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Structure of 189249-10-3
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This fluorenylmethoxycarbonyl-protected pyrrolidine derivative features a chiral (2S,4S) core with a hydroxyl group at C4 and a carboxylic acid at C2, enabling direct incorporation into peptide synthesis workflows. The Fmoc moiety provides orthogonal protection, while the stereochemistry ensures high diastereoselectivity in coupling reactions. Designed for efficient solid-phase and solution-phase assembly of complex peptidomimetics and cyclic peptides.
(2S,4S)-1-(((9H-Fluoren-9-yl)methoxy)carbonyl)-4-hydroxypyrrolidine-2-carboxylic acid serves as a chiral building block for peptide synthesis and medicinal chemistry applications. The Fmoc group enables orthogonal protection in solid-phase peptide synthesis, while the C4 hydroxyl group provides a site for derivatization or stereocontrolled transformations. Its bench-stable nature and compatibility with standard coupling conditions facilitate efficient incorporation into complex molecular architectures.
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: