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Structure of 34916-10-4
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4-Cyanocyclohexanone features a conjugated nitrile group positioned para to a ketone on a cyclohexanone ring, enabling dual reactivity in synthetic transformations. This electron-deficient scaffold integrates readily into heterocyclic systems and serves as a key intermediate in the synthesis of nitrogen-containing pharmaceuticals and bioactive molecules under standard conditions.
4-Cyanocyclohexanone serves as a versatile building block in synthetic organic chemistry, enabling efficient access to nitrogen-containing heterocycles and functionalized cyclohexane scaffolds. Its conjugated enone system facilitates Michael additions, nucleophilic cyclizations, and transition-metal-catalyzed transformations. The nitrile group provides orthogonal reactivity for hydrolysis, reduction, or cyclization, supporting downstream derivatization in medicinal chemistry and process development. Bench-stable and readily purified by distillation or crystallization, it functions reliably in multi-step syntheses.
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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: