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Structure of 140430-54-2
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(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-((2,4-dinitrophenyl)amino)propanoic acid serves as a robust chiral building block for peptide synthesis, combining the stability of Fmoc protection with the electron-withdrawing character of the 2,4-dinitrophenyl group. Its orthogonality enables selective deprotection and facilitates efficient coupling in solid-phase workflows. The dinitrophenyl moiety enhances solubility and aids purification via chromatography, while the (S)-configuration ensures stereochemical fidelity in target molecule construction.
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Lot numbers can be found on the outside label of a product: