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Structure of 58012-34-3
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Ethyl 4-oxocyclohexaneacetate features a cyclohexanone ring bearing an acetic ester side chain, delivering a versatile scaffold for synthetic transformations. The ketone and ester functionalities enable selective functionalization, while the cyclic framework provides rigidity beneficial in stereocontrolled synthesis. This compound serves as a key intermediate in the construction of complex natural products and pharmaceuticals.
Ethyl 4-oxocyclohexaneacetate serves as a versatile building block in synthetic organic chemistry, enabling efficient access to substituted cyclohexane derivatives. Its α,β-unsaturated ketone functionality facilitates Michael additions, aldol reactions, and transition-metal-catalyzed couplings. The ester group offers compatibility with standard manipulations including reduction, hydrolysis, and Grignard additions. Bench-stable and readily purified by distillation or chromatography, it functions effectively in multi-step syntheses of bioactive molecules and natural product analogs.
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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: