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Structure of 281655-61-6
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This fluoren-9-ylmethoxycarbonyl-protected amino acid features a quinolin-3-yl side chain, enabling direct incorporation into peptide sequences via standard coupling protocols. The C-terminal carboxyl group is readily activated for amide bond formation, while the Fmoc group ensures orthogonal protection during solid-phase synthesis.
(2S)-2-([(9H-fluoren-9-ylmethoxy)carbonyl]amino)-3-(quinolin-3-yl)propanoic acid serves as a valuable chiral building block for the synthesis of peptidomimetics and bioactive heterocyclic compounds. The fluorenylmethoxycarbonyl (Fmoc) group enables efficient solid-phase peptide synthesis, while the quinolin-3-yl moiety provides a rigid, electron-deficient aromatic system suitable for metal-catalyzed coupling reactions and medicinal chemistry optimization. This compound exhibits excellent bench stability, facilitates straightforward purification, and functions reliably in standard amine protection and coupling protocols.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: