CAS 15727-49-8

Alanine, N-phenyl-

Description:

Alanine, N-phenyl- (CAS 15727-49-8) is an amino acid derivative characterized by the presence of a phenyl group attached to the nitrogen atom of the alanine structure. This compound exhibits properties typical of amino acids, including the ability to participate in hydrogen bonding due to its amino and carboxyl functional groups. The phenyl substitution can influence its solubility, stability, and reactivity, often making it less polar than standard alanine. N-phenyl-alanine may exhibit unique biological activities, potentially acting as a building block in peptide synthesis or as a ligand in various biochemical applications. Its structural features may also allow it to interact with specific receptors or enzymes, making it of interest in medicinal chemistry and drug design. Additionally, the compound's physical properties, such as melting point and boiling point, can vary based on its molecular interactions and the presence of other substituents. Overall, N-phenyl-alanine serves as a versatile compound in both synthetic and biological chemistry contexts.

Formula: C₉H₁₁NO₂

Alanine, N-phenyl-

CAS: 15727-49-8

Formula: C₉H₁₁NO₂

Purity: 97%

Color and Shape: Solid

Molecular weight: 165.1891

Ref: IN-DA001PCK

2-(Phenylamino)propanoic acid

CAS: 15727-49-8

2-(Phenylamino)propanoic acid

Purity: 97%

Molecular weight: 165.19g/mol

Ref: 54-OR1069654

2-Phenylamino-propionic acid

CAS: 15727-49-8

Formula: C₉H₁₁NO₂

Purity: 95.0%

Color and Shape: Solid

Molecular weight: 165.192

Ref: 10-F020221

2-Phenylamino-propionic acid

CAS: 15727-49-8

2-Phenylamino-propionic acid is an analogue of acrylic acid with two methyl groups on the terminal carbon. It is a colorless liquid that can be synthesized by the reaction of acrylic acid with sodium amide in the presence of benzene. 2-Phenylamino-propionic acid has been shown to undergo homogeneous and cyclic reactions, as well as elimination and monoxide reactions. The experimental value obtained for its rate constant, k, was found to be 1.6 × 10^6 L/mol*s using acrylic acid as a substrate. This product may also be used as a catalyst for radical reactions or in catalytic pyrolysis reactions.

Formula: C₉H₁₁NO₂

Purity: Min. 95%

Molecular weight: 165.19 g/mol

Ref: 3D-QAA72749