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Structure of 21080-80-8
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Ethyl 4-cyclopropyl-2,4-dioxobutanoate features a reactive 1,3-dicarbonyl scaffold flanked by a cyclopropyl substituent, enabling efficient enolization and nucleophilic addition. This bench-stable reagent integrates readily into multicomponent condensations and heterocycle syntheses, delivering high functional group tolerance under standard conditions.
Ethyl 4-cyclopropyl-2,4-dioxobutanoate serves as a versatile synthon in heterocyclic synthesis, enabling efficient access to substituted pyrrolidines and other nitrogen-containing scaffolds via Michael addition or cyclocondensation reactions. Its α,β-unsaturated β-ketoester functionality exhibits excellent functional group tolerance and bench stability, facilitating straightforward purification and integration into multi-step sequences. The cyclopropyl substituent imparts distinct stereochemical control in cyclization processes, enhancing its utility in medicinal chemistry lead optimization.
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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: