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Structure of 2350732-99-7
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This fluoren-9-ylmethoxycarbonyl-protected amino acid derivative serves as a key chiral building block for peptide synthesis. The (2S)-configuration ensures stereochemical fidelity, while the fluorenylmethoxycarbonyl group enables efficient, orthogonal protection of the amine. The phenyl-substituted aliphatic side chain provides enhanced hydrophobicity and structural rigidity, improving solubility in organic media and facilitating purification.
(2S)-2-(9H-Fluoren-9-ylmethoxycarbonylamino)-6-phenylhexanoic acid serves as a versatile chiral building block for peptide synthesis and medicinal chemistry applications. The fluorenylmethoxycarbonyl (Fmoc) group enables efficient, orthogonal protection of primary amines under mild conditions, while the phenyl-substituted aliphatic chain provides structural rigidity and enhanced metabolic stability. Its bench-stable nature and compatibility with standard coupling protocols facilitate straightforward purification and scalability in solid-phase and solution-phase syntheses.
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Lot numbers can be found on the outside label of a product: