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Structure of 2144-37-8
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Methyl 5-(chloromethyl)furan-2-carboxylate features a reactive chloromethyl group flanked by a furan ring and ester functionality, enabling direct functionalization in late-stage diversification. This bench-stable reagent integrates readily into synthetic sequences requiring site-specific alkylation or cross-coupling transformations under mild conditions.
Methyl 5-(chloromethyl)furan-2-carboxylate serves as a versatile building block in synthetic organic chemistry, enabling efficient functionalization at the furan C5 position. The chloromethyl group facilitates nucleophilic substitution reactions, while the ester functionality supports downstream transformations such as hydrolysis or reduction. Its bench-stable nature and compatibility with diverse reaction conditions make it valuable for constructing heterocyclic scaffolds and complex molecular architectures in medicinal chemistry and process development workflows.
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GHS Pictogram :
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GHS No : GHS05
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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 : H314
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Precautionary Statements : P260-P264-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: