1248337-32-7

Basic information

• Product Name: ethyl (Z)-3-((4-methoxyphenyl)amino)acrylate
• Synonyms: ethyl (Z)-3-((4-methoxyphenyl)amino)acrylate
• CAS NO: 1248337-32-7
• Molecular Weight: 221.256
• Mol File: 1248337-32-7.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: ethyl (Z)-3-((4-methoxyphenyl)amino)acrylate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl (Z)-3-((4-methoxyphenyl)amino)acrylate(1248337-32-7)
• EPA Substance Registry System: ethyl (Z)-3-((4-methoxyphenyl)amino)acrylate(1248337-32-7)

Safety Data

• Hazardous Substances Data: 1248337-32-7(Hazardous Substances Data)

Upstream product

• 104-94-9 4-methoxy-aniline 
• 623-47-2 propynoic acid ethyl ester 
• 34780-29-5 3-oxo-propionic acid ethyl ester 

Downstream Products

• 1236203-51-2 diethyl 4-(2-ethoxy-2-oxoethyl)-1-(4-methoxyphenyl)-1,4-dihydropyridine-3,5-dicarboxylate 
• 1248337-50-9 (R)-ethyl 1-(4-methoxyphenyl)-4-(4-nitrophenyl)-1,4-dihydropyridine-3-carboxylate 
• 1248337-36-1 (S)-ethyl 1-(4-methoxyphenyl)-4-(4-nitrophenyl)-1,4-dihydropyridine-3-carboxylate 
• 1256796-22-1 ethyl 1-(4-methoxyphenyl)-6-(4-nitrophenyl)-1,6-dihydropyridine-3-carboxylate 
• 1256796-21-0 ethyl 1-(4-methoxyphenyl)-4-(4-nitrophenyl)-1,4-dihydropyridine-3-carboxylate 

Relevant articles and documents

Green H 2 O-Promoted Solvent-Free Synthesis of Enaminocarbonyl Compounds with High Stereoselectivity from Electron-Deficient Terminal Alkynes

A green H 2 O-promoted solvent-free hydroamination of electron-deficient terminal alkynes with amines has been developed. All secondary amines, including aliphatic and aromatic amines, gave the corresponding (E)-enamines in good to excellent yi

Catalytic asymmetric synthesis of both enantiomers of 4-substituted 1,4-Dihydropyridines with the use of bifunctional Thiourea-Ammonium salts bearing different counterions

Organoammonium salts composed of a Bronsted acid and an anilinothiourea promoted the Michael addition of β-keto esters and α,β-unsaturated aldehydes in the presence of primary amines to give functionalized 1,4-dihydropyridines enantioselectively. With the