chemistry.

2-amino-3,5-dibromo-6-chlorobenzoic acid

143769-25-9: 2-Amino-3,5-dibromo-6-chlorobenzoic acid is an aromatic compound characterized by the presence of both amino and carboxylic acid functional groups, which contribute to its acidic properties. The molecule features a benzene ring substituted with two bromine atoms and one chlorine atom, which are halogen substituents that can influence the compound's reactivity and stability. The amino group (-NH2) is a basic functional group that can participate in hydrogen bonding, enhancing the compound's solubility in polar solvents. The presence of multiple halogens can also affect the compound's electronic properties, making it potentially useful in various chemical reactions, including nucleophilic substitutions. This compound may exhibit biological activity, making it of interest in pharmaceutical research. Its unique structure allows for potential applications in agrochemicals or as intermediates in organic synthesis. Overall, the combination of functional groups and halogen substituents makes 2-amino-3,5-dibromo-6-chlorobenzoic acid a compound of significant interest in both synthetic and medicinal chemistry.

CAS 143769-25-9

2-amino-3,5-dibromo-6-chlorobenzoic acid

2-Amino-3,5-dibromo-6-chlorobenzoic acid

Ref: IN-DA001IBU

2-Amino-6-chloro-3,5-dibromobenzoic acid

Ref: 54-OR4663