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Structure of 67443-38-3
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5-Bromo-2-chloro-3-nitropyridine features a tri-functional pyridine core with distinct halogen and nitro substituents enabling precise diversification in heterocyclic synthesis. The electron-deficient ring facilitates nucleophilic substitution, while the bromo and chloro groups offer orthogonal reactivity for sequential coupling. This scaffold integrates readily into pharmaceutical intermediates and functional materials under standard conditions.
5-Bromo-2-chloro-3-nitropyridine serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its complementary halogen reactivity. The nitro group provides a handle for selective reduction and downstream functionalization, while the ortho-chloro and bromo substituents offer orthogonal reactivity for sequential transformations. Its bench-stable crystalline form facilitates handling and purification, making it well-suited for multi-step synthesis of heterocyclic scaffolds and API intermediates.
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GHS Pictogram :
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GHS No : GHS05,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-H318-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362-P405-P501
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Lot numbers can be found on the outside label of a product: