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Structure of 220616-68-2
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2,6-Dibromopyridin-4-ol features a pyridinol core bearing bromine substituents at the 2 and 6 positions, creating a sterically congested, electron-deficient platform. The phenolic hydroxyl group enables hydrogen bonding and facilitates downstream functionalization. This scaffold offers enhanced stability under standard conditions and serves as a robust building block for advanced heterocyclic synthesis.
2,6-Dibromopyridin-4-ol serves as a versatile building block for the synthesis of functionalized pyridine derivatives and heterocyclic scaffolds. The compound exhibits enhanced reactivity at the C4 position due to the electron-withdrawing bromo groups, enabling efficient palladium-catalyzed cross-coupling reactions. Its bench-stable nature and tolerance to diverse functional groups facilitate straightforward incorporation into complex molecular architectures, particularly in medicinal chemistry and materials science applications.
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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: