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Structure of 203854-59-5
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(S)-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 mild coupling conditions. The side chain bears a tertiary methyl substituent, providing steric differentiation at the β-position. The compound serves as a key building block for solid-phase peptide synthesis, where its solubility and compatibility streamline sequence assembly.
(S)-2-(((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)methyl)-3-methylbutanoic acid serves as a robust chiral building block for peptide synthesis, offering high stereoselectivity and bench stability. The Fmoc group enables efficient, orthogonal protection of the amine, while the branched aliphatic side chain provides steric definition and compatibility with standard coupling protocols. Its structure facilitates clean deprotection and purification, making it well-suited for iterative solid-phase and solution-phase peptide assembly.
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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: