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Structure of 321371-29-3
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Methyl 2-(chloromethyl)thiazole-4-carboxylate features a reactive chloromethyl group flanked by a thiazole ring and ester functionality, enabling direct functionalization in synthetic sequences. This bench-stable reagent integrates readily into heterocyclic scaffolds under mild conditions, serving as a key intermediate for medicinal chemistry and materials science applications.
Methyl 2-(chloromethyl)thiazole-4-carboxylate serves as a versatile building block in synthetic organic chemistry, enabling efficient construction of thiazole-based scaffolds. The chloromethyl group facilitates nucleophilic substitution reactions, while the ester functionality supports further transformations such as hydrolysis or reduction. Its bench-stable nature and compatibility with diverse reaction conditions make it well-suited for medicinal chemistry campaigns and process development workflows.
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GHS Pictogram :
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GHS No : GHS05,GHS07
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Signal Word : Danger
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UN#: 3261
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Class : 8
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Packing Group : Ⅱ
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Hazard Statements : H302-H314
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Precautionary Statements : P260-P264-P270-P280-P301+P330+P331-P304+P340-P330-P363-P405-P501
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Lot numbers can be found on the outside label of a product: