1235527-54-4

Basic information

• Product Name: 4-((4-phenyl-1H-1,2,3-triazol-4-yl)methyl)benzoic acid
• Synonyms: 4-((4-phenyl-1H-1,2,3-triazol-4-yl)methyl)benzoic acid
• CAS NO: 1235527-54-4
• Molecular Weight: 279.298
• Mol File: 1235527-54-4.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 4-((4-phenyl-1H-1,2,3-triazol-4-yl)methyl)benzoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 4-((4-phenyl-1H-1,2,3-triazol-4-yl)methyl)benzoic acid(1235527-54-4)
• EPA Substance Registry System: 4-((4-phenyl-1H-1,2,3-triazol-4-yl)methyl)benzoic acid(1235527-54-4)

Safety Data

• Hazardous Substances Data: 1235527-54-4(Hazardous Substances Data)

Upstream product

• 536-74-3 phenylacetylene 
• 6232-88-8 4-bromomethylbenzoic Acid 

Relevant articles and documents

Functionalized hypercrosslinked polymers with knitted N-heterocyclic carbene-copper complexes as efficient and recyclable catalysts for organic transformations

An N-heterocyclic carbene (NHC)-copper complex supported on hypercrosslinked polymers (HCPs) was successfully synthesized through a simple external cross-linking reaction. The structure and composition of the catalyst were characterized by scanning electr

Parallel solid-phase synthesis of diaryltriazoles

A series of substituted diaryltriazoles was prepared by a solid-phase-synthesis protocol using a modified Wang resin. The copper(I)-or ruthenium(II)-catalyzed 1,3-cycloaddition on the polymer bead allowed a rapid synthesis of the target compounds in a parallel fashion with in many cases good to excellent yields. Substituted diaryltriazoles resemble a molecular structure similar to established terphenyl-alpha-helix peptide mimics and have therefore the potential to act as selective inhibitors for protein-protein interactions.