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Structure of 170232-68-5
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2,4-Dibromothiazole-5-methanol features a brominated thiazole core with a reactive methanol handle, enabling direct functionalization in cross-coupling and derivatization workflows. The electron-deficient ring and orthogonal halogen sites support selective transformations under mild conditions.
2,4-Dibromothiazole-5-methanol serves as a versatile building block for heterocyclic synthesis, enabling efficient access to functionalized thiazole scaffolds. The bromo groups facilitate palladium-catalyzed cross-coupling reactions, while the methanol functionality offers a handle for derivatization or protection. Its bench-stable nature and compatibility with standard reaction conditions make it well-suited for iterative synthesis 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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: