27888-23-9

Basic information

• Product Name: (E)-3-p-anisyl-2-cyano-2-propenoyl chloride
• Synonyms: (E)-3-p-anisyl-2-cyano-2-propenoyl chloride
• CAS NO: 27888-23-9
• Molecular Weight: 221.643
• Mol File: 27888-23-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (E)-3-p-anisyl-2-cyano-2-propenoyl chloride(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-3-p-anisyl-2-cyano-2-propenoyl chloride(27888-23-9)
• EPA Substance Registry System: (E)-3-p-anisyl-2-cyano-2-propenoyl chloride(27888-23-9)

Safety Data

• Hazardous Substances Data: 27888-23-9(Hazardous Substances Data)

Upstream product

• 14378-08-6 (E)-2-cyano-3-(4-methoxyphenyl)acrylic acid 
• 123-11-5 4-methoxy-benzaldehyde 
• 79-37-8 oxalyl dichloride 
• 135-02-4 ortho-anisaldehyde 

Downstream Products

• 183136-99-4 N,N'-bis(3-p-anisyl-2-cyano-2-propenoyl)thiourea 
• 23795-68-8 2-Cyan-3-<4-methoxy-phenyl>-N,N-diaethyl-acrylsaeureamid 
• 5349-42-8 (5Z)-5-(4-methoxybenzylidene)imidazolidine-2,4-dione 
• 154199-16-3 (Z)-2-Methoxycarbonylamino-3-(4-methoxy-phenyl)-acrylimidic acid ethyl ester 
• 154198-95-5 [(E)-1-Cyano-2-(4-methoxy-phenyl)-vinyl]-carbamic acid methyl ester 
• 154199-10-7 [1-Cyano-2-(4-methoxy-phenyl)-ethyl]-carbamic acid tert-butyl ester 
• 154199-09-4 2-Cyano-3-(4-methoxy-phenyl)-propionyl azide 
• 154199-02-7 [(E)-1-Cyano-2-(4-methoxy-phenyl)-vinyl]-carbamic acid ethyl ester 
• 154199-20-9 [(E)-1-Cyano-2-(4-methoxy-phenyl)-vinyl]-urea 
• 154198-92-2 (E)-2-Isocyanato-3-(4-methoxy-phenyl)-acrylonitrile 

Relevant articles and documents

Synthesis and biological evaluation of bifendate derivatives bearing acrylamide moiety as novel antioxidant agents

Oxidative stress plays a significant role in the pathogenesis of various human diseases. In this study, a series of bifendate derivatives bearing acrylamide moiety were synthesized and evaluated as anti-oxidant agents. Biological evaluation indicated that

α-Isocyanatoacrylonitriles from alkylidene- or arylidenecyanoacetic acids; synthesis and reactions

The Curtius reaction converts alkylidene- or arylidenecyanoacetic acids to α-isocyanatoacrylonitriles in a stereospecific way. These versatile intermediates allow an easy access to arylacetic acids and various amino acid derivatives, as well as β-lactams or 2-azabutadienes.