37389-84-7

Basic information

• Product Name: ethyl 2-cyano-3-(3,4-dimethoxyphenyl)propanoate
• Synonyms: ethyl 2-cyano-3-(3,4-dimethoxyphenyl)propanoate
• CAS NO: 37389-84-7
• Molecular Weight: 263.293
• Mol File: 37389-84-7.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: ethyl 2-cyano-3-(3,4-dimethoxyphenyl)propanoate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl 2-cyano-3-(3,4-dimethoxyphenyl)propanoate(37389-84-7)
• EPA Substance Registry System: ethyl 2-cyano-3-(3,4-dimethoxyphenyl)propanoate(37389-84-7)

Safety Data

• Hazardous Substances Data: 37389-84-7(Hazardous Substances Data)

Upstream product

• 2286-55-7 ethyl α-cyano-β-(3,4-dimethoxyphenyl)acrylate 
• 21852-32-4 4-bromomethyl-1,2-dimethoxybenzene 
• 372-09-8 cyanoacetic acid 

Downstream Products

• 65708-36-3 α-Carbethoxy-α-diethoxymethyl-β-[3,4-dimethoxyphenyl]propionitrile 
• 1196886-23-3 ethyl 2-(2-amino-5-nitro-6-oxo-1,6-dihydropyrimidin-4-yl)-2-cyano-3-(3,4-dimethoxyphenyl)propanoate 
• 1196886-25-5 2-(2-amino-5-nitro-6-oxo-1,6-dihydropyrimidin-4-yl)-3-(3,4-dimethoxyphenyl)propanenitrile 
• 1196886-27-7 7-(3,4-dimethoxybenzyl)-2-amino-3H-pyrrolo[3,2-d]pyrimidin-4(5H)-one 
• 1196881-88-5 7-(3,4-dimethoxybenzyl)-4-chloro-5H-pyrrolo[3,2-d]pyrimidin-2-amine 
• 1196881-90-9 7-(3,4-dimethoxybenzyl)-4-chloro-5-(4-methylpentyl)-5H-pyrrolo[3,2-d]pyrimidin-2-amine 
• 55502-61-9 2-cyano-3-(3,4-dimethoxyphenyl)propionic acid 

Relevant articles and documents

Asymmetric Reaction of p-Quinone Diimide: Organocatalyzed Michael Addition of α-Cyanoacetates

Hitherto unknown catalytic enantioselective transformation of p-quinone diimides is achieved using chiral bifunctional organic molecules. Bifunctional thiourea compounds catalyze the Michael addition of cyanoacetates with excellent yields and enantioselec

3-Butyl-1-methylimidazolinium borohydride ([bmim][BH4])-a novel reducing agent for the selective reduction of carbon-carbon double bonds in activated conjugated alkenes

A novel ionic reducing reagent, 3-butyl-1-methylimidazolium borohydride ([bmim][BH4]), was synthesized and successfully used for the selective reduction of carbon-carbon double bonds in conjugated alkenes as well as the α,β-carbon-carbon double bonds in highly activated α,β,γ,δ-unsaturated alkenes. The reagent can be regenerated and reused several times without losing its activity.