(S)-Amino-(3-fluoro-phenyl)-acetic acid, also known as (S)-3-fluoro-phenyl-alanine, is an amino acid derivative characterized by the presence of a fluorine atom on the aromatic ring. This compound features a chiral center, which contributes to its stereochemistry, specifically the S configuration. It is typically a white to off-white crystalline solid and is soluble in polar solvents such as water and alcohols, reflecting its polar nature due to the amino and carboxylic acid functional groups. The presence of the fluorine atom can influence the compound's biological activity and interactions, making it of interest in pharmaceutical research, particularly in the development of drugs targeting specific receptors or enzymes. Its molecular structure allows it to participate in various chemical reactions, including peptide bond formation, which is essential for protein synthesis. As with many amino acids, it may also exhibit zwitterionic behavior, possessing both positive and negative charges at physiological pH. Overall, (S)-amino-(3-fluoro-phenyl)-acetic acid is a significant compound in medicinal chemistry and biochemistry.

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

154006-66-3: (S)-Amino-(3-fluoro-phenyl)-acetic acid, also known as (S)-3-fluoro-phenyl-alanine, is an amino acid derivative characterized by the presence of a fluorine atom on the aromatic ring. This compound features a chiral center, which contributes to its stereochemistry, specifically the S configuration. It is typically a white to off-white crystalline solid and is soluble in polar solvents such as water and alcohols, reflecting its polar nature due to the amino and carboxylic acid functional groups. The presence of the fluorine atom can influence the compound's biological activity and interactions, making it of interest in pharmaceutical research, particularly in the development of drugs targeting specific receptors or enzymes. Its molecular structure allows it to participate in various chemical reactions, including peptide bond formation, which is essential for protein synthesis. As with many amino acids, it may also exhibit zwitterionic behavior, possessing both positive and negative charges at physiological pH. Overall, (S)-amino-(3-fluoro-phenyl)-acetic acid is a significant compound in medicinal chemistry and biochemistry.

CAS 154006-66-3

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

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

Ref: 54-PC520834

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

Ref: 10-F762744