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Structure of 2260800-15-3
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This fluorenylmethoxycarbonyl-protected amino acid derivative features a chiral side chain with a methyl substituent, enabling selective incorporation into peptide sequences. The C-terminal carboxylic acid group supports efficient coupling reactions, while the Fmoc moiety ensures stable storage and orthogonal deprotection under mild basic conditions.
(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)(methyl)amino)-5-methylhexanoic acid serves as a robust chiral building block for peptide synthesis, enabling efficient incorporation of sterically hindered, branched side chains. The Fmoc-protected amine and pendant methyl group offer enhanced solubility and stability during coupling reactions, while the C5-methyl substituent provides defined stereochemical control. Its bench-stable nature and compatibility with standard SPPS protocols facilitate reliable synthesis of complex peptides and peptidomimetics.
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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: