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Structure of 80353-98-6
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Ethyl 2-bromoimidazo[2,1-b]thiazole-6-carboxylate features a brominated imidazo-thiazole core with enhanced reactivity at the C2 position. This electron-deficient heterocycle integrates readily into transition-metal-catalyzed coupling reactions, enabling efficient construction of complex scaffolds in medicinal chemistry and materials synthesis.
Ethyl 2-bromoimidazo[2,1-b]thiazole-6-carboxylate serves as a versatile building block for the synthesis of imidazo[2,1-b]thiazole-based scaffolds. The bromine atom enables palladium-catalyzed cross-coupling reactions, while the ester functionality supports further transformations such as hydrolysis or reduction. This compound exhibits bench stability and facilitates efficient access to medicinally relevant heterocycles through well-established synthetic protocols.
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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 : H315-H319
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Precautionary Statements : P264-P280-P302+P352-P362+P364
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Lot numbers can be found on the outside label of a product: