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Structure of 14676-03-0
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This protected amino acid derivative features a furan-2-yl group flanked by a tert-butoxycarbonyl (Boc) amine and a carboxylic acid, enabling direct incorporation into peptide chains. The Boc moiety ensures stability during synthesis, while the electron-rich furan ring enhances reactivity in coupling reactions under standard conditions.
3-((tert-Butoxycarbonyl)amino)-3-(furan-2-yl)propanoic acid serves as a versatile building block for the synthesis of furan-containing amino acid derivatives. The tert-butoxycarbonyl (Boc) group provides excellent stability and orthogonal deprotection compatibility, while the pendant furan moiety enables facile incorporation into heterocyclic scaffolds. Its well-defined reactivity facilitates straightforward peptide coupling and functionalization under standard conditions, offering reliable access to biologically relevant motifs in medicinal chemistry and process development.
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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: