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Ethyl 3-(N,N-dimethylamino)acrylate CAS:924-99-2;1117-37-9

Ethyl 3-(N,N-dimethylamino)acrylate is an important organic compound characterized by the presence of an acrylate moiety and a N,N-dimethylamino group. With the chemical formula C10H17N O2, this compound exhibits unique properties due to its functional groups, making it valuable in various applications, particularly in polymer chemistry and medicinal chemistry. Its reactivity allows for participation in several chemical transformations, which are essential for synthesizing polymers and developing pharmaceutical agents. Ethyl 3-(N,N-dimethylamino)acrylate is often employed as a monomer in the production of coatings, adhesives, and other materials.


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Application and Effect:

Ethyl 3-(N,N-dimethylamino)acrylate is a clear, colorless liquid that is soluble in many organic solvents. The structure features an ethyl ester group attached to a conjugated double bond system with a dimethylamino substituent. This configuration endows the compound with a level of reactivity conducive to Michael additions and polymerization reactions. One of the primary applications of this compound lies in polymer chemistry, where it serves as a crucial monomer for synthesizing various copolymers through radical polymerization techniques. The incorporation of N,N-dimethylamino functionality provides enhanced solubility and facilitates ionic interactions, leading to improved performance characteristics in the resultant materials. As such, it is widely used in formulating coatings, adhesives, and sealants with tailored properties, such as adhesion, flexibility, and durability. In medicinal chemistry, ethyl 3-(N,N-dimethylamino)acrylate has garnered attention for its potential use in drug development. The N,N-dimethylamino group can serve as a site for further functionalization, enabling the design of new pharmaceutical compounds with specific biological activities. Research indicates that derivatives of this compound may exhibit properties beneficial for treating various conditions, highlighting its significance in therapeutic innovation. Furthermore, the compound's reactivity also allows for applications in photoresponsive materials, where it can be utilized in the production of light-activated systems. These systems have potential applications in drug delivery, smart coatings, and other advanced material technologies. Despite its numerous applications, safety and handling considerations must be observed when working with ethyl 3-(N,N-dimethylamino)acrylate. Proper laboratory practices should be employed to minimize exposure, as the compound can irritate the skin and eyes. In summary, ethyl 3-(N,N-dimethylamino)acrylate represents a versatile building block in both industrial and research contexts. Its functional capabilities enable a wide range of applications across diverse fields, from advanced materials to pharmaceuticals, underscoring its importance in contemporary organic chemistry and material science.

Product Sample:

L-Arginine1
L-Arginine2

Product Packing:

L-Arginin3

Additional Information:

Composition C7H13NO2
Assay 99%
Appearance white powder
CAS No.  924-99-2;1117-37-9
Packing Small and bulk
Shelf Life 2 years
Storage Store in cool and dry area
Certification ISO.

 


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