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Structure of 1268521-33-0
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3-Bromo-2-chloro-5-nitropyridin-4-amine features a pyridine core functionalized with bromo, chloro, and nitro groups at key positions, enabling strategic coupling in cross-coupling reactions. The electron-deficient ring enhances reactivity in palladium-catalyzed transformations. This bench-stable derivative integrates readily into complex heterocyclic scaffolds for pharmaceutical and agrochemical development.
3-Bromo-2-chloro-5-nitropyridin-4-amine serves as a versatile building block for heterocyclic synthesis, enabling palladium-catalyzed cross-coupling reactions due to its bromine and amine functionalities. The nitro group provides a handle for selective reduction or further functionalization, while the chloro substituent offers orthogonal reactivity. Its bench-stable nature and compatibility with standard reaction conditions facilitate efficient assembly of complex pyridine-based scaffolds in medicinal chemistry and materials science applications.
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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: