D-Alanine, N-(phenylmethyl)-, also known as phenylmethyl D-alaninate, is an amino acid derivative characterized by the presence of a D-alanine backbone with a phenylmethyl (benzyl) group attached to the nitrogen atom of the amino group. This compound typically exhibits properties associated with amino acids, such as being a zwitterion at physiological pH, which means it can exist in both positively and negatively charged forms. It is soluble in polar solvents due to the presence of the amino and carboxyl functional groups, while the phenylmethyl group contributes to its hydrophobic characteristics. The compound may participate in various biochemical processes, including protein synthesis and enzyme activity modulation, due to its structural similarity to natural amino acids. Its unique structure may also influence its interactions with biological systems, making it of interest in pharmaceutical and biochemical research. As with many amino acid derivatives, it may exhibit specific optical activity, reflecting its chiral nature.

D-Alanine, N-(phenylmethyl)-

65491-01-2: D-Alanine, N-(phenylmethyl)-, also known as phenylmethyl D-alaninate, is an amino acid derivative characterized by the presence of a D-alanine backbone with a phenylmethyl (benzyl) group attached to the nitrogen atom of the amino group. This compound typically exhibits properties associated with amino acids, such as being a zwitterion at physiological pH, which means it can exist in both positively and negatively charged forms. It is soluble in polar solvents due to the presence of the amino and carboxyl functional groups, while the phenylmethyl group contributes to its hydrophobic characteristics. The compound may participate in various biochemical processes, including protein synthesis and enzyme activity modulation, due to its structural similarity to natural amino acids. Its unique structure may also influence its interactions with biological systems, making it of interest in pharmaceutical and biochemical research. As with many amino acid derivatives, it may exhibit specific optical activity, reflecting its chiral nature.

CAS 65491-01-2

D-Alanine, N-(phenylmethyl)-

(2R)-2-(Benzylamino)propanoic acid

Ref: 3D-QCA49101