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Structure of 67625-36-9
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Ethyl 5-chloroimidazo[1,2-a]pyridine-2-carboxylate features a chlorinated imidazopyridine core that enables direct functionalization at the 5-position. This electron-deficient heterocycle integrates readily into synthetic sequences requiring stable, bench-stable building blocks for medicinal chemistry and agrochemical development.
Ethyl 5-chloroimidazo[1,2-a]pyridine-2-carboxylate serves as a versatile building block for constructing imidazo[1,2-a]pyridine scaffolds prevalent in medicinal chemistry. The chloro substituent at the 5-position enables direct functionalization via palladium-catalyzed cross-coupling reactions. The ester group facilitates further derivatization or hydrolysis to the carboxylic acid. This compound exhibits good bench stability and is compatible with standard synthetic workflows, enabling efficient access to diverse heterocyclic architectures.
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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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362-P501
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Lot numbers can be found on the outside label of a product: