147795-56-0

Basic information

• Product Name: ethyl 2-(4-chlorophenyl)-2-cyanoacetate
• CAS NO: 147795-56-0
• Molecular Weight: 223.659
• Mol File: 147795-56-0.mol
• Article Data: 11

Chemical Properties

• CAS DataBase Reference: ethyl 2-(4-chlorophenyl)-2-cyanoacetate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl 2-(4-chlorophenyl)-2-cyanoacetate(147795-56-0)
• EPA Substance Registry System: ethyl 2-(4-chlorophenyl)-2-cyanoacetate(147795-56-0)

Safety Data

• Hazardous Substances Data: 147795-56-0(Hazardous Substances Data)

Upstream product

• 105-56-6 ethyl 2-cyanoacetate 
• 790-41-0 4-chlorobenzoic anhydride 
• 106-39-8 bromochlorobenzene 
• 86409-62-3 tricarbonyl(1,4-dichlorobenzene)chromium⁽⁰⁾ 
• 637-87-6 1-Chloro-4-iodobenzene 
• 105-58-8 Diethyl carbonate 
• 140-53-4 p-chlorobenzyl cyanide 
• 106-46-7 para-dichlorobenzene 

Downstream Products

• 1316673-16-1 (R)-ethyl 2-(4-chlorophenyl)-2-cyano-2-((S)-2,5-dioxo-1-phenylpyrrolidin-3-yl)acetate 
• 211697-03-9 diethyl 2,3-dicyano-2,3-di-(p-chlorophenyl)succinate 
• 139257-70-8 meso-diethyl 2,3-dicyano-2,3-di-(p-chlorophenyl)succinate 
• 838821-45-7 C₂₁H₂₈ClN₃O₆ 
• 3974-10-5 <4-Chlor-phenyl>-malonsaeure-amid 
• 802585-81-5 3-Chloro-2-(4-chloro-phenyl)-propylamine 
• 21463-50-3 1-chloro-4-(2-chloro-1-isothiocyanatomethyl-ethyl)-benzene 
• 21464-46-0 3-Amino-2-(4-chlor-phenyl)-propanol-⁽¹⁾ 

Relevant articles and documents

Phosphine-catalyzed regioselective Michael addition to allenoates

The first phosphine catalysed Michael addition of arylcyanoacetates to allenoates has been developed, and the β-selective products with a quaternary center were obtained in excellent yields. This unusual regioselectivity may open new opportunities to acce

Metal-free photochemical aromatic perfluoroalkylation of α-cyano arylacetates

We report here an operationally simple protocol for the direct aromatic perfluoroalkylation and trifluoromethylation of α-cyano arylacetates. This metal-free approach, which occurs at ambient temperature and under visible-light irradiation, is driven by t

Process for Preparing 2-Arylcarbonyl Compounds, 2-Aryl Esters and 2-Arylnitriles and their Heteroaromatic Analogues

Process for preparing compounds by cross-coupling of enolizable carbonyl compounds, nitriles or their analogues with substituted aryl or heteroaryl compounds in the presence of a Br?nsted base and of a catalyst or precatalyst containing a.) a transition m