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Structure of 167275-47-0
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(S)-1-(((9H-Fluoren-9-yl)methoxy)carbonyl)-2-methylpyrrolidine-2-carboxylic acid delivers a sterically hindered, bench-stable chiral building block for peptide synthesis. The fluorenylmethoxycarbonyl (Fmoc) group enables orthogonal protection, while the methylated pyrrolidine core provides conformational rigidity and enhanced solubility. This derivative supports efficient coupling reactions under standard conditions.
(S)-1-(((9H-Fluoren-9-yl)methoxy)carbonyl)-2-methylpyrrolidine-2-carboxylic acid serves as a robust chiral building block for peptide synthesis, enabling efficient N-terminal protection and stereocontrol. The Fmoc group provides excellent bench stability and facilitates mild deprotection under basic conditions. Its 2-methylpyrrolidine scaffold offers enhanced conformational rigidity and favorable solubility, supporting high-yielding couplings in standard solid-phase protocols. This compound functions reliably in the construction of complex peptide architectures and cyclic peptide motifs.
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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: