1314406-59-1

Basic information

• Product Name: 1-benzyl-4-(4-ethyl-phenyl)-1H-1,2,3-triazole
• Synonyms: 1-benzyl-4-(4-ethyl-phenyl)-1H-1,2,3-triazole
• CAS NO: 1314406-59-1
• Molecular Weight: 263.342
• Mol File: 1314406-59-1.mol
• Article Data: 25

Chemical Properties

• CAS DataBase Reference: 1-benzyl-4-(4-ethyl-phenyl)-1H-1,2,3-triazole(CAS DataBase Reference)
• NIST Chemistry Reference: 1-benzyl-4-(4-ethyl-phenyl)-1H-1,2,3-triazole(1314406-59-1)
• EPA Substance Registry System: 1-benzyl-4-(4-ethyl-phenyl)-1H-1,2,3-triazole(1314406-59-1)

Safety Data

• Hazardous Substances Data: 1314406-59-1(Hazardous Substances Data)

Upstream product

• 1431726-43-0 4-(4-ethylphenyl)-1-(methylsulfonyl)-1H-1,2,3-triazole 
• 100-39-0 benzyl bromide 
• 40307-11-7 1-ethyl-4-ethynylbenzene 
• 622-79-7 benzyl azide 
• 100-44-7 benzyl chloride 

Relevant articles and documents

Base-Induced Highly Regioselective Synthesis of N2-Substituted 1,2,3-Triazoles under Mild Conditions in Air

We developed a highly regioselective base-induced synthesis of N2-substituted 1,2,3-triazoles from N-sulfonyl-1,2,3-triazoles and alkyl bromides/alkyl iodides at room temperature. We propose an SN2-like mechanistic pathway to explain the high N2-regioselectivity. The protocol features a broad substrate scope and generates products in good to excellent yields (72–90%).

A new amido-phosphane as ligand for copper and silver complexes. Synthesis, characterization and catalytic application for azide-alkyne cycloaddition in glycerol

The new sterically hindered amido-phosphane 1,3,7-triaza-5-phosphabicyclo[3.3.1]nonane-3,7-diylbis(phenylmethanone), DBPTA (1), has been obtained via an open-cage double N-acylation of 1,3,5-triaza-7-phosphadamantane (PTA) using benzoic anhydride. DBPTA i

An Efficient Mesoporous Cu-Organic Nanorod for Friedl?nder Synthesis of Quinoline and Click Reactions

Within the green chemistry context, heterogeneous catalysis for the synthesis of N-heterocycles from renewable resources using non-precious metals has garnered great interest in terms of economic and environmental perspectives. Herein, we present a triazine functional hierarchical mesoporous organic polymer (HMOP) with nanorod morphology together with large BET surface area ～1218 m2 g?1, huge pore volumeγτ“;6 mL g?1 and dual micro/mesopore architectures. Subsequent Cu-coordination with nitrogen atoms of the HMOP provides a robust catalyst (Cu-HMOP) to accomplish multi-step cascade reactions for preparation of N-heterocycles by different routes. For instance, the Cu-HMOP efficiently catalyzes one-pot sequential multi-step oxidative dehydrogenative coupling of 2-aminobenzyl alcohol with diverse aromatic ketones to afford corresponding quinolines in excellent isolated yields (up to 97 %). Secondly, the present catalyst exhibits good aerobic oxidative dehydrogenation activity of amines to imines. Thirdly, for “click” reaction involving azides-alkynes, the Cu-HMOP produced quantitative yield for 1,4-disubstituted 1,2,3-triazole derivatives at room temperature using water as solvent. Verification of active metal leaching by a hot filtration test as well as reusability of the retrieved Cu-HMOP catalysts shows a consistent activity in the multi-component quinoline synthesis as model reaction.