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Structure of 911052-85-2
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This bench-stable (5-bromothiazol-2-yl)methanol features a reactive aldehyde handle flanked by a brominated thiazole ring, enabling direct coupling in cross-coupling and bioconjugation workflows. The electron-deficient heterocycle enhances reactivity in palladium-catalyzed transformations.
(5-Bromothiazol-2-yl)methanol serves as a versatile building block for thiazole-based heterocycles, enabling direct functionalization at the 2-position via nucleophilic substitution or coupling reactions. The bromine atom facilitates Pd-catalyzed cross-coupling, while the pendant hydroxymethyl group allows for oxidation to aldehyde or carboxylic acid, or conversion to esters and amides. Its bench-stable nature and compatibility with diverse reaction conditions make it a practical reagent for medicinal chemistry and materials synthesis 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 : P233-P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362-P405-P501
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Lot numbers can be found on the outside label of a product: