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Structure of 214852-45-6
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This fluorenylmethoxycarbonyl-protected pyrrolidine derivative features a stereodefined hydroxyl group at the C4 position, enabling direct incorporation into peptide synthesis. The bench-stable, moisture-tolerant scaffold facilitates efficient N-terminal functionalization in solid-phase and solution-phase workflows.
(2R,4R)-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, while the 4-hydroxy functionality provides a site for derivatization or incorporation into bioactive scaffolds. Bench-stable and readily purified by chromatography, it facilitates efficient coupling reactions in solid-phase and solution-phase workflows.
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GHS Pictogram :
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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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: