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Structure of 41731-83-3
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Ethyl 2-bromothiazole-5-carboxylate features a brominated thiazole core that enables direct functionalization in cross-coupling reactions. The ester group enhances solubility and reactivity, while the electron-deficient heterocycle facilitates palladium-catalyzed transformations. This bench-stable reagent integrates efficiently into synthetic sequences requiring halogenated heterocyclic building blocks.
Ethyl 2-bromothiazole-5-carboxylate serves as a versatile building block in heterocyclic synthesis, enabling palladium-catalyzed cross-coupling reactions due to its well-defined bromine substituent. The thiazole core provides robust stability and compatibility with diverse functional groups, facilitating efficient derivatization for medicinal chemistry applications. Its bench-stable nature and straightforward purification support scalable synthesis workflows.
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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 : H317
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Precautionary Statements : P261-P272-P280-P302+P352-P363-P501
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Lot numbers can be found on the outside label of a product: