Benzyl 2-amino-4-phenyl-butanoate, also known as 4-methylbenzenesulfonic acid, is a chemical compound characterized by its complex structure, which includes an amino group, a phenyl group, and an ester functional group. This compound typically exhibits properties associated with both amines and esters, such as potential solubility in organic solvents and the ability to participate in various chemical reactions, including nucleophilic substitutions and acylation. The presence of the benzyl group contributes to its hydrophobic characteristics, while the amino group can engage in hydrogen bonding, influencing its reactivity and interaction with other molecules. Additionally, the sulfonic acid moiety enhances its acidity and can facilitate the formation of salts. This compound may be utilized in pharmaceutical applications, particularly in the synthesis of biologically active molecules, due to its functional groups that allow for further chemical modifications. Safety and handling precautions should be observed, as with many organic compounds, to mitigate any potential hazards associated with its use.

benzyl 2-amino-4-phenyl-butanoate; 4-methylbenzenesulfonic acid

117560-24-4: Benzyl 2-amino-4-phenyl-butanoate, also known as 4-methylbenzenesulfonic acid, is a chemical compound characterized by its complex structure, which includes an amino group, a phenyl group, and an ester functional group. This compound typically exhibits properties associated with both amines and esters, such as potential solubility in organic solvents and the ability to participate in various chemical reactions, including nucleophilic substitutions and acylation. The presence of the benzyl group contributes to its hydrophobic characteristics, while the amino group can engage in hydrogen bonding, influencing its reactivity and interaction with other molecules. Additionally, the sulfonic acid moiety enhances its acidity and can facilitate the formation of salts. This compound may be utilized in pharmaceutical applications, particularly in the synthesis of biologically active molecules, due to its functional groups that allow for further chemical modifications. Safety and handling precautions should be observed, as with many organic compounds, to mitigate any potential hazards associated with its use.

(2S)-2-Amino-benzenebutanoic acid benzyl ester tosylate salt

<p>Applications An intermediate in the preparation of Imidaprilat<br>References Hayashi, K., et al.: J. Med. Chem., 32, 289 (1989),<br></p>

CAS 117560-24-4

benzyl 2-amino-4-phenyl-butanoate; 4-methylbenzenesulfonic acid

(2S)-2-Amino-benzenebutanoic acid benzyl ester tosylate salt

Ref: 7W-GM7486

(2S)-2-Amino-benzenebutanoic Acid Benzyl Ester Tosylate Salt (>90%)

Ref: TR-A591420