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Structure of 199006-54-7
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Fmoc-Phe(4-Me)-OH is a sterically hindered, bench-stable amino acid derivative featuring a para-methyl group that enhances hydrophobicity and metabolic stability. This modification improves incorporation efficiency in peptide synthesis and supports the construction of biologically active sequences with enhanced membrane permeability.
Fmoc-Phe(4-Me)-OH serves as a valuable building block in peptide synthesis, offering enhanced hydrophobicity and steric bulk via the 4-methyl substitution on the phenyl ring. The Fmoc group enables efficient base-labile protection for N-terminal amine control, while the side chain remains inert under standard coupling conditions. This derivative facilitates incorporation of tyrosine-like motifs with improved metabolic stability and is well-suited for solid-phase peptide synthesis workflows requiring robust handling and high-purity product isolation.
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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: