Amino-(3-fluoro-phenyl)-acetic acid hydrochloride, identified by its CAS number 1137474-81-7, is a chemical compound that features an amino group, a phenyl ring substituted with a fluorine atom at the meta position, and an acetic acid moiety. This compound typically exists as a hydrochloride salt, which enhances its solubility in water and makes it suitable for various applications in pharmaceuticals and biochemistry. The presence of the amino group suggests that it can participate in various chemical reactions, including peptide bond formation, making it relevant in the synthesis of amino acid derivatives or pharmaceuticals. The fluorine substitution on the phenyl ring may influence the compound's biological activity, potentially enhancing its lipophilicity or altering its interaction with biological targets. As with many amino acids and their derivatives, it may exhibit zwitterionic behavior, depending on the pH of the solution. Overall, this compound's unique structure and properties make it a subject of interest in medicinal chemistry and drug development.

AMINO-(3-FLUORO-PHENYL)-ACETIC ACID HCL

1137474-81-7: Amino-(3-fluoro-phenyl)-acetic acid hydrochloride, identified by its CAS number 1137474-81-7, is a chemical compound that features an amino group, a phenyl ring substituted with a fluorine atom at the meta position, and an acetic acid moiety. This compound typically exists as a hydrochloride salt, which enhances its solubility in water and makes it suitable for various applications in pharmaceuticals and biochemistry. The presence of the amino group suggests that it can participate in various chemical reactions, including peptide bond formation, making it relevant in the synthesis of amino acid derivatives or pharmaceuticals. The fluorine substitution on the phenyl ring may influence the compound's biological activity, potentially enhancing its lipophilicity or altering its interaction with biological targets. As with many amino acids and their derivatives, it may exhibit zwitterionic behavior, depending on the pH of the solution. Overall, this compound's unique structure and properties make it a subject of interest in medicinal chemistry and drug development.

CAS 1137474-81-7

AMINO-(3-FLUORO-PHENYL)-ACETIC ACID HCL

2-Amino-2-(3-fluorophenyl)acetic acid, HCl

Ref: IN-DA0009J6