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Structure of 1206708-88-4
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2,4-Dibromo-5-methylthiazole features a sterically accessible thiazole core with two bromine substituents at electron-deficient positions and a methyl group at C5, enabling direct functionalization in cross-coupling reactions. This bench-stable heterocycle integrates readily into bioactive scaffolds and materials architectures requiring halogenated building blocks.
2,4-Dibromo-5-methylthiazole serves as a versatile building block in heterocyclic synthesis, enabling efficient access to substituted thiazole scaffolds via palladium-catalyzed cross-coupling reactions. The bromine atoms at the 2- and 4-positions offer orthogonal reactivity for sequential functionalization, while the methyl group enhances stability and modulates electronic properties. Its bench-stable nature and compatibility with standard synthetic protocols make it ideal for medicinal chemistry campaigns and process-scale applications.
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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: