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Structure of 173054-11-0
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Boc-D-(4-Fmoc)-aminophenylalanine features a protected D-amino acid scaffold with a fluorinated methoxy carbonyl group at the para position of the phenyl ring. This electron-deficient aromatic moiety enhances stability and facilitates orthogonal deprotection in peptide synthesis workflows. The Boc group enables straightforward N-terminal protection, while the Fmoc tag supports selective removal under mild basic conditions.
Boc-D-(4-Fmoc)-aminophenylalanine serves as a key building block for the synthesis of peptide-based pharmaceuticals and bioconjugates. The Fmoc group enables orthogonal protection in solid-phase peptide synthesis, while the Boc moiety provides additional stability and selective deprotection. Its phenylalanine backbone offers structural rigidity and favorable hydrophobic character, facilitating integration into complex peptide scaffolds with minimal side-reaction complications.
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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: