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Structure of 460751-70-6
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(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(2-methyl-1H-indol-3-yl)propanoic acid features a chiral α-amino acid scaffold bearing a fluorenylmethoxycarbonyl (Fmoc) protecting group and a sterically influenced 2-methylindole side chain. This configuration enables direct incorporation into peptide synthesis workflows, where the Fmoc moiety facilitates efficient stepwise coupling under standard conditions. The indole functionality provides a rigid, electron-rich aromatic handle suitable for downstream derivatization or structural probing in bioactive peptide design.
(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(2-methyl-1H-indol-3-yl)propanoic acid serves as a robust chiral building block for peptide synthesis, enabling efficient incorporation of the 2-methylindole moiety into bioactive scaffolds. The Fmoc group provides orthogonal protection and facile removal under mild basic conditions, while the sterically defined (S)-configuration ensures high diastereoselectivity in coupling reactions. Its bench-stable nature and compatibility with standard amino acid coupling protocols make it ideal 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: