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Structure of 139262-20-7
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This fluoren-9-ylmethoxycarbonyl-protected pyrrolidine derivative features a stereodefined hydroxyl group at C4 and a carboxylic acid at C2, enabling direct incorporation into peptide chains via solid-phase synthesis. The Fmoc group ensures stable handling and efficient deprotection under mild basic conditions.
(2R,4S)-1-(((9H-Fluoren-9-yl)methoxy)carbonyl)-4-hydroxypyrrolidine-2-carboxylic acid serves as a stereochemically defined building block for the synthesis of peptidomimetics and bioactive heterocycles. The fluorenylmethoxycarbonyl (Fmoc) group enables efficient orthogonal protection during solid-phase peptide synthesis, while the C4 hydroxyl supports selective derivatization and cyclization reactions. Its bench-stable nature and compatibility with standard coupling conditions facilitate reliable incorporation into complex molecular architectures.
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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: