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Structure of 1093106-54-7
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1-(2-Bromo-4-methylthiazol-5-yl)ethan-1-one features a brominated thiazole core paired with a ketone-functionalized ethyl side chain, enabling direct coupling in cross-coupling reactions. The electron-deficient thiazole ring enhances reactivity in palladium-catalyzed transformations, while the methyl group provides steric modulation. This scaffold integrates efficiently into complex heterocyclic architectures under standard conditions.
1-(2-Bromo-4-methylthiazol-5-yl)ethan-1-one serves as a versatile building block in heterocyclic synthesis, enabling direct functionalization at the thiazole C5 position. The bromo substituent facilitates palladium-catalyzed cross-coupling reactions, while the acetyl group provides a handle for further derivatization via condensation or reduction. Its bench-stable crystalline form and compatibility with standard reaction conditions make it well-suited for iterative synthesis of thiazole-based scaffolds in medicinal chemistry and process development 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: