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Structure of 587880-86-2
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This fluoren-9-ylmethoxycarbonyl-protected amino acid derivative features a chiral (2S) configuration and a dimethylamino group at the C3 position, enabling efficient incorporation into peptide chains. The robust fluorenylmethoxycarbonyl (Fmoc) moiety ensures stable protection during solid-phase synthesis, while the electron-rich aromatic system enhances solubility and compatibility with standard coupling protocols.
(2S)-3-(Dimethylamino)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)propanoic acid serves as a key chiral building block in peptide synthesis, offering high stability and compatibility with standard coupling protocols. The Fmoc-protected amine enables efficient sequential elongation, while the dimethylamino group provides enhanced solubility and facilitates purification. Its well-defined stereochemistry ensures reliable incorporation into complex peptides and peptidomimetics.
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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 : H315-H319-H335
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Precautionary Statements : P260-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P332+P313-P337+P313-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: