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*For research and further manufacturing use only, not for direct human use.
Structure of 1496564-27-2
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Fmoc-Tyr(CF2H)-OH features a trifluoromethyl-substituted tyrosine residue with enhanced metabolic stability and increased lipophilicity. This fluorinated analog integrates seamlessly into peptide synthesis workflows, offering improved membrane permeability and resistance to oxidative degradation under standard conditions.
Fmoc-Tyr(CF₂H)-OH serves as a valuable building block in peptide synthesis, offering enhanced metabolic stability through the trifluoromethyl substitution on the tyrosine side chain. The Fmoc group enables efficient orthogonal protection for N-terminal amine control during solid-phase peptide synthesis. This derivative exhibits robust bench stability, facilitates straightforward purification, and maintains compatibility with standard coupling protocols, making it particularly useful for constructing bioactive peptides and peptidomimetics requiring improved resistance to oxidative degradation.
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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 : H315-H319
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Precautionary Statements : P264-P280-P302+P352-P362
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Lot numbers can be found on the outside label of a product: