Benzenebutanoic acid, α-amino-, methyl ester, (S)-, also known by its CAS number 106860-17-7, is an organic compound characterized by its chiral α-amino acid structure. This compound features a benzenebutanoic acid backbone, which includes a benzene ring attached to a butanoic acid chain, with an amino group and a methyl ester functional group. The (S)- designation indicates that it has a specific stereochemistry, which is crucial for its biological activity and interactions. This compound is typically soluble in organic solvents and may exhibit moderate solubility in water, depending on the pH and the presence of other functional groups. Its properties make it relevant in pharmaceutical applications, particularly in the synthesis of biologically active molecules. The presence of both the amino and ester functionalities allows for various chemical reactions, including peptide bond formation and ester hydrolysis, making it a versatile intermediate in organic synthesis. Overall, its unique structure and properties contribute to its significance in medicinal chemistry and related fields.

Benzenebutanoic acid, a-amino-, methyl ester, (S)-

106860-17-7: Benzenebutanoic acid, α-amino-, methyl ester, (S)-, also known by its CAS number 106860-17-7, is an organic compound characterized by its chiral α-amino acid structure. This compound features a benzenebutanoic acid backbone, which includes a benzene ring attached to a butanoic acid chain, with an amino group and a methyl ester functional group. The (S)- designation indicates that it has a specific stereochemistry, which is crucial for its biological activity and interactions. This compound is typically soluble in organic solvents and may exhibit moderate solubility in water, depending on the pH and the presence of other functional groups. Its properties make it relevant in pharmaceutical applications, particularly in the synthesis of biologically active molecules. The presence of both the amino and ester functionalities allows for various chemical reactions, including peptide bond formation and ester hydrolysis, making it a versatile intermediate in organic synthesis. Overall, its unique structure and properties contribute to its significance in medicinal chemistry and related fields.

<p>Methyl (2s)-2-amino-4-phenylbutanoate</p>

CAS 106860-17-7

Benzenebutanoic acid, a-amino-, methyl ester, (S)-

Methyl (2s)-2-amino-4-phenylbutanoate

Ref: 54-OR955609

L-Homophenylalanine Methyl Ester

Ref: TR-H600505