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Structure of 1380245-88-4
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2-Bromo-3H-imidazo[4,5-b]pyridine features a fused heterocyclic core enabling direct integration into complex pharmaceutical scaffolds. The bromine substituent provides a reactive handle for palladium-catalyzed cross-coupling, facilitating rapid diversification in medicinal chemistry campaigns. This bench-stable, moisture-tolerant compound delivers high functional group compatibility and enables efficient access to bioactive nitrogen-rich architectures.
2-Bromo-3H-imidazo[4,5-b]pyridine serves as a versatile heterocyclic building block in medicinal chemistry, enabling efficient late-stage functionalization via palladium-catalyzed cross-coupling reactions. Its bromine substituent facilitates reliable coupling with boronic acids, stannanes, and other nucleophiles, while the imidazopyridine core provides structural rigidity and favorable pharmacophoric properties. The compound exhibits good bench stability and is readily purified by standard chromatographic methods, making it well-suited for iterative synthesis of complex scaffolds.
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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: