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Structure of 4971-56-6
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Furan-2,4(3H,5H)-dione features a reactive diketone core within a furan ring, enabling efficient participation in Diels-Alder cycloadditions and nucleophilic transformations. This bench-stable heterocycle integrates readily into complex molecular architectures, serving as a key scaffold for synthetic intermediates in natural product synthesis and materials science applications.
Furan-2,4(3H,5H)-dione serves as a versatile building block in synthetic organic chemistry, enabling efficient access to substituted furans and heterocyclic scaffolds. Its diketone functionality supports nucleophilic addition, condensation reactions, and transition-metal-catalyzed couplings. The compound exhibits good bench stability and facilitates straightforward purification, making it well-suited for iterative synthesis workflows in medicinal chemistry and process development.
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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 : H315-H319
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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: