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Structure of 942947-95-7
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5-Bromo-4-chloro-3-nitropyridin-2-amine features a densely functionalized pyridine core with bromo, chloro, and nitro groups positioned for orthogonal reactivity. This electron-deficient heterocycle enables selective cross-coupling and nucleophilic substitution under standard conditions, serving as a key intermediate in the synthesis of advanced pharmaceuticals and agrochemicals.
5-Bromo-4-chloro-3-nitropyridin-2-amine serves as a versatile building block in heterocyclic synthesis, enabling sequential functionalization via cross-coupling and nucleophilic substitution. The nitro group facilitates reduction to an amine for further derivatization, while the bromo and chloro substituents support palladium-catalyzed coupling reactions. Its bench-stable nature and orthogonal reactivity profile make it well-suited for modular assembly of complex pyridine-based scaffolds in medicinal chemistry and agrochemical research.
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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: