68301-12-2

Basic information

• Product Name: 1H-1,2,4-Triazole, 1,3-dimethyl-5-phenyl-
• CAS NO: 68301-12-2
• Molecular Formula: C10H11N3
• Molecular Weight: 173.217
• Mol File: 68301-12-2.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 1H-1,2,4-Triazole, 1,3-dimethyl-5-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-1,2,4-Triazole, 1,3-dimethyl-5-phenyl-(68301-12-2)
• EPA Substance Registry System: 1H-1,2,4-Triazole, 1,3-dimethyl-5-phenyl-(68301-12-2)

Safety Data

• Hazardous Substances Data: 68301-12-2(Hazardous Substances Data)

Upstream product

• 302-15-8 methylhydrazine sulfuric acid 
• 87277-54-1 N-Benzoylacetimidsaeure-ethylester 
• 1575-95-7 N-acetylbenzamide 
• 84044-62-2 C₁₁H₁₅N₃*HI 
• 95643-04-2 C₁₀H₁₃N₃*HI 
• 41981-24-2 methyl benzenecarbimidothioate hydroiodide 
• 36787-47-0 N²-methylbenzamidrazonium iodide 
• 87277-54-1 ethyl N-benzoylacetimidate 
• 60-34-4 methylhydrazine 
• 95642-89-0 1,3,3-Trimethyl-5-phenyl-2,3-dihydro-1H-[1,2,4]triazole 
• 95642-88-9 1,3-Dimethyl-5-phenyl-2,3-dihydro-1H-[1,2,4]triazole 
• 186581-53-3 diazomethane 
• 3213-91-0 3-phenyl-5-methyl-<1.2.4>triazole 

Relevant articles and documents

Cationic Iridium Complexes with 5-Phenyl-1 H-1,2,4-triazole Type Cyclometalating Ligands: Toward Blue-Shifted Emission

Four cationic iridium complexes with 5-phenyl-1H-1,2,4-triazole (phtz) type cyclometalating ligands (C^N) and different ancillary ligands (N^N), namely, [Ir(dphtz)2(bpy)]PF6 (1), [Ir(dphtz)2(pzpy)]PF6 (2), [Ir(M

SYNTHESIS AND STRUCTURE OF 1-METHYL-2,3-DIHYDRO-1,2,4-TRIAZOLIUM SALTS AND THEIR FREE BASES

1-Methyl-2,3-dihydro-1,2,4-triazolium iodides can be obtained by reacting methylhydrazones with S-methylthioamide hydriodides, by condensing 2-methylamidrazone hydriodides with aldehydes and ketones, or by reacting methyl iodide with 1-alkylidene(or arylidene)benzamidrazones.In solutions these salts are capable of undergoing tautomerism to 1-alkylidene(or arylidene)-2-methylamidrazone hydriodides.The influence of the structural factors on the position of the tautomeric equilibrium has been studied.The free bases obtained by neutralization of the respective salts by an alkali metal hydroxides are heretofore underscribed 1-alkylidene(or a rylidene)-2-methylhydrazidoimines or 4-triazolines, depending on their structure.Under the action of oxygen, these compounds are readily oxidized to substituted 1-methyl-1,2,4-triazoles with heating.