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Structure of 54396-74-6
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Methyl 3-oxocyclohex-1-enecarboxylate features a conjugated enone system flanked by a carbonyl and ester group, enabling efficient Michael additions and Diels-Alder cycloadditions. This bench-stable, moisture-tolerant reagent integrates readily into complex molecule synthesis workflows.
Methyl 3-oxocyclohex-1-enecarboxylate serves as a versatile building block in synthetic organic chemistry, enabling efficient access to functionalized cyclohexane derivatives. Its conjugated enone system facilitates Michael additions, Diels-Alder reactions, and selective reductions, while the ester group supports further transformations such as hydrolysis or nucleophilic acyl substitution. Bench-stable and readily purified by distillation or chromatography, it functions effectively in multi-step syntheses of natural products and pharmaceutical intermediates.
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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+P364-P405-P501
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Lot numbers can be found on the outside label of a product: