(R)-Amino-(3-fluoro-phenyl)-acetic acid, commonly referred to as a fluorinated amino acid, is an organic compound characterized by the presence of both an amino group and a carboxylic acid group, making it an α-amino acid. The presence of a fluorine atom on the phenyl ring enhances its biochemical properties, potentially influencing its interactions with biological systems. This compound is typically used in pharmaceutical research and development, particularly in the synthesis of biologically active molecules or as a building block in drug design. Its chirality, indicated by the (R) configuration, suggests that it may exhibit specific stereochemical properties that can affect its biological activity and receptor interactions. The compound is soluble in polar solvents, and its stability can be influenced by pH and temperature. As with many amino acids, it may participate in various chemical reactions, including peptide bond formation, making it relevant in the study of protein synthesis and function. Safety data should be consulted for handling and usage, as with all chemical substances.

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

25698-44-6: (R)-Amino-(3-fluoro-phenyl)-acetic acid, commonly referred to as a fluorinated amino acid, is an organic compound characterized by the presence of both an amino group and a carboxylic acid group, making it an α-amino acid. The presence of a fluorine atom on the phenyl ring enhances its biochemical properties, potentially influencing its interactions with biological systems. This compound is typically used in pharmaceutical research and development, particularly in the synthesis of biologically active molecules or as a building block in drug design. Its chirality, indicated by the (R) configuration, suggests that it may exhibit specific stereochemical properties that can affect its biological activity and receptor interactions. The compound is soluble in polar solvents, and its stability can be influenced by pH and temperature. As with many amino acids, it may participate in various chemical reactions, including peptide bond formation, making it relevant in the study of protein synthesis and function. Safety data should be consulted for handling and usage, as with all chemical substances.

(R)-2-Amino-2-(3-fluorophenyl)acetic acid

CAS 25698-44-6

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

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

Ref: IN-DA00BCSN

(R)-2-Amino-2-(3-fluorophenyl)acetic acid

Ref: 54-PC103433

(R)-2-Amino-2-(3-fluorophenyl)acetic acid

Ref: 10-F693269