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Structure of 52090-89-8
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5-Chloro-3H-imidazo[4,5-b]pyridine is a bench-stable heterocyclic scaffold featuring a chlorinated imidazopyridine core. This electron-deficient system integrates readily into medicinal chemistry campaigns, serving as a key building block for kinase inhibitors and bioactive small molecules. The chlorine substituent enables site-specific functionalization via cross-coupling reactions.
5-Chloro-3H-imidazo[4,5-b]pyridine serves as a versatile heterocyclic building block in medicinal chemistry, enabling direct functionalization at the C5 position via palladium-catalyzed cross-coupling reactions. Its stable, electron-deficient core exhibits excellent compatibility with diverse reaction conditions and facilitates the construction of complex imidazopyridine scaffolds found in kinase inhibitors and other bioactive molecules. The chloro substituent provides a reliable handle for further derivatization, while the compound demonstrates robust bench stability and ease of purification.
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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: