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*For research and further manufacturing use only, not for direct human use.
Structure of 204260-38-8
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Fmoc-D-Phe(4-Me)-OH features a fluorophore-masked D-phenylalanine derivative with a para-methyl substituent, enabling efficient incorporation into peptide chains. The electron-donating methyl group enhances stability and modulates backbone conformation during solid-phase synthesis. This bench-stable building block facilitates the installation of D-configured aromatic residues in bioactive peptide sequences.
Fmoc-D-Phe(4-Me)-OH serves as a key building block in peptide synthesis, enabling the incorporation of D-phenylalanine with a para-methyl substituent. The Fmoc group provides orthogonal protection for amine functionality, facilitating efficient stepwise chain elongation. The 4-methylphenyl side chain enhances hydrophobicity and steric bulk, offering favorable properties for peptide stability and receptor interaction. This derivative exhibits excellent bench stability, clean coupling efficiency, and compatibility with standard purification methods, making it ideal for medicinal chemistry and peptide library development.
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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: