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Structure of 23056-44-2
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4-Bromo-3-nitropyridine features a pyridine core bearing both bromo and nitro substituents at adjacent positions, enabling direct functionalization via cross-coupling or nucleophilic substitution. This electron-deficient heterocycle integrates readily into synthetic scaffolds for pharmaceuticals and agrochemicals, offering high reactivity under standard conditions.
4-Bromo-3-nitropyridine serves as a versatile building block in heterocyclic synthesis, enabling palladium-catalyzed cross-coupling reactions and nucleophilic substitution processes. The bromo group facilitates C–C bond formation under standard conditions, while the nitro group provides a directing effect for regioselective functionalization. Its bench-stable nature and compatibility with common protecting groups make it well-suited for multi-step synthesis of complex pyridine derivatives and pharmaceutical intermediates.
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GHS Pictogram :
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GHS No : GHS05
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Signal Word : Danger
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UN#: 1759
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P280-P302+P352
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Lot numbers can be found on the outside label of a product: