Amino-(3,5-difluoro-phenyl)-acetic acid, identified by its CAS number 199327-33-8, is an organic compound characterized by the presence of an amino group and an acetic acid moiety attached to a phenyl ring that is substituted with two fluorine atoms at the 3 and 5 positions. This compound typically exhibits properties associated with both amino acids and aromatic compounds, including potential solubility in polar solvents due to the amino and carboxylic acid functional groups. The presence of fluorine atoms can influence the compound's reactivity, stability, and biological activity, often enhancing lipophilicity and altering hydrogen bonding capabilities. As a derivative of phenylalanine, it may play a role in biochemical pathways or serve as a building block in pharmaceutical synthesis. Its unique structure may also confer specific interactions in biological systems, making it of interest in medicinal chemistry and drug development. Overall, amino-(3,5-difluoro-phenyl)-acetic acid represents a compound with diverse potential applications in research and industry.

AMINO-(3,5-DIFLUORO-PHENYL)-ACETIC ACID

199327-33-8: Amino-(3,5-difluoro-phenyl)-acetic acid, identified by its CAS number 199327-33-8, is an organic compound characterized by the presence of an amino group and an acetic acid moiety attached to a phenyl ring that is substituted with two fluorine atoms at the 3 and 5 positions. This compound typically exhibits properties associated with both amino acids and aromatic compounds, including potential solubility in polar solvents due to the amino and carboxylic acid functional groups. The presence of fluorine atoms can influence the compound's reactivity, stability, and biological activity, often enhancing lipophilicity and altering hydrogen bonding capabilities. As a derivative of phenylalanine, it may play a role in biochemical pathways or serve as a building block in pharmaceutical synthesis. Its unique structure may also confer specific interactions in biological systems, making it of interest in medicinal chemistry and drug development. Overall, amino-(3,5-difluoro-phenyl)-acetic acid represents a compound with diverse potential applications in research and industry.

CAS 199327-33-8

AMINO-(3,5-DIFLUORO-PHENYL)-ACETIC ACID

(2S)-2-Amino-2-(3,5-difluorophenyl)acetic acid

Ref: IN-DA002C2F

3,5-Difluoro-DL-phenylglycine

Ref: 54-PC6579