39696-58-7

Usage

Family

Triazole

Uses

Intermediate in the synthesis of pharmaceuticals, agrochemicals, and dyes

Potential Applications

Antifungal and antimicrobial agent, corrosion inhibitor

Physical Appearance

White to off-white crystalline powder

Stability

Relatively stable under normal conditions

Reactivity

Largely determined by the substituents on the phenyl ring

Versatility

Wide range of potential uses in various industries

Upstream product

• 186581-53-3 diazomethane 
• 3357-42-4 3-phenyl-1,2,4-triazole 
• 74-88-4 methyl iodide 
• 64-18-6 formic acid 
• 40994-01-2 N-methyl-benzamidrazone 
• 83274-32-2 N²-Methylbenzamidrazoniumiodid 
• 180901-61-5 1-methyl-3-phenyl-4,5-dihydro-1,2,4-triazin-6(1H)-one 
• 13466-29-0 1-benzylidene-2-methylhydrazine 
• 127-19-5 N,N-dimethyl acetamide 
• 1670-14-0 benzamidine monohydrochloride 
• 68-12-2 N,N-dimethyl-formamide 
• 5333-86-8 ethyl benzimidate hydrochloride 
• 4252-31-7 N-formylbenzamide 
• 37067-45-1 N¹,S-Dimethylthiobenzohydrazoniumiodid 

Relevant academic research and scientific papers

Copper-Catalyzed Oxidative C(sp3)-H Functionalization for Facile Synthesis of 1,2,4-Triazoles and 1,3,5-Triazines from Amidines

A facile and versatile catalytic system involving copper catalyst, K3PO4 as the base, and O2 as the oxidant has been developed to enable efficient synthesis of 2,4,6-trisubstituted and 2,6-disubstituted 1,3,5-triazines and

Dihydro-1,2,4-triazin-6(1H)-ones. III oxidation products of 1-Methyl-3-phenyl-4,5-dihydro-1,2,4-triazin-6(1H)-one

1-Methyl-3-phenyl-4,5-dihydro-1,2,4-triazin-6(1H)-one (1) undergoes aerial oxidation to give a mixture of 1-methyl-3-phenyl-1,2,4-triazin-6(1H)-one (2) and 1-methyl-3-phenyl-1,4-dihydro-1,2,4-triazine-5,6-dione (3). The dehydro derivative (2) was cleanly

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

Synthesis of 1,2,4-Triazines, IX. Synthesis of Cyclopenta-1,2,4-triazines

Derivatives 12a - f and 23a - c of hitherto unknown cyclopenta-1,2,4-triazine system 1 were prepared from cyclopentadienedicarboxylates 9a,b and amidrazones 10a - d or 14a - c, respectively.