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Structure of 203854-58-4
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(S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-methylpropanoic acid is a chiral building block featuring a fluorenylmethoxycarbonyl (Fmoc) protected amino group and a branched aliphatic side chain. This configuration enables efficient incorporation into peptide synthesis workflows, offering excellent solubility and stability under standard coupling conditions.
(S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-methylpropanoic acid serves as a robust chiral building block for peptide synthesis, enabling efficient N-terminal protection of amino acids. The Fmoc group offers high stability under basic conditions and facilitates mild deprotection with piperidine, ensuring compatibility with diverse coupling protocols. Its branched aliphatic side chain enhances solubility and reduces aggregation during solid-phase synthesis, while the stereogenic center ensures precise stereochemical control in target molecule 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: