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Structure of 1256818-64-0
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5-Bromofuro[2,3-b]pyridin-3(2H)-one features a fused heterocyclic core combining furan and pyridinone motifs, offering a rigid, electron-deficient scaffold. This structure enables direct functionalization at the bromine site for cross-coupling reactions, while the lactam carbonyl provides polarity and hydrogen-bonding capability. The compound exhibits bench-stable handling under standard conditions and serves as a key intermediate in the synthesis of bioactive nitrogen-containing heterocycles.
5-Bromofuro[2,3-b]pyridin-3(2H)-one serves as a versatile heterocyclic building block for medicinal chemistry and materials science. Its bromine substituent enables palladium-catalyzed cross-coupling reactions, while the fused furo[2,3-b]pyridinone core provides structural rigidity and enhanced solubility. The compound exhibits excellent bench stability and facilitates efficient functionalization in standard synthetic workflows.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: