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Structure of 41302-34-5
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Methyl 2-oxocyclohexane-1-carboxylate features a cyclohexanone ring with a strategically positioned ester group, enabling direct functionalization at the alpha carbon. This configuration supports efficient enolization and subsequent nucleophilic substitution, making it ideal for constructing complex carbocyclic frameworks in natural product synthesis and medicinal chemistry applications.
Methyl 2-oxocyclohexane-1-carboxylate serves as a versatile building block in synthetic organic chemistry, enabling efficient access to cyclohexanone derivatives and functionalized heterocycles. Its α,β-unsaturated carbonyl system facilitates Michael additions, aldol condensations, and metal-catalyzed couplings. The ester group provides a handle for selective reduction or hydrolysis, while the cyclic ketone offers stability and predictable reactivity under standard conditions. This compound is valued for its bench-stable nature and compatibility with diverse transformation protocols in medicinal chemistry and process development workflows.
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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: