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Structure of 172690-48-1
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This fluorenylmethoxycarbonyl-protected amino acid derivative features a chiral (S)-configuration at the alpha carbon, enabling stereoselective peptide synthesis. The C-terminal acetamido group provides enhanced stability, while the fluoren-9-ylmethoxycarbonyl (Fmoc) moiety facilitates efficient orthogonal deprotection under mild basic conditions. This combination ensures high fidelity in solid-phase peptide assembly and simplifies purification workflows.
(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-5-acetamidopentanoic acid serves as a protected amino acid building block for peptide synthesis, enabling efficient incorporation of (S)-lysine analogs. The Fmoc group provides orthogonal protection with high stability and facile removal under mild basic conditions. The acetamido side chain offers enhanced solubility and functional group tolerance, while the carboxylic acid facilitates standard coupling reactions. This compound functions reliably in solid-phase and solution-phase workflows.
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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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: