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Structure of 959755-96-5
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Ethyl 4-bromo-1,3-thiazole-2-carboxylate features a brominated thiazole ring enabling direct functionalization in cross-coupling reactions. The ester group provides synthetic versatility, while the electron-deficient heterocycle enhances reactivity in palladium-catalyzed transformations. This bench-stable reagent integrates readily into complex molecule assembly.
Ethyl 4-bromo-1,3-thiazole-2-carboxylate serves as a versatile building block in heterocyclic synthesis, enabling palladium-catalyzed cross-coupling reactions due to its well-defined bromine handle. The molecule exhibits bench stability and facilitates efficient functionalization at the C4 position, making it valuable for constructing thiazole-based scaffolds in medicinal chemistry and agrochemical research. Its ethyl ester group supports further derivatization, enhancing utility in multi-step synthetic sequences.
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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: