27888-23-9

Upstream product

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

Downstream Products

• 154198-90-0 (E)-3-p-anisyl-2-cyano-2-propenoyl azide 
• 81585-31-1 4-oxo-6-(4-methoxyphenyl)-2-thioxohexahydropyrimidine-5-carbonitrile 
• 183136-98-3 N-(3-p-anisyl-2-cyano-2-propenoyl)thiourea 
• 183136-99-4 N,N'-bis(3-p-anisyl-2-cyano-2-propenoyl)thiourea 
• 183137-06-6 N,N'-bis-(3-p-anisyl-2-cyano-2-propenoyl)phenylenediamine(o-) 
• 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 

Relevant academic research and scientific papers

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

Synthesis and transformations of derivatives and analogs of α-cyanocinnamic acid

A reaction of ethyl α-cyanoacetate with 5-arylfurfurals, furfural, and 4-methoxybenzaldehyde in alkaline water medium gives rise to 3-substituted 2-cyanoacrylic acids in high yield. The reaction of the corresponding acyl chlorides with diethylamine and an

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.