142312-21-8

Basic information

• Product Name: N-(4-methoxybenzoyl)-2-(4-methylphenyl)glycine
• Synonyms: N-(4-methoxybenzoyl)-2-(4-methylphenyl)glycine
• CAS NO: 142312-21-8
• Molecular Weight: 299.326
• Mol File: 142312-21-8.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: N-(4-methoxybenzoyl)-2-(4-methylphenyl)glycine(CAS DataBase Reference)
• NIST Chemistry Reference: N-(4-methoxybenzoyl)-2-(4-methylphenyl)glycine(142312-21-8)
• EPA Substance Registry System: N-(4-methoxybenzoyl)-2-(4-methylphenyl)glycine(142312-21-8)

Safety Data

• Hazardous Substances Data: 142312-21-8(Hazardous Substances Data)

Upstream product

• 137321-01-8 methyl 2-((diphenylmethylene)amino)-2-(p-tolyl)acetate 
• 137321-00-7 Amino-p-tolyl-acetic acid methyl ester 
• 13227-01-5 2-amino-2-(4-methylphenyl)acetic acid 
• 100-07-2 4-methoxy-benzoyl chloride 

Downstream Products

• 142312-20-7 2-(4-methoxyphenyl)-4-(p-tolyl)oxazol-5(4H)-one 
• 94863-18-0 1,3-diphenyl-5-(p-tolyl)-1H-1,2,4-triazole 
• 1049-17-8 5-(4-methoxyphenyl)-1,3-diphenyl-1H-1,2,4-triazole 
• 142312-22-9 2,3-Bis-(4-methoxy-phenyl)-5,6-di-p-tolyl-pyrazine 
• 142312-24-1 3,5-Bis-(4-methoxy-phenyl)-1-p-tolyl-1H-[1,2,4]triazole 
• 142312-25-2 3-(4-Methoxy-phenyl)-1,5-di-p-tolyl-1H-[1,2,4]triazole 
• 17555-94-1 (E)-4'-methoxy-4-methylstilbene 
• 142312-02-5 2-(4-methoxyphenyl)-4-(4-methylphenyl)-5(4H)oxazolone 

Relevant articles and documents

Catalytic Aerobic Cross-Dehydrogenative Coupling of Azlactones en Route to α,α-Disubstituted α-Amino Acids

We developed a catalytic aerobic method to synthesize α,α-disubstituted α-amino acids through cross-dehydrogenative coupling of azlactones. Combining an iron catalyst with a bisoxazolidine ligand resulted in high catalytic performance, and cross-coupling with an indole proceeded smoothly under aerobic conditions. A wide variety of α-aryl and aliphatic amino acid derived azlactones were applied to the present catalysis. In addition, a quaternary carbon could be constructed using oxindole and benzofuranone under aerobic conditions.

OXAZOLONES. PART VI. REACTION OF 5(4H)-OXAZOLONES WITH NITRILE IMINES: SYNTHESIS OF 1H-1,2,4-TRIAZOLES THROUGH CYCLOADDITION

5(4H)-Oxazolones (1) react as dipolarophiles in cycloadditions with nitrile imines generated from tetrazoles (2) in refluxing anisole affording two 1H-1,2,4-triazole derivatives (3) and diarylethylenes (4).