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Structure of 88982-82-5
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4-Bromo-1,3-thiazole-2-carboxylic acid features a brominated thiazole ring with a carboxylic acid group at the 2-position, offering a versatile scaffold for bioactive molecule synthesis. The electron-withdrawing bromine enhances reactivity in cross-coupling and functionalization reactions. This bench-stable compound integrates readily into pharmaceutical intermediates and agrochemical development workflows.
4-Bromo-1,3-thiazole-2-carboxylic acid serves as a versatile building block in medicinal chemistry and heterocyclic synthesis. Its bromine substituent enables palladium-catalyzed cross-coupling reactions, while the carboxylic acid group facilitates amide formation, esterification, and derivatization. The molecule exhibits bench stability and good functional group tolerance, making it well-suited for modular synthesis of thiazole-based pharmacophores and API intermediates.
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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: