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Structure of 176486-63-8
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This fluorenylmethoxycarbonyl-protected pyrrolidine derivative features a sterically hindered, bench-stable scaffold ideal for peptide synthesis. The (2S,4R)-configured core integrates seamlessly into complex sequences, while the tert-butoxycarbonyl and fluorenylmethoxycarbonyl groups enable orthogonal protection and efficient deprotection under standard conditions.
(2S,4R)-4-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-1-(tert-butoxycarbonyl)pyrrolidine-2-carboxylic acid serves as a key chiral building block for the synthesis of pyrrolidine-containing peptides and heterocyclic scaffolds. The Fmoc and Boc groups provide orthogonal protection for amine and carboxylic acid functionalities, enabling sequential coupling in solid-phase peptide synthesis. Bench-stable and readily purified by standard chromatographic methods, it facilitates efficient access to bioactive compounds through established coupling protocols.
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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-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: