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Structure of 4640-66-8
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4-Chlorophenacylcyanide features a reactive α-cyanocarbonyl moiety flanked by a para-chlorophenyl group, enabling efficient conjugation in synthetic transformations. This bench-stable reagent integrates readily into Michael addition cascades and nucleophilic substitution protocols under standard conditions.
4-Chlorophenacylcyanide serves as a versatile building block in synthetic organic chemistry, enabling efficient construction of heterocyclic scaffolds through nucleophilic addition and cyclization reactions. Its benzylic cyanide functionality exhibits high reactivity with amines and thiols, facilitating the synthesis of substituted pyridines, quinolines, and other nitrogen-containing heterocycles. The molecule’s bench-stable nature and compatibility with diverse functional groups make it well-suited for multi-step syntheses in medicinal chemistry and process development workflows.
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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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362-P405-P501
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Lot numbers can be found on the outside label of a product: