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Structure of 99073-88-8
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Ethyl 2-bromobenzo[d]thiazole-6-carboxylate features a brominated benzo[d]thiazole core with a carboxylate ester handle, enabling direct functionalization in transition-metal-catalyzed cross-coupling reactions. The electron-deficient heterocycle pairs effectively with palladium systems, delivering high yields in C–C bond formation. This bench-stable reagent streamlines access to complex thiazole-based scaffolds for medicinal chemistry and materials synthesis.
Ethyl 2-bromobenzo[d]thiazole-6-carboxylate serves as a versatile building block for constructing bioactive heterocycles, enabling palladium-catalyzed cross-coupling reactions with broad functional group tolerance. Its bromo substituent facilitates C–C bond formation under standard Suzuki, Stille, or Negishi conditions, while the ester group supports further derivatization. The molecule exhibits excellent bench stability and ease of purification, making it well-suited for iterative synthesis in medicinal chemistry and process development 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 : 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: