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Structure of 1168090-92-3
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Methyl 5-chloroimidazo[1,5-a]pyridine-6-carboxylate features a chlorinated imidazopyridine core with a methyl ester at the C6 position, enabling direct integration into heterocyclic synthesis. The electron-deficient aromatic system facilitates nucleophilic substitution and metal-catalyzed coupling reactions. This bench-stable compound serves as a key intermediate for bioactive molecule development, particularly in kinase inhibitor scaffolds.
Methyl 5-chloroimidazo[1,5-a]pyridine-6-carboxylate serves as a versatile building block for the synthesis of imidazo[1,5-a]pyridine derivatives, key scaffolds in medicinal chemistry. The chloro group at the 5-position enables palladium-catalyzed cross-coupling reactions, while the ester functionality supports selective transformations. Its bench-stable nature and compatibility with standard reaction conditions facilitate efficient access to functionalized heterocycles relevant to drug discovery and process 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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: