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Structure of 438190-89-7
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6-Bromo-2-chloro-3H-imidazo[4,5-b]pyridine is a heterocyclic scaffold featuring bromo and chloro substituents at strategic positions, enabling direct functionalization in cross-coupling reactions. This electron-deficient imidazopyridine serves as a key intermediate for constructing bioactive molecules in medicinal chemistry and agrochemical development.
6-Bromo-2-chloro-3H-imidazo[4,5-b]pyridine serves as a versatile heterocyclic building block for medicinal chemistry and catalytic cross-coupling applications. The molecule’s dual halogenation pattern enables sequential functionalization via Pd-catalyzed coupling reactions, with the bromo group typically exhibiting higher reactivity than the chloro substituent. Its stability under standard reaction conditions and compatibility with diverse functional groups make it well-suited for constructing complex pharmaceutical scaffolds and kinase inhibitor cores in high-throughput synthesis 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: