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Structure of 15971-92-3
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Ethyl 3-cyclohexyl-3-oxopropanoate features a sterically hindered β-keto ester core that enables reliable enolization and nucleophilic addition reactions. This bench-stable compound integrates seamlessly into synthetic sequences requiring controlled carbonyl reactivity, particularly in the construction of cyclic ketones and functionalized heterocycles under mild conditions.
Ethyl 3-cyclohexyl-3-oxopropanoate serves as a versatile building block in synthetic organic chemistry, enabling efficient construction of substituted cyclohexane derivatives via aldol-type condensations and Michael additions. Its α,β-unsaturated ester functionality facilitates conjugate addition reactions, while the cyclohexyl group provides steric and electronic modulation. The compound exhibits excellent bench stability and is readily purified by distillation or chromatography, making it well-suited for iterative synthesis workflows in medicinal chemistry and natural product synthesis.
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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: