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Structure of 1072141-30-0
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4-Bromo-3-chloro-5-nitropyridine features a tri-substituted pyridine core with complementary halogen and nitro groups enabling precise functionalization. The electron-deficient ring facilitates cross-coupling reactions, while the ortho-halogen arrangement supports sequential derivatization. This robust scaffold integrates efficiently into complex heterocyclic architectures under standard conditions.
4-Bromo-3-chloro-5-nitropyridine serves as a versatile building block in medicinal chemistry and heterocyclic synthesis, enabling selective cross-coupling reactions via its bromo and chloro substituents. The nitro group provides a handle for sequential reduction and functionalization, while the pyridine core offers predictable reactivity in palladium-catalyzed transformations. Its bench-stable nature and compatibility with diverse reaction conditions facilitate efficient construction of complex scaffolds in API development.
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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
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Precautionary Statements : P264-P270-P330-P405-P501
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Lot numbers can be found on the outside label of a product: