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Structure of 131052-44-3
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5-(Chloromethyl)thiazole hydrochloride features a reactive chloromethyl group attached to the thiazole ring, enabling efficient functionalization in synthetic workflows. This bench-stable, moisture-tolerant reagent integrates readily into heterocyclic architectures and serves as a key intermediate for pharmaceutical and agrochemical derivatization.
5-(Chloromethyl)thiazole hydrochloride serves as a versatile building block for constructing thiazole-based scaffolds in medicinal chemistry and materials science. The chloromethyl group enables efficient nucleophilic substitution, facilitating C–C and C–heteroatom bond formation under mild conditions. Its stability under standard bench handling and compatibility with diverse functional groups make it ideal for iterative synthesis workflows. Functions as a key intermediate in the preparation of bioactive heterocycles and functionalized polymers.
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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#: 1759
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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-P363-P405-P501
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Lot numbers can be found on the outside label of a product: