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Structure of 50432-68-3
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4-Chloro-1-methyl-1H-imidazo[4,5-c]pyridine is a heterocyclic scaffold featuring a chlorine substituent and a methyl group at the 4- and 1-positions, respectively. This electron-deficient imidazopyridine core integrates readily into medicinal chemistry campaigns, serving as a key building block for kinase inhibitors and bioactive small molecules. The compound exhibits bench-stable handling characteristics and compatibility with standard cross-coupling protocols.
4-Chloro-1-methyl-1H-imidazo[4,5-c]pyridine serves as a versatile heterocyclic building block in medicinal chemistry, enabling efficient construction of fused imidazopyridine scaffolds. Its chlorine atom facilitates palladium-catalyzed cross-coupling reactions, while the methylated imidazole nitrogen enhances stability and modulates reactivity. The compound exhibits excellent bench stability and compatibility with common functional groups, making it well-suited for iterative synthesis workflows in API development.
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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: