63778-13-2

Basic information

• Product Name: 1H-1,2,3-Triazole, 1-[(2-chlorophenyl)methyl]-4-phenyl-
• CAS NO: 63778-13-2
• Molecular Formula: C15H12ClN3
• Molecular Weight: 269.733
• Mol File: 63778-13-2.mol
• Article Data: 32

Chemical Properties

• CAS DataBase Reference: 1H-1,2,3-Triazole, 1-[(2-chlorophenyl)methyl]-4-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-1,2,3-Triazole, 1-[(2-chlorophenyl)methyl]-4-phenyl-(63778-13-2)
• EPA Substance Registry System: 1H-1,2,3-Triazole, 1-[(2-chlorophenyl)methyl]-4-phenyl-(63778-13-2)

Safety Data

• Hazardous Substances Data: 63778-13-2(Hazardous Substances Data)

Upstream product

• 63777-70-8 2-chlorobenzylazide 
• 536-74-3 phenylacetylene 
• 611-19-8 1-chloro-2-(chloromethyl)benzene 
• 637-44-5 phenylpropyolic acid 
• 588-73-8 (Z)-β-bromostyrene 
• 611-17-6 1-bromomethyl-2-chlorobenzene 
• 17849-38-6 2-Chlorobenzyl alcohol 
• 109131-75-1 2-chloro-1-(4-methylbenzenesulfonyloxymethyl)benzene 
• 588-72-7 [(E)-2-bromoethenyl]benzene 

Relevant articles and documents

Highly efficient synthesis of silica-coated magnetic nanoparticles modified with iminodiacetic acid applied to synthesis of 1,2,3-triazoles

Great efforts have been made to discover new catalysts to facilitate synthesis of organic fine chemicals. In this research, a new silica-coated magnetic nanoparticles functionalized by iminodiacetic acid (Fe3O4@SiO2@IDA) w

Melamine-supported nickel oxide nanoparticles as a good alternative to conventional copper catalysts for the regioselective synthesis of triazole derivatives in water

Nickel oxide nanoparticles supported on melamine as a good alternative to conventional copper catalysts have been prepared and used for the regioselective synthesis of triazole derivatives in water. This catalyst can be reused several times without any si

Method for synthesizing P-1,4- substituted triazole 1, 2, 3- in alkynylic acid (by machine translation)

The method comprises the following steps: adding water to a reaction bottle; adding water to 1,4 - the 1, 2, 3 - reaction flask; adding water; extracting with ethyl acetate; extracting with 1.2 ethyl acetate; 1.0 adding ethyl acetate; 0.05 drying the ethy