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Structure of 56355-61-4
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Methyl 2-bromo-5-methylthiazole-4-carboxylate features a brominated thiazole core with dual functional handles: a methyl ester for derivatization and a bromine atom enabling cross-coupling reactions. This bench-stable, moisture-tolerant reagent integrates efficiently into synthetic sequences requiring regioselective transformations.
Methyl 2-bromo-5-methylthiazole-4-carboxylate serves as a versatile building block in heterocyclic synthesis, enabling palladium-catalyzed cross-coupling reactions due to its reactive bromo group. The methylthiazole core provides enhanced stability and orthogonality in multi-step sequences, while the ester functionality allows for selective derivatization. Its bench-stable nature and compatibility with standard reaction conditions make it ideal for constructing thiazole-based scaffolds in medicinal chemistry and process development workflows.
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GHS Pictogram :
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GHS No : GHS06
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Signal Word : Danger
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UN#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H301
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Precautionary Statements : P264-P270-P330-P405-P501
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Lot numbers can be found on the outside label of a product: