1007597-65-0

Basic information

• Product Name: 1-methyl-3-(2-phenylethynyl)imidazolidin-2-one
• Synonyms: 1-methyl-3-(2-phenylethynyl)imidazolidin-2-one
• CAS NO: 1007597-65-0
• Molecular Weight: 200.24
• Mol File: 1007597-65-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1-methyl-3-(2-phenylethynyl)imidazolidin-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: 1-methyl-3-(2-phenylethynyl)imidazolidin-2-one(1007597-65-0)
• EPA Substance Registry System: 1-methyl-3-(2-phenylethynyl)imidazolidin-2-one(1007597-65-0)

Safety Data

• Hazardous Substances Data: 1007597-65-0(Hazardous Substances Data)

Upstream product

• 694-32-6 1-methyl-2-imidazolidone 
• 536-74-3 phenylacetylene 
• 637-44-5 phenylpropyolic acid 

Downstream Products

• 1228045-80-4 1-methyl-3-[3-(2-oxo-2-phenylethyl)-2-phenyl-3H-inden-1-yl]imidazolidin-2-one 
• 1228045-77-9 1-methyl-3-[1-(2-oxo-2-phenylethyl)-3-phenyl-1H-inden-2-yl]imidazolidin-2-one 
• 1228045-66-6 1-(1-hydroxy-3-phenyl-1H-inden-2-yl)-3-methylimidazolidin-2-one 
• 1356545-25-9 isobutyric acid (E)-1-(3-methyl-2-oxoimidazolidin-1-yl)-2-phenylvinyl ester 
• 1190789-25-3 1-[(E)-2-(3-chlorophenyl)-2-phenylvinyl]-3-methylimidazolidin-2-one 
• 1190789-20-8 1-[(E)-2,4-diphenylbut-1-en-3-ynyl]-3-methylimidazolidin-2-one 
• 1134172-54-5 3-methyl-1-[(Z)-2-phenylpropenyl]imidazolidin-2-one 

Relevant articles and documents

Cu-catalyzed oxidative amidation of propiolic acids under air via decarboxylative coupling

Figure presented A Cu-catalyzed aerobic oxidative amidation of propiolic acids via decarboxylation under air has been developed. Only carbon dioxide is produced as byproduct in this approach. The use of air as oxidant makes this method more useful and easy to handle.

Copper-catalyzed aerobic oxidative amidation of terminal alkynes: Efficient synthesis of ynamides

A copper-catalyzed method for the preparation of ynamides has been identified that proceeds via aerobic oxidative coupling of terminal alkynes with various nitrogen nucleophiles, including cyclic carbamates, amides and ureas, and N-alkyl-arylsulfonamides and indoles. Copyright