689257-75-8

Usage

Uses

Used in Polymer Chemistry:
(E)-N-methoxy-N-methyl-3-(3,4-dimethoxyphenyl)-acrylamide is used as a monomer in polymer chemistry for the synthesis of polymers with specific properties. The acrylamide group in the compound allows for polymerization reactions, which can lead to the creation of polymers with tailored characteristics for various applications.
Used in Pharmaceutical Applications:
In the pharmaceutical industry, (E)-N-methoxy-N-methyl-3-(3,4-dimethoxyphenyl)-acrylamide is used as a potential candidate for drug development. The presence of methoxy and dimethoxyphenyl groups, which are often found in biologically active molecules, suggests that (E)-N-methoxy-N-methyl-3-(3,4-dimethoxyphenyl)-acrylamide may have pharmacological or biological activities. Further research is needed to explore its potential as a therapeutic agent.
Used in Biological Research:
(E)-N-methoxy-N-methyl-3-(3,4-dimethoxyphenyl)-acrylamide may also be utilized in biological research as a tool to study the interactions of various cellular components. (E)-N-methoxy-N-methyl-3-(3,4-dimethoxyphenyl)-acrylamide's structure could allow it to serve as a probe or modifier for specific biological targets, providing insights into cellular processes and potential therapeutic strategies.

Upstream product

• 6638-79-5 N,O-dimethylhydroxylamine*hydrochloride 
• 39856-08-1 3,4-dimethoxy-cinnamoyl chloride 
• 2316-26-9 3,4-dimethoxycinnamic acid 
• 14737-89-4 3,4-dimethoxy-trans-cinnamic acid 

Downstream Products

• 436145-75-4 (4R,9aS)-4-(3,4-dimethoxyphenyl)octahydro-2H-quinolizin-2-one 
• 875325-82-9 ethyl [2-(3,4-dimethoxyphenyl)cyclopropyl]acetate 

Relevant academic research and scientific papers

Double asymmetric intramolecular aza-Michael reaction: a convenient strategy for the synthesis of quinolizidine alkaloids

A new methodology to access the quinolizidine skeleton in an asymmetric fashion was devised. It involves two consecutive intramolecular aza-Michael reactions of sulfinyl amines bearing a bis-enone moiety, in turn generated by a monodirectional cross metat

Catalytic formal homo-Nazarov cyclization

The first catalytic method for the cyclization of vinyl-cyclopropyl ketones (formal homo-Nazarov reaction) is reported. Starting from activated cyclopropanes, heterocyclic, and carbocyclic compounds were obtained under mild conditions using Bronsted acid catalysts. Preliminary investigation of the reaction mechanism indicated a stepwise process.

Discovery of +(2-{4-[2-(5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)ethoxy]phenyl}-cyclopropyl)acetic acid as potent and selective αvβ3 inhibitor: Design, synthesis, and optimization

The integrin αvβ3 is expressed in a number of cell types and is thought to play a major role in several pathological conditions. Various small molecules that inhibit the integrin have been shown to suppress tumor growth and retinal a

Cycloalkyl alkanoic acids as integrin receptor antagonists derivatives

The present invention relates to a class of compounds represented by the Formula I or a pharmaceutically acceptable salt thereof, pharmaceutical compositions comprising compounds of the Formula I, and methods of selectively inhibiting or antagonizing the αvβ3 and/or αvβ5 integrin.