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Structure of 1115-30-6
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Diethyl acetylsuccinate serves as a key synthon in organic synthesis, featuring a β-keto ester moiety flanked by ethyl groups that enable controlled enolization and nucleophilic addition. This structure facilitates efficient C–C bond formation under mild conditions, making it valuable for constructing complex carbocyclic and heterocyclic frameworks in medicinal chemistry and natural product synthesis.
Diethyl acetylsuccinate serves as a versatile synthon in organic synthesis, enabling efficient construction of substituted succinates and heterocyclic scaffolds. Its dual ester functionality and α,β-unsaturated carbonyl system facilitate nucleophilic additions, Michael reactions, and cycloadditions under mild conditions. The compound exhibits excellent bench stability and is readily purified by distillation or column chromatography, making it well-suited for scalable laboratory workflows and downstream derivatization in medicinal chemistry campaigns.
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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: