22056-04-8

Basic information

• Product Name: 2-[(4-chlorophenyl)hydroxymethyl]acrylonitrile
• Synonyms: 2-[(4-chlorophenyl)hydroxymethyl]acrylonitrile
• CAS NO: 22056-04-8
• Molecular Weight: 193.633
• Mol File: 22056-04-8.mol
• Article Data: 37

Chemical Properties

• CAS DataBase Reference: 2-[(4-chlorophenyl)hydroxymethyl]acrylonitrile(CAS DataBase Reference)
• NIST Chemistry Reference: 2-[(4-chlorophenyl)hydroxymethyl]acrylonitrile(22056-04-8)
• EPA Substance Registry System: 2-[(4-chlorophenyl)hydroxymethyl]acrylonitrile(22056-04-8)

Safety Data

• Hazardous Substances Data: 22056-04-8(Hazardous Substances Data)

Upstream product

• 104-88-1 4-chlorobenzaldehyde 
• 107-13-1 acrylonitrile 
• 1156004-08-8 2-(butylselanylmethyl)-3-(4-chlorophenyl)-3-hydroxypropanenitrile 
• 109-72-8 n-butyllithium 

Downstream Products

• 131469-64-2 2-(4-Chloro-benzoyl)-oxirane-2-carbonitrile 
• 172658-58-1 (E)-3-(4-Chloro-phenyl)-2-hydroxymethyl-acrylonitrile 
• 139413-83-5 (E)-2-(bromomethyl)-3-(4-chlorophenyl)acrylonitrile 
• 139413-84-6 (Z)-2-Bromomethyl-3-(4-chloro-phenyl)-acrylonitrile 
• 940-35-2 2-Methyl-3-(4-chlor-phenyl)-acrylnitril 
• 852287-74-2 3-(4-chloro-phenyl)-2-[(4-fluoro-benzylamino)-methyl]-3-hydroxy-propionitrile 
• 104-88-1 4-chlorobenzaldehyde 
• 852287-81-1 2-aminomethyl-3-benzylamino-1-(4-chloro-phenyl)-propan-1-ol 
• 852287-86-6 2-aminomethyl-1-(4-chloro-phenyl)-3-(4-fluoro-benzylamino)-propan-1-ol 
• 164208-54-2 Acetic acid 1-(4-chloro-phenyl)-2-cyano-allyl ester 

Relevant articles and documents

Iodine-catalyzed thioallylation of indoles using Bunte salts prepared from Baylis-Hillman bromides

Metal-free iodine-catalyzed regioselective thioallylation of indoles has been accomplished at room temperature using Bunte salts prepared from Baylis-Hillman bromides. The resulting multi-functional C3 thioallylated indoles exhibit ample structural divers

A one-pot three-step multicomponent synthesis of functionalized allyl dithiocarbamates using Baylis–Hillman reaction

A one-pot, pseudo five-component, highly diastereoselective, and mild procedure for the synthesis of functionalized allyl dithiocarbamates is developed. The Baylis–Hillman (BH) reaction of aromatic (heteroaromatic) aldehydes and activated alkenes using DA

Efficient synthesis of N-allylated 2-nitroiminoimidazolidine analogues from Baylis–Hillman bromides

Various Baylis–Hillman–derived new N-allylated 2-nitroiminoimidazolidine analogs were efficiently prepared using potassium carbonate as base. Simple workup procedure, excellent yields, and mild reaction conditions are the salient features of this method. All the synthesized compounds are screened for their larvicidal activity on fourth instar mosquito larvae, Culex quinquefasciatus.