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Structure of 53662-83-2
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Diethyl furan-2,5-dicarboxylate serves as a versatile diester scaffold for constructing heterocyclic architectures. The furan core imparts electron-rich character, enabling efficient participation in cycloaddition and transition-metal-catalyzed coupling reactions. This bench-stable reagent integrates readily into synthetic sequences requiring planar, conjugated intermediates with predictable reactivity profiles under standard conditions.
Diethyl furan-2,5-dicarboxylate serves as a versatile synthon in heterocyclic synthesis, enabling efficient access to functionalized furan derivatives via standard ester manipulations. Its conjugated diester framework facilitates Diels-Alder reactions and transition-metal-catalyzed couplings, while exhibiting good bench stability and ease of purification. Functions effectively in the construction of bioactive scaffolds and advanced intermediates for pharmaceutical development.
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Lot numbers can be found on the outside label of a product: