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Structure of 501331-02-8
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(R)-2-(((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)methyl)-3-methylbutanoic acid is a chiral, bench-stable amino acid derivative featuring a fluorenylmethoxycarbonyl (Fmoc) protecting group. This moiety enables efficient incorporation into peptide chains under standard coupling conditions while maintaining stereochemical integrity during synthesis. The branched aliphatic side chain enhances solubility and reduces aggregation in solid-phase peptide assembly workflows.
(R)-2-(((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)methyl)-3-methylbutanoic acid serves as a robust chiral building block for peptide synthesis, offering high stereopurity and bench stability. The Fmoc group enables efficient orthogonal protection during solid-phase peptide coupling, while the branched aliphatic side chain provides structural rigidity and resistance to racemization. Its well-defined reactivity facilitates reliable deprotection and incorporation into complex peptide architectures.
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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: