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Structure of 90993-26-3
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7-Bromo-1H-imidazo[4,5-c]pyridine is a heterocyclic scaffold featuring a brominated imidazopyridine core with enhanced electron-deficient character. This platform integrates readily into transition-metal-catalyzed coupling reactions and serves as a key building block in medicinal chemistry for targeted kinase inhibition and bioactive molecule design.
7-Bromo-1H-imidazo[4,5-c]pyridine serves as a versatile heterocyclic building block in medicinal chemistry, enabling efficient construction of bioactive scaffolds via palladium-catalyzed cross-coupling reactions. The bromo group facilitates reliable functionalization under standard Suzuki and Buchwald-Hartwig conditions, while the fused imidazopyridine core provides structural rigidity and favorable pharmacophoric properties for target-directed synthesis. Bench-stable and readily purified by recrystallization, it functions effectively in multi-step synthetic sequences requiring high functional group tolerance and predictable reactivity.
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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: