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Structure of 211637-74-0
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Fmoc-Phe(3-Me)-OH features a phenylalanine residue with a 3-methyl substitution, enhancing hydrophobicity and steric bulk. This modification improves peptide stability and membrane permeability in synthetic sequences. The Fmoc group enables efficient solid-phase peptide synthesis under standard conditions.
Fmoc-Phe(3-Me)-OH serves as a valuable building block in peptide synthesis, offering enhanced hydrophobicity and metabolic stability due to the 3-methyl substitution on the phenyl ring. The Fmoc group enables efficient base-mediated deprotection, while the side chain’s methyl group improves resistance to oxidative degradation. This derivative facilitates the incorporation of sterically hindered, lipophilic residues into therapeutic peptides with improved pharmacokinetic profiles.
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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: