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Structure of 15029-36-4
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2-Cyano-N-ethylacetamide features a dual functional group architecture: a nitrile moiety paired with an N-ethylamido linkage. This combination enables participation in nucleophilic addition reactions and facilitates integration into synthetic scaffolds requiring polar yet stable intermediates. The molecule exhibits robust bench stability under standard conditions, supporting reliable use in multistep transformations.
2-Cyano-N-ethylacetamide serves as a versatile building block in synthetic organic chemistry, enabling efficient access to nitrile-containing heterocycles and functionalized acetonitrile derivatives. Its dual functionality—cyano and amide groups—supports diverse transformations including hydrolysis, nucleophilic addition, and cyclization reactions. The molecule exhibits good bench stability and facilitates straightforward purification, making it well-suited for iterative synthesis workflows in medicinal chemistry and process development.
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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: