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Structure of 1187236-18-5
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Ethyl 7-bromoimidazo[1,2-a]pyridine-2-carboxylate features a brominated imidazopyridine core with enhanced reactivity at the C7 position. This electron-deficient heterocycle integrates readily into transition-metal-catalyzed coupling reactions. The ester functionality enables further derivatization, supporting rapid access to bioactive scaffolds in medicinal chemistry and materials science.
Ethyl 7-bromoimidazo[1,2-a]pyridine-2-carboxylate serves as a versatile building block for the synthesis of imidazopyridine-based scaffolds commonly found in medicinal chemistry. The bromine at the C7 position enables palladium-catalyzed cross-coupling reactions, while the ester functionality supports further derivatization via hydrolysis or reduction. Its bench-stable nature and compatibility with standard reaction conditions facilitate efficient incorporation into complex molecular 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-P405
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Lot numbers can be found on the outside label of a product: