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Structure of 1042141-37-6
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Methyl 2-bromoimidazo[1,2-a]pyridine-6-carboxylate is a heterocyclic building block featuring a brominated imidazopyridine core paired with a methyl ester handle. This scaffold enables direct functionalization in cross-coupling reactions and integrates readily into bioactive molecule frameworks. The bromine atom serves as a reactive site for palladium-catalyzed transformations, while the ester group offers versatility in subsequent derivatization. The compound exhibits stability under standard conditions and is compatible with diverse synthetic workflows.
Methyl 2-bromoimidazo[1,2-a]pyridine-6-carboxylate serves as a versatile building block for the synthesis of imidazo[1,2-a]pyridine-based scaffolds. The bromo group enables palladium-catalyzed cross-coupling reactions, while the ester functionality supports further derivatization via hydrolysis or reduction. Its bench-stable nature and compatibility with diverse reaction conditions facilitate efficient access to functionalized heterocycles relevant in medicinal chemistry and materials science.
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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: