Amino(3,4-difluorophenyl)acetic acid, with the CAS number 225641-94-1, is an organic compound characterized by the presence of an amino group and a carboxylic acid functional group attached to a phenyl ring that has two fluorine substituents at the 3 and 4 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 groups. The presence of fluorine atoms can influence its reactivity and biological activity, often enhancing lipophilicity and altering hydrogen bonding capabilities. The compound may be of interest in pharmaceutical research, particularly in the development of drugs targeting specific biological pathways. Its structural features suggest potential applications in medicinal chemistry, where modifications to the phenyl ring can lead to variations in pharmacological properties. As with many fluorinated compounds, it may also exhibit unique physical and chemical properties, such as altered melting and boiling points compared to its non-fluorinated counterparts.

amino(3,4-difluorophenyl)acetic acid

225641-94-1: Amino(3,4-difluorophenyl)acetic acid, with the CAS number 225641-94-1, is an organic compound characterized by the presence of an amino group and a carboxylic acid functional group attached to a phenyl ring that has two fluorine substituents at the 3 and 4 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 groups. The presence of fluorine atoms can influence its reactivity and biological activity, often enhancing lipophilicity and altering hydrogen bonding capabilities. The compound may be of interest in pharmaceutical research, particularly in the development of drugs targeting specific biological pathways. Its structural features suggest potential applications in medicinal chemistry, where modifications to the phenyl ring can lead to variations in pharmacological properties. As with many fluorinated compounds, it may also exhibit unique physical and chemical properties, such as altered melting and boiling points compared to its non-fluorinated counterparts.

CAS 225641-94-1

amino(3,4-difluorophenyl)acetic acid

3,4-Difluorophenylglycine

Ref: IN-DA00BFGA

3,4-Difluoro-DL-phenylglycine

Ref: 54-PC7856

3,4-Difluorophenylglycine

Ref: 10-F007879