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Structure of 371945-06-1
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Ethyl 3-aminofuro[2,3-b]pyridine-2-carboxylate features a fused heterocyclic core with a pendant amino group and ester functionality, enabling direct integration into medicinal chemistry campaigns. This bench-stable scaffold supports efficient derivatization and serves as a key intermediate for bioactive nitrogen-containing compounds.
Ethyl 3-aminofuro[2,3-b]pyridine-2-carboxylate serves as a versatile building block for furo[2,3-b]pyridine-based heterocycles, enabling efficient access to pharmaceutically relevant scaffolds. The amino and ester functionalities offer orthogonal reactivity, facilitating downstream derivatization via coupling, alkylation, or cyclization reactions. Bench-stable and readily purified by column chromatography, it functions effectively in multi-step synthesis workflows requiring functional group tolerance and predictable regiochemistry.
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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: