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Structure of 1417789-17-3
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(S)-Fmoc-2-amino-5-(tritylthio)-pentanoic acid is a chiral building block featuring a protected amine and a sulfur-stabilized side chain. This derivative enables selective conjugation in peptide synthesis, where the tritylthio group offers robust protection under standard conditions. The Fmoc moiety facilitates orthogonal deprotection, streamlining sequence assembly. Its bench-stable nature supports reliable handling in synthetic workflows.
(S)-Fmoc-2-amino-5-(tritylthio)-pentanoic acid serves as a valuable building block for the synthesis of peptidomimetics and cysteine-containing peptide segments. The Fmoc group enables efficient solid-phase peptide synthesis, while the tritylthio protecting group offers orthogonal stability and facile removal under mild acidic conditions. This compound facilitates site-specific incorporation of functionalized cysteine surrogates with excellent bench stability and compatibility across standard coupling protocols.
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Lot numbers can be found on the outside label of a product: