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Structure of 924-99-2
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Ethyl 3-(dimethylamino)acrylate features a conjugated enamine system that enhances reactivity in Michael additions and copolymerization. The electron-rich dimethylamino group stabilizes adjacent charge development, enabling efficient coupling under mild conditions. This acrylate derivative exhibits excellent solubility in common organic solvents and maintains stability during storage. It serves as a key building block for functional polymers and bioactive molecule synthesis.
Ethyl 3-(dimethylamino)acrylate serves as a versatile Michael acceptor and dienophile in conjugate addition and Diels–Alder reactions, enabling efficient construction of nitrogen-containing heterocycles. Its electron-rich enamine functionality enhances reactivity in nucleophilic additions while maintaining bench stability and ease of purification. The ester group permits further derivatization, making it a practical building block for synthetic intermediates in medicinal chemistry and materials science applications.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: