Benzenepentanoic acid, α-amino- (CAS 34993-02-7) is an organic compound characterized by its structure, which includes a benzene ring attached to a pentanoic acid chain with an amino group at the alpha position. This compound features both carboxylic acid and amino functional groups, making it an amino acid derivative. Its molecular structure contributes to its potential as a building block in the synthesis of various pharmaceuticals and biochemicals. The presence of the benzene ring imparts aromatic properties, while the pentanoic acid chain provides hydrophobic characteristics. The amino group allows for interactions typical of amino acids, such as forming peptide bonds. This compound may exhibit both acidic and basic properties, depending on the pH of the environment, and can participate in various chemical reactions, including esterification and amidation. Its solubility in polar solvents is influenced by the carboxylic acid and amino groups, while the aromatic ring may enhance its stability and reactivity in organic synthesis.

Benzenepentanoic acid, a-amino-

34993-02-7: Benzenepentanoicacid, a-amino-, (?à)-, (?à)-2-Amino-5-phenylpentanoic acid, 2-Amino-5-phenylvaleric acid, DL-2-Amino-5-phenylpentanoic acid, Nsc 167401

Benzenepentanoic acid, α-amino-

D-2-Amino-5-phenylpentanoic acid is an analog of the natural amino acid β-amino acid. It is a cyclodepsipeptide that is synthesized by the synthetic route, through the use of hydrochloric acid, hydrogenated, and saponified. D-2-Amino-5-phenylpentanoic acid has been used as a monomer in asymmetric synthesis to produce a variety of analogs with varying substituents on its phenyl ring. This amino acid has also been shown to inhibit the growth of fungi and bacteria.

CAS 34993-02-7: Benzenepentanoic acid, a-amino-

Benzenepentanoic acid, α-amino-

Ref: IN-DA0029LG

D-2-Amino-5-phenylpentanoic acid

Ref: 3D-FA50359

2-Amino-5-phenylpentanoic acid

Ref: 10-F232603