N-formyl-dl-phenylalanine is an amino acid derivative characterized by the presence of a formyl group (-CHO) attached to the nitrogen of the amino group in phenylalanine. This compound is a white to off-white solid that is soluble in polar solvents such as water and methanol, owing to its amino and carboxylic acid functional groups. It exhibits properties typical of amino acids, including the ability to participate in peptide bond formation, making it relevant in biochemical applications. The presence of the phenyl group contributes to its hydrophobic characteristics, influencing its interactions in biological systems. N-formyl-dl-phenylalanine is often used in research and pharmaceutical contexts, particularly in studies related to peptide synthesis and drug development. Its CAS number, 4289-95-6, is a unique identifier that facilitates the identification and procurement of this compound in scientific literature and databases. As with many amino acid derivatives, it may exhibit biological activity, making it of interest in various fields, including medicinal chemistry and biochemistry.

N-formyl-dl-phenylalanine

4289-95-6: N-formyl-dl-phenylalanine is an amino acid derivative characterized by the presence of a formyl group (-CHO) attached to the nitrogen of the amino group in phenylalanine. This compound is a white to off-white solid that is soluble in polar solvents such as water and methanol, owing to its amino and carboxylic acid functional groups. It exhibits properties typical of amino acids, including the ability to participate in peptide bond formation, making it relevant in biochemical applications. The presence of the phenyl group contributes to its hydrophobic characteristics, influencing its interactions in biological systems. N-formyl-dl-phenylalanine is often used in research and pharmaceutical contexts, particularly in studies related to peptide synthesis and drug development. Its CAS number, 4289-95-6, is a unique identifier that facilitates the identification and procurement of this compound in scientific literature and databases. As with many amino acid derivatives, it may exhibit biological activity, making it of interest in various fields, including medicinal chemistry and biochemistry.

CAS 4289-95-6

N-formyl-dl-phenylalanine

N-Formyl-DL-phenylalanine

Ref: 3B-F0126

N-FORMYL-DL-PHENYLALANINE

Ref: IN-DA003T1C

N-Formyl-DL-phenylalanine

Ref: 54-OR924498

2-Formamido-3-phenylpropanoic acid

Ref: 10-F692580