Benzenepropanamide, α-amino-N-methyl-N-phenyl-, (S)-, also known by its CAS number 124287-48-5, is a chiral compound characterized by its amide functional group and a phenyl ring attached to a propanamide backbone. This compound features a methyl and a phenyl group attached to the nitrogen atom, contributing to its unique properties. As an amino acid derivative, it exhibits both hydrophilic and hydrophobic characteristics, which can influence its solubility in various solvents. The presence of the chiral center indicates that it can exist in two enantiomeric forms, with the (S)- configuration being one of them, which may have implications for its biological activity and interactions. This compound may be of interest in pharmaceutical research due to its potential applications in drug development, particularly in the design of compounds that target specific biological pathways. Its stability, reactivity, and interactions with other molecules can be influenced by the presence of the amide and amino groups, making it a subject of study in organic and medicinal chemistry.

Benzenepropanamide, a-amino-N-methyl-N-phenyl-, (S)-

124287-48-5: Benzenepropanamide, α-amino-N-methyl-N-phenyl-, (S)-, also known by its CAS number 124287-48-5, is a chiral compound characterized by its amide functional group and a phenyl ring attached to a propanamide backbone. This compound features a methyl and a phenyl group attached to the nitrogen atom, contributing to its unique properties. As an amino acid derivative, it exhibits both hydrophilic and hydrophobic characteristics, which can influence its solubility in various solvents. The presence of the chiral center indicates that it can exist in two enantiomeric forms, with the (S)- configuration being one of them, which may have implications for its biological activity and interactions. This compound may be of interest in pharmaceutical research due to its potential applications in drug development, particularly in the design of compounds that target specific biological pathways. Its stability, reactivity, and interactions with other molecules can be influenced by the presence of the amide and amino groups, making it a subject of study in organic and medicinal chemistry.

CAS 124287-48-5

Benzenepropanamide, a-amino-N-methyl-N-phenyl-, (S)-