126800-00-8

Basic information

• Product Name: 1H-1,2,3-Triazole, 1-[(4-methoxyphenyl)methyl]-4-phenyl-
• CAS NO: 126800-00-8
• Molecular Formula: C16H15N3O
• Molecular Weight: 265.315
• Mol File: 126800-00-8.mol
• Article Data: 68

Chemical Properties

• CAS DataBase Reference: 1H-1,2,3-Triazole, 1-[(4-methoxyphenyl)methyl]-4-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-1,2,3-Triazole, 1-[(4-methoxyphenyl)methyl]-4-phenyl-(126800-00-8)
• EPA Substance Registry System: 1H-1,2,3-Triazole, 1-[(4-methoxyphenyl)methyl]-4-phenyl-(126800-00-8)

Safety Data

• Hazardous Substances Data: 126800-00-8(Hazardous Substances Data)

Upstream product

• 2393-23-9 4-methoxy-benzylamine 
• 2746-25-0 p-Methoxybenzyl bromide 
• 536-74-3 phenylacetylene 
• 70978-37-9 1-(azidomethyl)-4-methoxybenzene 
• 2170-06-1 1-Phenyl-2-(trimethylsilyl)acetylene 
• 140-10-3 (E)-3-phenylacrylic acid 
• 75-52-5 nitromethane 
• 100-52-7 benzaldehyde 
• 637-44-5 phenylpropyolic acid 
• 2101-87-3 p-methoxy-phenylazide 
• 103-64-0 bromostyrene 
• 588-72-7 [(E)-2-bromoethenyl]benzene 
• 588-73-8 (Z)-β-bromostyrene 
• 932-88-7 1-iodo-2-phenylethyne 

Downstream Products

• 1111662-33-9 1-(4-methoxybenzyl)-4-phenyl-5-p-tolyl-1H-1,2,3-triazole 

Relevant articles and documents

Discrete Benzotriazole-Copper(II) Complexes in Chelated and Non-Chelated Coordination Modes: Structural Analysis and Catalytic Application in Click and A3 Coupling Reactions

Two copper(II) complexes with benzotriazole-based ligands having pyridyl and quinolinyl arms were synthesized in good yields and characterized fully via spectroscopic and crystallographic techniques. The crystal structures of the complexes revealed differ

A novel route to 1,4-disubstituted-1,2,3-triazoles through metal-free decarboxylative azide-alkene cycloaddition

A collection of 1,4-disubstituted 1,2,3-triazoles was achieved by decarboxylative [3 + 2] cycloaddition of organic azides and cinnamic acids. Metal-free condition, high regioselectivity and easy accessibility of starting materials are the salient attributes of this protocol.

Multi-component reaction for the preparation of 1,5-disubstituted 1,2,3-triazoles by in-situ generation of azides and nickel-catalyzed azide-alkyne cycloaddition

An efficient one-pot procedure combining bromide conversion into azide followed by NiAAC for the preparation of 1,5-disubstituted 1,2,3-triazoles has been developed. This procedure prevents the use of isolated azides, which are insufficiently commercially