64944-80-5

Basic information

• Product Name: Ethanone, 2-(2-imidazolidinylidene)-1-phenyl-
• Synonyms: HMS1736C06;2-(imidazolidin-2-ylidene)-1-phenyl-ethanone;2-(imidazolidin-2-ylidene)-1-phenylethan-1-one;2-(2-oxo-2-phenylethylidene)imidazolidine;HMS2788G08;2-(benzoylmethylene)-imidazolidine
• CAS NO: 64944-80-5
• Molecular Formula: C11H12N2O
• Molecular Weight: 188.229
• Mol File: 64944-80-5.mol
• Article Data: 13

Chemical Properties

• CAS DataBase Reference: Ethanone, 2-(2-imidazolidinylidene)-1-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanone, 2-(2-imidazolidinylidene)-1-phenyl-(64944-80-5)
• EPA Substance Registry System: Ethanone, 2-(2-imidazolidinylidene)-1-phenyl-(64944-80-5)

Safety Data

• Hazardous Substances Data: 64944-80-5(Hazardous Substances Data)

Upstream product

• 13636-88-9 3,3-bis(methylthio)-1-phenylprop-2-en-1-one 
• 107-15-3 ethylenediamine 
• 81471-31-0 3-oxo-3-phenyl-propionimidic acid ethyl ester; hydrochloride 
• 70-11-1 α-bromoacetophenone 
• 37510-42-2 3,3-bis(ethylthio)-1-phenylprop-2-en-1-one 
• 100-42-5 styrene 
• 887144-94-7 Togni's reagent II 
• 614-16-4 Benzoylacetonitrile 
• 32188-99-1 2-phenacylthioimidazoline 

Downstream Products

• 118792-71-5 (7-Benzoyl-5-oxo-2,3,5,6-tetrahydro-1H-pyrrolo[1,2-a]imidazol-6-yl)-acetic acid 
• 138963-28-7 2-imidazolidine 
• 132111-40-1 1-(p-nitrophenyl)-4-(2-imidazolinyl)-5-phenyl-1,2,3-triazole 
• 115859-85-3 7-benzoyl-1,2,3,6-tetrahydro-5H-pyrrolo<1,2-a>imidazol-5-one 
• 115859-73-9 ethyl 3-benzoyl-3-(2-imidazolidinylidene)propionate 
• 136271-12-0 2-Imidazolidin-2-ylidene-2-(2-nitro-phenylazo)-1-phenyl-ethanone 
• 107165-89-9 8-Benzoyl-2,3-dihydro-1H-imidazo<1,2-a>pyridin-5(8H)-one 
• 150301-54-5 2-(1-benzoyl-3-ethoxycarbonylprop-2-enylidene)-2,3,4,5-tetrahydroimidazole 
• 164024-91-3 2-(benzoylmethylene)-1-benzylimidazolidine 

Relevant articles and documents

Direct Access to α-Oxoketene Aminals via Copper-Catalyzed Formal Oxyaminalization of Alkenes under Mild Conditions

A copper-catalyzed four-component formal oxyaminalization of alkenes with Togni's reagent and amines using molecular oxygen as both the oxidant and oxygen source has been developed for the first time, offering a straightforward and efficient method for the synthesis of a range of structurally diverse α-oxoketene aminals. The use of cheap copper catalyst and readily available substrates, excellent functional group tolerance, broad substrate scope, mild conditions, and simple procedure are the attractive features of the strategy.

Synthesis of Partially Reduced Imidazo[1,2- a ]pyridines through an Unprecedented Base-Mediated (4+2) Cyclization

A water-mediated regioselective synthesis of 6,7-diaryl-5-oxo-2,3,5,6-tetrahydroimidazo[1,2-a]pyridine-6-carbonitriles was performed by the reaction of 2-[1-cyano-2,2-bis(methylsulfanyl)vinyl]benzonitrile with 1-aryl-2-(imidazolidin-2-ylidene)ethanones un

Three-component synthesis of indanone-fused spirooxindole derivatives

A simple, straightforward and versatile multicomponent protocol for the synthesis of indanone-fused spirooxindole derivatives has been developed. The strategy involves the one-pot three-component reaction of heterocyclic ketene aminals, 1H-indene-1,3(2H)-