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Structure of 221352-74-5
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This fluorenylmethoxycarbonyl-protected pyrrolidine derivative features a sterically hindered, bench-stable scaffold ideal for peptide synthesis. The (2S,4S)-configuration ensures stereochemical fidelity, while the C-terminal carboxylic acid and Boc-protected amine enable sequential coupling in solid-phase workflows.
(2S,4S)-1-(((9H-Fluoren-9-yl)methoxy)carbonyl)-4-((tert-butoxycarbonyl)amino)pyrrolidine-2-carboxylic acid serves as a versatile chiral building block for peptide and heterocyclic synthesis. Its protected amine and carboxylic acid functionalities enable orthogonal deprotection and coupling strategies. The Fmoc group ensures stability under basic conditions, while the Boc-labile amine facilitates selective activation. This scaffold is well-suited for solid-phase peptide synthesis and the construction of bioactive pyrrolidine-containing compounds.
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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-H317
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Precautionary Statements : P261-P264-P270-P272-P280-P302+P352-P330-P362+P364-P501
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Lot numbers can be found on the outside label of a product: