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Structure of 487-51-4
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Ethyl 2-methyl-4-oxocyclohex-2-enecarboxylate features a conjugated enone system flanked by a methyl substituent and ester functionality, enabling direct participation in Diels-Alder reactions and Michael additions. This bicyclic scaffold delivers structural rigidity and regioselective reactivity under standard conditions, streamlining access to complex carbocyclic frameworks in synthetic organic chemistry.
Ethyl 2-methyl-4-oxocyclohex-2-enecarboxylate serves as a versatile Michael acceptor and Diels–Alder dienophile, enabling efficient construction of substituted cyclohexane and heterocyclic scaffolds. Its conjugated enone system facilitates nucleophilic addition, while the ester group supports subsequent functionalization. Bench-stable and amenable to standard purification methods, it functions reliably in multistep syntheses for medicinal chemistry and natural product synthesis.
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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: