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Structure of 145015-15-2
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(2-Chlorothiazol-5-yl)methanol features a chlorinated thiazole core bearing a reactive hydroxymethyl group, enabling direct functionalization in synthetic routes. This bench-stable scaffold integrates readily into bioactive molecule frameworks, particularly where halogenated heterocycles enhance target affinity or metabolic stability.
(2-Chlorothiazol-5-yl)methanol serves as a versatile building block for thiazole-based heterocycles, enabling efficient functionalization at the 5-position. Its benzylic-like alcohol functionality facilitates oxidation to the aldehyde or ester, and it participates reliably in coupling reactions with amines, nucleophiles, and transition metal catalysts. The chloro substituent provides orthogonal reactivity for palladium-catalyzed cross-coupling, supporting modular synthesis of bioactive scaffolds. Bench-stable and amenable to standard purification methods, it functions effectively 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: