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Structure of 2528-00-9
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Ethyl 5-(chloromethyl)furan-2-carboxylate features a reactive chloromethyl group at the 5-position of a furan ring, enabling direct functionalization in synthetic sequences. This bench-stable, moisture-tolerant reagent integrates readily into C–C and C–heteroatom bond-forming reactions, offering efficient access to substituted furan architectures under standard conditions.
Ethyl 5-(chloromethyl)furan-2-carboxylate serves as a versatile building block for furan-based heterocycles, enabling efficient functionalization at the C5 position. The chloromethyl group facilitates nucleophilic substitution, allowing rapid access to diverse derivatives via displacement reactions. Its bench-stable nature and compatibility with standard synthetic protocols make it well-suited for medicinal chemistry campaigns and process-scale applications.
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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#: 3265
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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: