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Structure of 4487-59-6
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2-Bromo-5-nitropyridine features a bromine atom at the 2-position and a nitro group at the 5-position on the pyridine ring, creating a highly functionalized heterocycle. This electronic asymmetry enables selective cross-coupling reactions and facilitates incorporation into complex molecular architectures. The molecule exhibits enhanced reactivity in palladium-catalyzed transformations due to the electron-withdrawing nature of both substituents. Its bench-stable solid form ensures reliable handling under standard laboratory conditions.
2-Bromo-5-nitropyridine serves as a versatile building block in heterocyclic synthesis, enabling palladium-catalyzed cross-coupling reactions due to its compatible bromine and nitro functionalities. The nitro group facilitates subsequent reduction and functionalization, while the pyridine core provides orthogonal reactivity for medicinal chemistry applications. Bench-stable and readily purified by recrystallization, it functions efficiently in standard coupling protocols and scaffold elaboration workflows.
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GHS Pictogram :
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GHS No : GHS06
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Signal Word : Danger
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UN#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H301-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: