3533-10-6

Basic information

• Product Name: 3-(2-chlorophenyl)-2-cyanoprop-2-enamide
• CAS NO: 3533-10-6
• Molecular Formula: C₁₀H₇ClN₂O
• Molecular Weight: 206.6284
• Mol File: 3533-10-6.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 442.6°C at 760 mmHg
• Flash Point: 221.5°C
• Density: 1.351g/cm³
• Vapor Pressure: 4.94E-08mmHg at 25°C
• Refractive Index: 1.638
• CAS DataBase Reference: 3-(2-chlorophenyl)-2-cyanoprop-2-enamide(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(2-chlorophenyl)-2-cyanoprop-2-enamide(3533-10-6)
• EPA Substance Registry System: 3-(2-chlorophenyl)-2-cyanoprop-2-enamide(3533-10-6)

Safety Data

• Hazardous Substances Data: 3533-10-6(Hazardous Substances Data)

Upstream product

• 1352994-27-4 5-amino-3-(2-chlorophenyl)-2,3-dihydroisoxazole-4-carbonitrile 
• 2698-41-1 o-chlorobenzylidene malononitrile 
• 89-98-5 2-chloro-benzaldehyde 
• 109-77-3 malononitrile 
• 70380-66-4 2-chlorobenzaldehyde dimethyl acetal 
• 107-91-5 cyanoacetic acid amide 

Downstream Products

• 3695-90-7 E‐2‐cyano‐3‐(furan‐2‐yl)acrylamide 
• 6639-47-0 1,3,5-tris(p-tolyl)hexahydro-s-triazine 
• 74738-15-1 4-(2-chlorophenyl)-1H-pyrrole-3-carbonitrile 
• 1255086-54-4 2-amino-4-(2-chlorophenyl)-1-(4-chlorophenyl)-7,7-dimethyl-1,4,5,6,7,8-hexahydroquinolin-5-one 

Relevant articles and documents

Phenyl pyrrole compound and application thereof in bactericidal activity

The invention provides a novel phenyl pyrrole compound, and the phenyl pyrrole compound shows good bactericidal activity and can be used for preparing a broad-spectrum plant bactericide. In addition,the synthesis route is simple, the operation is convenient, the synthesis cost is reduced, and ecological environment pollution to soil, surface water, underground water and the like is avoided.

Cascade Synthesis of 2-Cyanoacrylamides through Deacetalization and/or Knoevenagel Condensation followed by Selective Monohydration of Acetals and Aldehydes over Solid Acid Ferrites

A new protocol of cascade synthesis for biologically active 2-cyanoacrylamides (1) was developed. The reaction proceeds over a novel magnetically retrievable solid-acid composite of iron oxide, poly(vinylpyrrolidone) and phosphotungstic acid (Fe3O4/PVP–PWA) in AcOH–H2O medium under reflux conditions. This transformation is facilitated through single-site Br?nsted acid catalyzed cascade reactions involving deacetalization and/or Knoevenagel condensation followed by selective monohydration of nitriles starting from acetals (5) and aldehydes (2) with malononitrile (3). A series of aldehydes, dimethyl and diethyl acetals, along with some heterocyclic aldehydes were successfully transformed to 2-cyanoacrylamides with >95 % yields. TEM images confirmed the coating of the PVP over nanosized Fe3O4. Stereoselective monohydration of 2-benzylidenemalononitriles (4) to E isomers was demonstrated by NOESY experiments. The catalyst could be efficiently recycled seven times on employment of both acetals and aldehydes as substrates, as a result of its magnetic nature.

Synthesis of functionalized 2,3-dihydroisoxazoles by domino reactions in water and unexpected ring-opening reactions of 2,3-dihydroisoxazoles

α,α-Dicyanoolefins react with hydroxylamine to afford 2,3-dihydroisoxazoles (2,3-dihydroisoxazoles can be easily isolated by filtration) in excellent yields under mild and environmentally benign conditions. A one-pot reaction in tandem with an unexpected ring-opening of 2,3-dihydroisoxazoles has been developed as well.