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*For research and further manufacturing use only, not for direct human use.
Structure of 1018332-23-4
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This protected pyrrolidine derivative features orthogonal shielding via tert-butoxycarbonyl and fluorenylmethoxycarbonyl groups, enabling sequential deprotection in peptide synthesis. The rigid pyrrolidine core enhances conformational control in macrocyclic systems, while the bench-stable, moisture-tolerant structure simplifies handling under standard conditions.
(2R,4S)-1-[(tert-Butoxy)carbonyl]-4-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)pyrrolidine-2-carboxylic acid serves as a key chiral building block for peptide synthesis and medicinal chemistry campaigns. Its dual Boc and Fmoc protecting groups enable orthogonal deprotection strategies, while the pyrrolidine core facilitates incorporation into bioactive scaffolds. The compound exhibits excellent bench stability, simplifies purification via standard chromatography, and participates reliably in coupling reactions under mild conditions.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: