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Structure of 933782-03-7
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This bromomethylthiazole derivative features a reactive methanol group flanked by an electron-deficient thiazole ring and a methyl substituent. It serves as a key intermediate in the synthesis of bioactive heterocycles, offering enhanced stability and selective functionalization under standard conditions.
(2-Bromo-4-methylthiazol-5-yl)methanol serves as a versatile building block for thiazole-based scaffolds, enabling efficient functionalization via nucleophilic substitution and cross-coupling reactions. The bromo group facilitates palladium-catalyzed transformations, while the pendant alcohol supports derivatization or protection strategies. Its bench-stable nature and compatibility with diverse reaction conditions make it a practical choice for 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: