1417542-64-3

Basic information

• Product Name: N-methyl-2-phenoxy-N-((4-phenyl-1H-1,2,3-triazol-1-yl)methyl)acetamide
• Synonyms: N-methyl-2-phenoxy-N-((4-phenyl-1H-1,2,3-triazol-1-yl)methyl)acetamide
• CAS NO: 1417542-64-3
• Molecular Weight: 322.367
• Mol File: 1417542-64-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N-methyl-2-phenoxy-N-((4-phenyl-1H-1,2,3-triazol-1-yl)methyl)acetamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-methyl-2-phenoxy-N-((4-phenyl-1H-1,2,3-triazol-1-yl)methyl)acetamide(1417542-64-3)
• EPA Substance Registry System: N-methyl-2-phenoxy-N-((4-phenyl-1H-1,2,3-triazol-1-yl)methyl)acetamide(1417542-64-3)

Safety Data

• Hazardous Substances Data: 1417542-64-3(Hazardous Substances Data)

Upstream product

• 50-00-0 formaldehyd 
• 15422-25-0 N-methyl-2-phenoxyacetamide 
• 536-74-3 phenylacetylene 

Relevant articles and documents

Copper-catalyzed click synthesis of functionalized 1,2,3-triazoles with 3,4-dihydropyrimidinone or amide group via a one-pot four-component reaction

A Cu (I) generated in situ from Cu(OAc)2·H 2O/sodium ascorbate catalyzed one-pot multicomponent reaction for the synthesis of a series of N-functionalized 1,2,3-triazoles with 3,4-dihydropyrimidione from 3,4-dihydropyrimidiones, paraformaldehyde, sodium azide and alkynes is described. Remarkably N-functionalized 1,2,3-triazoles with amide were prepared by this method. This procedure eliminates the need to handle organic halides or organic azides, as they are generated in situ, making this already powerful click process even more user-friendly and safe.