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Structure of 1481642-14-1
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This fluorenylmethoxycarbonyl-protected amino acid derivative features a chiral (R)-configuration at the alpha carbon, enabling stereoselective peptide synthesis. The C-terminal ketone and methoxy group enhance solubility and reactivity in solution-phase workflows. Designed for use in solid-phase peptide coupling, this stable, bench-ready building block integrates efficiently into complex sequences.
(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-5-methoxy-5-oxopentanoic acid serves as a versatile chiral building block for peptide synthesis, enabling efficient incorporation of C-terminal α-amino-γ-keto ester motifs. The fluorenylmethoxycarbonyl (Fmoc) group provides robust protection with orthogonal cleavage under mild basic conditions, while the 5-methoxy-5-oxopentanoyl side chain offers a stable, bench-compatible platform for downstream functionalization via nucleophilic addition or reductive transformation.
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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: