87277-51-8

Upstream product

• 623-03-0 4-Cyanochlorobenzene 
• 20743-49-1 2-methyl-5-phenyl-2H-tetrazole 
• 87436-46-2 4-Chloro-N-[1-ethoxy-1-phenyl-meth-(Z)-ylidene]-benzamide 
• 60-34-4 methylhydrazine 
• 825-60-5 benzimidic acid ethyl ester 
• 122-01-0 4-chloro-benzoyl chloride 
• 6828-55-3 N'-benzoyl-4′-chlorobenzohydrazide 
• 613-94-5 benzoic acid hydrazide 
• 87277-53-0 3-(4-chlorophenyl)-5-phenyl-1H-1,2,4-triazole 
• 74-88-4 methyl iodide 
• 471910-33-5 3-(4-chlorophenyl)-4-methyl-5-phenyl-4H-1,2,4-triazole 

Relevant academic research and scientific papers

Regioselectivity in the thermal rearrangement of unsymmetrical 4-methyl-4H-1,2,4-triazoles to 1-methyl-1H-1,2,4-triazoles

The rearrangement of 4-methyl-3,5-diaryl-4H-1,2,4-triazoles to the corresponding 1-methyl-3,5-diaryl-1H-1,2,4-triazoles showed regioselectivity comparable to that observed for the alkylation of 3,5-diaryl-1H-1,2,4-triazoles. This lends support to a proposed mechanism for the rearrangement that involves consecutive nucleophilic displacements steps.

1,3-Dipolar Cycloadditions, 91. The Chemistry of N-Methyl-C-phenylnitrilimine

The treatment of N'--N-methylhydrazinium bromide, accessible by bromination of benzaldehyde-N-methylhydrazone, with triethylamine furnishes the title compound; this method is superior to the thermolysis and photolysis of 2-methyl-5-phe