1240979-09-2

Basic information

• Product Name: 2,2-dimethyl-N-(3-phenylprop-2-yn-1-yl)propanamide
• Synonyms: 2,2-dimethyl-N-(3-phenylprop-2-yn-1-yl)propanamide
• CAS NO: 1240979-09-2
• Molecular Weight: 215.295
• Mol File: 1240979-09-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2,2-dimethyl-N-(3-phenylprop-2-yn-1-yl)propanamide(CAS DataBase Reference)
• NIST Chemistry Reference: 2,2-dimethyl-N-(3-phenylprop-2-yn-1-yl)propanamide(1240979-09-2)
• EPA Substance Registry System: 2,2-dimethyl-N-(3-phenylprop-2-yn-1-yl)propanamide(1240979-09-2)

Safety Data

• Hazardous Substances Data: 1240979-09-2(Hazardous Substances Data)

Upstream product

• 3282-30-2 pivaloyl chloride 
• 591-50-4 iodobenzene 
• 178320-73-5 2,2-dimethyl-N-(prop-2-ynyl)propionamide 

Downstream Products

• 29266-27-1 2-(tert-butyl)-5,6-diphenyl-5,6-dihydro-4H-1,3-oxazine 
• 1333470-73-7 (5Z)-5-benzylidene-2-tert-butyl-4,5-dihydro-1,3-oxazole 

Relevant articles and documents

Utilization of Copper-Catalyzed Carboarylation-Ring Closure for the Synthesis of New Oxazoline Derivatives

A copper-catalyzed carboarylation-ring-closure strategy was used for the modular synthesis of oxazolines via the reaction of 1-aryl- and 1-alkylpropargylamides and diaryliodonium salts. The novel approach enables the efficient, modular synthesis of oxazol

Gold-catalyzed cyclization of nonterminal propargylic amides to substituted alkylideneoxazolines and-oxazines

The substrate scope of the gold-catalyzed cyclization of nonterminal propargylic amides to oxazolines and oxazines was investigated. Sixteen alkyl-substituted and 35 aryl-substited substrates were prepared by a very variable route from trimethylsilyl-(TMS