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Structure of 460751-66-0
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(S)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-3-(5-bromo-1H-indol-3-yl)propanoic acid is a bench-stable, moisture-tolerant chiral building block featuring a protected amino acid backbone with a sterically hindered fluorenylmethoxycarbonyl (Fmoc) group. This indole-containing derivative integrates readily into peptide synthesis workflows, delivering high coupling efficiency and enabling the incorporation of biologically active indolic motifs into complex sequences.
(S)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-3-(5-bromo-1H-indol-3-yl)propanoic acid serves as a key chiral building block for the synthesis of biologically active peptides and peptidomimetics. The fluorenylmethoxycarbonyl (Fmoc) group provides excellent stability and ease of removal under mild basic conditions, while the 5-bromoindole moiety offers a versatile handle for further functionalization via cross-coupling reactions. This compound exhibits high bench stability and facilitates efficient purification, making it well-suited for solid-phase peptide synthesis and medicinal chemistry applications.
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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-H312-H332
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P501
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Lot numbers can be found on the outside label of a product: