2-Amino-2-(4-methylphenyl)acetic acid, commonly known as 4-methylphenylalanine, is an amino acid derivative characterized by the presence of an amino group (-NH2) and a carboxylic acid group (-COOH) attached to a carbon backbone. This compound features a 4-methylphenyl group, which contributes to its hydrophobic characteristics, making it less soluble in water compared to more polar amino acids. It is a chiral molecule, existing in two enantiomeric forms, which can have different biological activities. The presence of the aromatic ring enhances its stability and can influence its interactions in biological systems. 2-Amino-2-(4-methylphenyl)acetic acid is often studied in the context of protein synthesis and can serve as a building block in peptide synthesis. Its CAS number, 13227-01-5, is a unique identifier used for regulatory and safety purposes. Overall, this compound plays a significant role in biochemical research and has potential applications in pharmaceuticals and biotechnology.

2-AMINO-2-(4-Methylphenyl)ACETIC ACID

13227-01-5: 4-Methylphenyl glycine, Amino(4-Methylphenyl)ACETIC ACID, Amino-P-TOLYL-ACETIC ACID, DL-4-Methylphenylglycine, 4-Methylphenylglycine, Rarechem Ak Ml 0528, N-(4-methylphenyl)glycine

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CAS 13227-01-5: 2-AMINO-2-(4-Methylphenyl)ACETIC ACID

2-Amino-2-(4-methylphenyl)acetic acid

Ref: 3D-FM43592

Benzeneacetic acid, α-amino-4-methyl-

Ref: IN-DA0010GQ

2-Amino-2-(4-methylphenyl)acetic acid

Ref: 54-OR53059

DL-4-Methylphenylglycine

Ref: 10-F040245