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Structure of 5470-17-7
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3-Bromo-2-chloro-5-nitropyridine features a tri-substituted pyridine core with complementary halogen and nitro functionalities, enabling selective cross-coupling and functionalization in late-stage diversification. The electron-deficient ring facilitates nucleophilic substitution under mild conditions, while the orthogonal reactivity of bromo and chloro groups allows sequential transformations. This scaffold delivers high stability and predictable regiochemistry in synthetic workflows.
3-Bromo-2-chloro-5-nitropyridine serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling selective cross-coupling reactions via its halogen substituents. The nitro group provides a handle for reduction to an amine, while the ortho-halogen arrangement facilitates controlled functionalization. Its bench-stable nature and compatibility with Pd-catalyzed coupling protocols make it well-suited for modular heterocycle construction and late-stage diversification in API development.
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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-H318
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Precautionary Statements : P264-P270-P280-P330-P405-P501
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Lot numbers can be found on the outside label of a product: