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Structure of 1013883-02-7
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This fluorenonylmethoxycarbonyl-protected amino acid derivative features a chiral benzylic center and a para-substituted phenyl ether side chain, enabling direct incorporation into peptide sequences. The C-terminal carboxylic acid group supports efficient coupling under standard conditions, while the robust fluorenylmethoxy carbonyl (Fmoc) moiety ensures stable protection during synthesis.
(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-(2-((tert-butoxycarbonyl)amino)ethoxy)phenyl)propanoic acid serves as a versatile chiral building block for peptide synthesis and medicinal chemistry campaigns. Its fluorenylmethoxycarbonyl (Fmoc) and tert-butyl carbamate (Boc) protecting groups enable orthogonal deprotection strategies. The pendant phenethyl ether moiety provides structural diversity for drug-like scaffolds, while the alpha-amino acid core facilitates efficient coupling reactions with excellent functional group tolerance and bench stability.
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Lot numbers can be found on the outside label of a product: