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Structure of 1194374-25-8
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2-Bromo-5-methylthiazole-4-carboxylic acid features a brominated thiazole core with a methyl group at the 5-position and a carboxylic acid at the 4-position, enabling direct coupling in synthetic routes. This electron-deficient heterocycle integrates readily into bioactive scaffolds, offering enhanced reactivity for C–C and C–heteroatom bond formation under standard conditions.
2-Bromo-5-methylthiazole-4-carboxylic acid serves as a versatile building block in heterocyclic synthesis, enabling efficient access to thiazole-based scaffolds prevalent in medicinal chemistry. Its bromine and carboxylic acid functionalities support diverse transformations, including palladium-catalyzed cross-couplings and derivatization via amide or ester formation. The molecule exhibits good bench stability and facilitates straightforward purification, making it well-suited for iterative synthesis campaigns and API intermediate development.
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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: