2-Amino-3-(2-bromo-phenyl)-propionic acid, with the CAS number 1991-79-3, is an amino acid derivative characterized by the presence of a bromine atom attached to a phenyl group at the 2-position of the aromatic ring. This compound features a propionic acid backbone, which includes an amino group (-NH2) and a carboxylic acid group (-COOH), making it a polar molecule with potential for hydrogen bonding. The bromine substitution introduces additional reactivity and influences the compound's physical and chemical properties, such as solubility and stability. Typically, such compounds are of interest in medicinal chemistry and biochemistry due to their potential biological activity and role as intermediates in the synthesis of pharmaceuticals. The presence of both the amino and carboxylic acid functional groups allows for various interactions in biological systems, making it a candidate for studies related to enzyme activity or receptor binding. Overall, 2-amino-3-(2-bromo-phenyl)-propionic acid exemplifies the complexity and utility of halogenated amino acids in chemical research.

2-AMINO-3-(2-BROMO-PHENYL)-PROPIONIC ACID

1991-79-3: 2-Amino-3-(2-bromo-phenyl)-propionic acid, with the CAS number 1991-79-3, is an amino acid derivative characterized by the presence of a bromine atom attached to a phenyl group at the 2-position of the aromatic ring. This compound features a propionic acid backbone, which includes an amino group (-NH2) and a carboxylic acid group (-COOH), making it a polar molecule with potential for hydrogen bonding. The bromine substitution introduces additional reactivity and influences the compound's physical and chemical properties, such as solubility and stability. Typically, such compounds are of interest in medicinal chemistry and biochemistry due to their potential biological activity and role as intermediates in the synthesis of pharmaceuticals. The presence of both the amino and carboxylic acid functional groups allows for various interactions in biological systems, making it a candidate for studies related to enzyme activity or receptor binding. Overall, 2-amino-3-(2-bromo-phenyl)-propionic acid exemplifies the complexity and utility of halogenated amino acids in chemical research.

CAS 1991-79-3

2-AMINO-3-(2-BROMO-PHENYL)-PROPIONIC ACID

Phenylalanine, 2-bromo-

Ref: IN-DA002BWC

2-Bromophenyl-DL-alanine

Ref: 54-OR480300

2-Amino-3-(2-bromophenyl)propanoic acid

Ref: 10-F224338