107165-82-2

Basic information

• Product Name: Ethanone, 1-(4-chlorophenyl)-2-(2-imidazolidinylidene)-
• CAS NO: 107165-82-2
• Molecular Formula: C11H11ClN2O
• Molecular Weight: 222.674
• Mol File: 107165-82-2.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: Ethanone, 1-(4-chlorophenyl)-2-(2-imidazolidinylidene)-(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanone, 1-(4-chlorophenyl)-2-(2-imidazolidinylidene)-(107165-82-2)
• EPA Substance Registry System: Ethanone, 1-(4-chlorophenyl)-2-(2-imidazolidinylidene)-(107165-82-2)

Safety Data

• Hazardous Substances Data: 107165-82-2(Hazardous Substances Data)

Upstream product

• 107-15-3 ethylenediamine 
• 50850-04-9 1-(4-chlorophenyl)-3,3-dimercapto-2-propen-1-one 
• 4640-66-8 p-chlorobenzoylacetonitrile 
• 81471-33-2 3-(4-Chlorphenyl)-3-oxo-propionimidsauere-ethylester-hydrochlorid 
• 41467-26-9 1-(4-chlorophenyl)-3,3-bis(methylsulfanyl)-2-propen-1-one 

Downstream Products

• 118792-72-6 [7-(4-Chloro-benzoyl)-5-oxo-2,3,5,6-tetrahydro-1H-pyrrolo[1,2-a]imidazol-6-yl]-acetic acid 
• 138963-31-2 2-<(4-chlorobenzoyl)(2,4-dinitrophenyl)methylene>imidazolidine 
• 132111-57-0 3-(p-chlorobenzoyl)-5,6-dihydro-4H-imidazo-<1,2-c><1,2,3>triazole 
• 132111-45-6 1,5-bis(p-chlorophenyl)-4-(2-imidazolinyl)-1,2,3-triazole 
• 132111-53-6 1-(p-methoxyphenyl)-4-(2-imidazolinyl)-5-(p-chlorophenyl)-1,2,3-triazole 
• 112030-66-7 1-(4-Chloro-phenyl)-2-(4,5-dihydro-1H-imidazol-2-yl)-ethanone; hydrochloride 
• 115859-87-5 7-(4-chlorobenzoyl)-1,2,3,6-tetrahydro-5H-pyrrolo<1,2-a>imidazol-5-one 
• 126004-47-5 8-(4-chlorobenzoyl)-2,3,6,7-tetrahydroimidazo<1,2-a>pyridin-5(1H)-one 
• 107165-86-6 methyl-4-<(4-chlorobenzoyl)-2-imidazolidinylidene>-(E)-but-2-enoate 
• 1202699-16-8 2-[(4-chlorobenzoyl)(3,4-dihydroxy-5-methoxyphenyl)methylene]imidazolidine 
• 1202699-00-0 2-[(4-chlorobenzoyl)(4,5-dihydroxy-2-methylphenyl)methylene]imidazolidine 
• 1192054-05-9 C₁₅H₁₀ClF₃N₂O₂ 
• 1192054-10-6 C₁₅H₁₃ClN₂O₂ 
• 1146216-93-4 C₁₉H₁₀Cl₄N₄O 

Relevant articles and documents

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

The synthesis of fluoroheterocyclic ketene aminals

The synthesis of fluoroheterocyclic ketene aminals was investigated. Fluorobenzyl ketene dithioacetals 1c reacted with nitric acid in the presence of concentrated sulfuric acid to give compound 2c. 1 reacted with diamines to afford 3-4. C-fluorobenzylatio

Multicomponent Tether Catalysis Synthesis of Highly Functionalized 4-(Pyridin-2-ylmethyl)-2-aminopyrroles via Cascade Reaction Is Accompanied by Decarboxylation

A multicomponent tether catalysis protocol for the synthesis of 4-(pyridin-2-ylmethyl)-2-aminopyrroles (PMAPs) was constructed by simply refluxing a mixture of ethyl 2-(pyridin-2-yl)acetates 1 and various types of arylglyoxal monohydrates 2 and different heterocyclic ketene aminals 3 in EtOH solvent. Based on this reaction, a series of highly functionalized PMAPs were obtained through a novel cascade reaction accompanied by a decarboxylation mechanism. As a result, the pyridin-2-ylmethyl was successfully introduced in the target compounds, and a library of PMAPs were easily constructed using the cascade reaction described in this study. This protocol demonstrated that the most important feature was the decarboxylation reaction of the 2-(pyridin-2-yl)acetates 1, which can be used in the synthesis of pyridin-2-ylmethyl-substituted heterocycles, including pyrroles, pyridines, quinolones, and other heterocyclic compounds resembling those found in nature.