(R)-2-Acetamido-2-(2-fluorophenyl)propanoic acid, commonly referred to by its CAS number 320-58-1, is an amino acid derivative characterized by the presence of an acetamido group and a fluorophenyl substituent on a propanoic acid backbone. This compound exhibits both acidic and basic properties due to the carboxylic acid functional group and the amide functionality, making it a zwitterionic species in solution. The fluorine atom in the phenyl ring can influence the compound's electronic properties, potentially enhancing its biological activity or altering its interaction with biological targets. The stereochemistry indicated by the (R) configuration suggests a specific spatial arrangement of atoms, which can be crucial for its biological function and pharmacological profile. This compound may be of interest in medicinal chemistry, particularly in the development of pharmaceuticals, due to its potential role as an enzyme inhibitor or in other therapeutic applications. Its solubility, stability, and reactivity can vary based on environmental conditions, making it important to consider these factors in practical applications.

(R)-2-acetaMido-2-(2-fluorophenyl)propanoic acid

320-58-1: (R)-2-Acetamido-2-(2-fluorophenyl)propanoic acid, commonly referred to by its CAS number 320-58-1, is an amino acid derivative characterized by the presence of an acetamido group and a fluorophenyl substituent on a propanoic acid backbone. This compound exhibits both acidic and basic properties due to the carboxylic acid functional group and the amide functionality, making it a zwitterionic species in solution. The fluorine atom in the phenyl ring can influence the compound's electronic properties, potentially enhancing its biological activity or altering its interaction with biological targets. The stereochemistry indicated by the (R) configuration suggests a specific spatial arrangement of atoms, which can be crucial for its biological function and pharmacological profile. This compound may be of interest in medicinal chemistry, particularly in the development of pharmaceuticals, due to its potential role as an enzyme inhibitor or in other therapeutic applications. Its solubility, stability, and reactivity can vary based on environmental conditions, making it important to consider these factors in practical applications.

CAS 320-58-1

(R)-2-acetaMido-2-(2-fluorophenyl)propanoic acid

2-Amino-2-(2-fluorophenyl)propanoic acid

Ref: IN-DA01AFJO

2-Amino-2-(2-fluorophenyl)propanoic acid

Ref: 54-PC110340

2-Amino-2-(2-fluorophenyl)propanoic acid

Ref: 10-F552956

2-Amino-2-(2-fluorophenyl)propanoic acid

Ref: 3D-AAA32058