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Structure of 2304413-31-6
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(S)-2-(N-Fmoc-N-methyl-amino)-3-cyclopropylpropanoic acid is a chiral building block featuring a cyclopropyl group that imparts conformational rigidity and enhanced metabolic stability. The Fmoc-protected amine enables efficient solid-phase peptide synthesis, while the N-methyl substitution reduces hydrogen-bonding capacity and improves membrane permeability. This scaffold integrates readily into bioactive peptides requiring tailored lipophilicity and structural constraint.
(S)-2-(N-Fmoc-N-methyl-amino)-3-cyclopropylpropanoic acid serves as a valuable chiral building block for peptide synthesis, enabling the incorporation of a sterically constrained cyclopropyl group at the β-position. The Fmoc group provides orthogonal protection for amine functionality, while the N-methyl substitution enhances metabolic stability and modulates conformational flexibility. This derivative exhibits excellent bench stability, facilitates efficient purification by standard chromatographic methods, and participates reliably in standard coupling protocols.
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Lot numbers can be found on the outside label of a product: