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Structure of 857478-30-9
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(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-methylbutanoic acid is a chiral amino acid derivative featuring a fluorenylmethoxycarbonyl (Fmoc) protecting group. This robust, bench-stable moiety enables efficient incorporation into peptide chains during solid-phase synthesis, offering high coupling yields and compatibility with standard deprotection protocols.
(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-methylbutanoic acid serves as a robust chiral building block for peptide synthesis, offering enhanced stereochemical control and stability under standard coupling conditions. The Fmoc group enables convenient deprotection with mild base, while the branched aliphatic side chain provides steric differentiation useful in constrained peptide design. Its bench-stable nature and clean purification profile facilitate efficient incorporation into complex sequences.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: