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Structure of 24485-01-6
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5,7-Dichloro-3H-imidazo[4,5-b]pyridine is a heterocyclic scaffold featuring two chlorine substituents at electron-rich positions, enhancing its utility in medicinal chemistry. This bench-stable, moisture-tolerant core integrates readily into kinase inhibitors and bioactive scaffolds, offering improved binding affinity through strategic halogen bonding interactions.
5,7-Dichloro-3H-imidazo[4,5-b]pyridine serves as a versatile heterocyclic building block in medicinal chemistry, enabling the synthesis of kinase inhibitors and other bioactive scaffolds. Its dichloro substitution pattern facilitates efficient late-stage functionalization via palladium-catalyzed cross-coupling reactions. The compound exhibits good bench stability, moderate solubility in common organic solvents, and compatibility with standard protecting group strategies, making it well-suited for iterative synthesis workflows in drug discovery programs.
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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: