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Structure of 198545-72-1
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Fmoc-D-Phe(3-F)-OH features a fluorinated phenyl ring at the meta position, enhancing electron-withdrawing character and metabolic stability. This derivative integrates readily into peptide chains under standard coupling conditions, offering improved solubility and reduced aggregation during synthesis. The Fmoc group enables efficient N-terminal protection and stepwise elongation in solid-phase peptide synthesis.
Fmoc-D-Phe(3-F)-OH serves as a valuable building block in peptide synthesis, offering enhanced metabolic stability and modulated hydrophobicity through the meta-fluorinated phenyl side chain. The Fmoc group enables efficient N-terminal protection for solid-phase peptide synthesis, while the D-configuration imparts resistance to enzymatic degradation. This derivative facilitates the incorporation of fluorinated aromatic residues into bioactive peptides with improved membrane permeability and target binding affinity.
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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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: