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Structure of 252049-05-1
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This chiral fluorenylmethoxycarbonyl-protected amino acid derivative features a bench-stable, moisture-tolerant side chain ideal for solid-phase peptide synthesis. The (S)-configuration ensures stereochemical fidelity during coupling steps, while the fluoren-9-ylmethoxycarbonyl group enables efficient deprotection under mild basic conditions.
(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)(methyl)amino)pentanoic acid serves as a robust chiral building block for peptide synthesis, enabling efficient Nα-protection with orthogonal deprotection under mild conditions. Its fluorenylmethoxycarbonyl (Fmoc) group ensures high stability during storage and handling, while the methylamino functionality provides a well-defined side chain for downstream derivatization. The molecule exhibits excellent solubility in common organic solvents and facilitates clean coupling reactions, making it ideal for solid-phase and solution-phase peptide assembly 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 : 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: