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Structure of 408352-48-7
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4,6-Dibromopyridin-2-amine features two bromine substituents at the 4 and 6 positions of the pyridine ring, flanking a strategically placed amine group. This arrangement enables direct coupling in cross-coupling reactions, delivering functionalized heterocycles with high regiocontrol. The molecule exhibits robust stability under standard conditions and integrates readily into synthetic sequences requiring halogenated building blocks.
4,6-Dibromopyridin-2-amine serves as a versatile building block in medicinal chemistry and materials science, enabling efficient access to substituted pyridine scaffolds via palladium-catalyzed cross-coupling reactions. The strategically positioned bromine atoms facilitate sequential functionalization, while the amino group provides a handle for derivatization or metal coordination. Its bench-stable nature and compatibility with standard coupling protocols make it a practical choice for constructing complex heterocyclic architectures in API development and advanced synthetic workflows.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: