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Structure of 176504-01-1
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This fluorenylmethoxycarbonyl-protected amino acid derivative features a benzyl side chain bearing a carboxylic acid group, enabling direct incorporation into peptide synthesis workflows. The C-terminal functionality integrates seamlessly with standard coupling protocols, while the fluoren-9-ylmethoxycarbonyl (Fmoc) moiety ensures orthogonal protection and high stability under basic conditions.
2-(4-(((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)methyl)phenyl)acetic acid serves as a versatile building block for peptide and peptidomimetic synthesis, enabling efficient incorporation of aromatic side chains with enhanced solubility and stability. The Fmoc group provides orthogonal protection for primary amines, facilitating automated solid-phase peptide synthesis. Its benzylic acetic acid functionality supports diverse downstream modifications, including amidation and esterification, while the fluorenylmethoxycarbonyl moiety ensures clean deprotection under mild basic conditions.
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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: