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Structure of 614-99-3
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Ethyl 2-furancarboxylate serves as a versatile heterocyclic building block in synthetic organic chemistry. This bench-stable ester integrates readily into cross-coupling and condensation reactions, offering high reactivity at the furan ring’s C2 position. The ethyl ester group enables straightforward functionalization, while the electron-rich furan moiety supports diverse transformations under mild conditions.
Ethyl 2-furancarboxylate serves as a versatile building block in heterocyclic synthesis, enabling efficient access to furan-based scaffolds via coupling and functionalization reactions. Its ester group facilitates nucleophilic addition and metal-catalyzed transformations, while the furan ring provides inherent stability and compatibility with diverse reaction conditions. Widely employed in medicinal chemistry and materials science, it functions as a reliable precursor for bioactive molecules and conjugated systems.
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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: