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CAS 63393-59-9

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(2R)-2-(acetylamino)-4-phenylbutanoic acid

Description:
(2R)-2-(Acetylamino)-4-phenylbutanoic acid, also known as phenylbutyric acid derivative, is an amino acid derivative characterized by its unique structure that includes an acetylamino group and a phenyl group attached to a butanoic acid backbone. This compound typically exhibits properties associated with both amino acids and carboxylic acids, such as the ability to form hydrogen bonds due to the presence of the carboxylic acid functional group and the amide bond from the acetylamino group. It is generally soluble in polar solvents, reflecting its polar functional groups, while the phenyl group contributes to its hydrophobic characteristics. The compound may exhibit biological activity, potentially influencing metabolic pathways or serving as a precursor in synthetic chemistry. Its stereochemistry, indicated by the (2R) designation, suggests specific spatial arrangements that can affect its reactivity and interaction with biological systems. Overall, this compound is of interest in pharmaceutical and biochemical research, particularly in the context of drug design and development.
Formula:C12H15NO3
InChI:InChI=1/C12H15NO3/c1-9(14)13-11(12(15)16)8-7-10-5-3-2-4-6-10/h2-6,11H,7-8H2,1H3,(H,13,14)(H,15,16)/t11-/m1/s1
SMILES:CC(=N[C@H](CCc1ccccc1)C(=O)O)O
Synonyms:
  • (2R)-2-acetamido-4-phenylbutanoic acid
  • benzenebutanoic acid, alpha-(acetylamino)-, (alphaR)-
  • Acetyl-D-homophenylalanine
  • Ac-D-Hph-OH
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