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Structure of 6629-04-5
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Ethyl (2-cyanoacetyl)carbamate features a cyanoacetyl scaffold that integrates seamlessly into heterocyclic synthesis. The electrophilic nitrile group enables efficient Michael additions, while the ethyl carbamate moiety offers stability and ease of manipulation under standard conditions. This compound serves as a key intermediate in the construction of nitrogen-containing ring systems.
Ethyl (2-cyanoacetyl)carbamate serves as a versatile building block in synthetic organic chemistry, enabling efficient access to cyano-substituted heterocycles and functionalized carbamates. Its dual reactivity—cyano group participation in Michael additions and cyclizations, and the carbamate moiety’s stability under basic conditions—facilitates straightforward incorporation into diverse scaffolds. Bench-stable and readily purified by column chromatography, it functions reliably in multistep syntheses of pharmaceutical intermediates and agrochemicals.
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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: