39696-58-7

Basic information

• Product Name: 1-METHYL-3-PHENYL-1H-[1,2,4]TRIAZOLE
• Synonyms: 1-METHYL-3-PHENYL-1H-[1,2,4]TRIAZOLE
• CAS NO: 39696-58-7
• Molecular Formula: C₉H₉N₃
• Molecular Weight: 0
• Mol File: 39696-58-7.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1-METHYL-3-PHENYL-1H-[1,2,4]TRIAZOLE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-METHYL-3-PHENYL-1H-[1,2,4]TRIAZOLE(39696-58-7)
• EPA Substance Registry System: 1-METHYL-3-PHENYL-1H-[1,2,4]TRIAZOLE(39696-58-7)

Safety Data

• Hazardous Substances Data: 39696-58-7(Hazardous Substances Data)

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 
• 64-18-6 formic acid 
• 40994-01-2 N-methyl-benzamidrazone 
• 83274-32-2 N²-Methylbenzamidrazoniumiodid 
• 90145-13-4 N'-<α-bromobenzylidene>-N-methylhydrazinium bromide 
• 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 
• 83274-34-4 N²-tert-Butoxycarbonyl-N²-methylbenzamidrazoniumiodid 
• 41981-24-2 methyl benzenecarbimidothioate hydroiodide 

Relevant articles and documents

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

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