(±)-A-methyl-(4-tetrazolylphenyl)glycine, identified by CAS number 169209-66-9, is a chemical compound that belongs to the class of amino acids and is characterized by the presence of a tetrazole ring and a phenyl group. This compound exhibits both chiral properties, as indicated by the (±) notation, suggesting the presence of enantiomers. The tetrazole moiety contributes to its potential biological activity, often enhancing solubility and stability. The presence of the methyl group at the alpha position relative to the carboxylic acid functional group is significant for its interaction with biological targets, potentially influencing its pharmacological properties. This compound may be of interest in medicinal chemistry and drug development, particularly in the context of neuropharmacology or as a building block for more complex molecules. Its synthesis and characterization would typically involve standard organic chemistry techniques, and its properties can be further explored through various analytical methods such as NMR, mass spectrometry, and chromatography.

(+-)-A-methyl-(4-tetrazolylphenyl)*glycine

169209-66-9: (±)-A-methyl-(4-tetrazolylphenyl)glycine, identified by CAS number 169209-66-9, is a chemical compound that belongs to the class of amino acids and is characterized by the presence of a tetrazole ring and a phenyl group. This compound exhibits both chiral properties, as indicated by the (±) notation, suggesting the presence of enantiomers. The tetrazole moiety contributes to its potential biological activity, often enhancing solubility and stability. The presence of the methyl group at the alpha position relative to the carboxylic acid functional group is significant for its interaction with biological targets, potentially influencing its pharmacological properties. This compound may be of interest in medicinal chemistry and drug development, particularly in the context of neuropharmacology or as a building block for more complex molecules. Its synthesis and characterization would typically involve standard organic chemistry techniques, and its properties can be further explored through various analytical methods such as NMR, mass spectrometry, and chromatography.

2-(4-(1H-Tetrazol-5-yl)phenyl)-2-aminopropanoic acid

Group II/group III metabotropic glutamate receptor antagonist

CAS 169209-66-9

(+-)-A-methyl-(4-tetrazolylphenyl)*glycine

2-(4-(1H-Tetrazol-5-yl)phenyl)-2-aminopropanoic acid

Ref: IN-DA001YL2

MTPG

Ref: TM-T23033