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Structure of 6317-49-3
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Diethyl 4-oxoheptanedioate serves as a key synthon in the construction of complex carbocycles and heterocycles, featuring a β-keto ester moiety flanked by two ester groups. This structural motif enables efficient enolization and subsequent cyclization under mild conditions, facilitating rapid access to fused ring systems in natural product synthesis and medicinal chemistry applications.
Diethyl 4-oxoheptanedioate serves as a versatile bis-β-keto ester building block in synthetic organic chemistry, enabling efficient construction of complex heterocyclic scaffolds and polyfunctional intermediates. Its dual electrophilic carbonyl centers facilitate sequential condensation reactions, including Claisen and Michael-type additions, with excellent functional group tolerance and bench stability. The molecule’s well-defined reactivity profile makes it particularly valuable for the synthesis of biologically relevant frameworks such as γ-lactones, pyrones, and substituted cyclohexanones under standard laboratory conditions.
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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 : H227-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: