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Structure of 54045-76-0
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2-Bromothiazole-5-carboxylic acid features a brominated thiazole ring fused to a carboxylic acid group, enabling direct incorporation into heterocyclic scaffolds. The electron-deficient aromatic core facilitates electrophilic substitution and transition-metal-catalyzed coupling reactions. This bench-stable reagent delivers high functional group tolerance and serves as a key building block in medicinal chemistry and agrochemical synthesis.
2-Bromothiazole-5-carboxylic acid serves as a versatile building block for constructing thiazole-based heterocycles in medicinal chemistry and agrochemical research. Its bromine and carboxylic acid functionalities enable direct coupling reactions, including Pd-catalyzed cross-couplings and amide formation, with high functional group tolerance. The compound exhibits bench stability and facilitates straightforward purification, making it well-suited for 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 : 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: