126800-02-0

Basic information

• Product Name: 1H-1,2,3-Triazole, 1-[(4-methylphenyl)methyl]-4-phenyl-
• CAS NO: 126800-02-0
• Molecular Formula: C16H15N3
• Molecular Weight: 249.315
• Mol File: 126800-02-0.mol
• Article Data: 120

Chemical Properties

• CAS DataBase Reference: 1H-1,2,3-Triazole, 1-[(4-methylphenyl)methyl]-4-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-1,2,3-Triazole, 1-[(4-methylphenyl)methyl]-4-phenyl-(126800-02-0)
• EPA Substance Registry System: 1H-1,2,3-Triazole, 1-[(4-methylphenyl)methyl]-4-phenyl-(126800-02-0)

Safety Data

• Hazardous Substances Data: 126800-02-0(Hazardous Substances Data)

Upstream product

• 17271-89-5 4-methylphenylmethylazide 
• 536-74-3 phenylacetylene 
• 104-82-5 4-Methylbenzyl chloride 
• 103-64-0 bromostyrene 
• 100-52-7 benzaldehyde 
• 5153-67-3 nitrostyrene 
• 104-81-4 4-Methylbenzyl bromide 
• 140-10-3 (E)-3-phenylacrylic acid 
• 70978-37-9 1-(azidomethyl)-4-methoxybenzene 

Downstream Products

• 1379671-49-4 1-(4-methylbenzyl)-4,5-diphenyl-1H-1,2,3-triazole 
• 1150635-10-1 1-(4-methoxyphenyl)-2-(4-phenyl-1H-1,2,3-triazole-1-yl)-1-ethanone 

Relevant articles and documents

Porphyrin-based mixed-valent Ag(i)/Ag(ii) and Cu(i)/Cu(ii) networks as efficient heterogeneous catalysts for the azide-alkyne "click" reaction and promising oxidation of ethylbenzene

By using a new porphyrin-based linker, two unusual mixed-valent Ag(i,ii)- and Cu(i,ii)-organic networks were synthesized. Most strikingly, 1 and 2 exhibit highly efficient catalytic activities for the azide-alkyne "click" reaction and oxidation of ethylbe

Construction of Stable Metal–Organic Framework Platforms Embedding N-Heterocyclic Carbene Metal Complexes for Selective Catalysis

We report a bottom-up approach to immobilize catalysts into MOFs, including copper halides and gold chloride in a predictable manner. Interestingly, the structures of MOFs bearing NHC metal complexes maintained a similar 4-fold interpenetrated cube. They

Resorcin[4]arene-based Cu(I) binuclear and mononuclear complexes as efficient catalysts for azide-alkyne cycloaddition reactions

In this study, three fascinating resorcin[4]arene-based Cu(I) complexes, named [CuCl (TPC4R)] (1), [CuBr (TPC4R)] (2), and [Cu2I2(TPC4R)] (3) were prepared by using a pyrimidine-functionalized resorcin[4]arene ligand (TPC4R). In 1 an

Dipolar HCP materials as alternatives to DMF solvent for azide-based synthesis

Hypercrosslinked polymers HCP-DMF and HCP-DMF-SO3H containing abundant and flexible DMF moieties were designed and synthesized. Benefitting from the solvation microenvironment provided by the pseudo-DMF moities, the polar HCPs manifested outstanding performances in the conversions of NaN3 to benzylic azides and 1,2,3-triazoles in EtOH (95%), respectively, avoiding the use of risky DMF and improving the separation processes of the products.