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Structure of 204322-23-6
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Fmoc-Tpi-OH is a bench-stable, moisture-tolerant amino acid derivative featuring a trifluoromethylphenyl isoxazole side chain. This structure integrates a rigid, electron-deficient heterocycle that enhances backbone conformational control during peptide synthesis. The Fmoc group enables efficient N-terminal protection, while the hydroxyl handle supports direct coupling or derivatization. Ideal for incorporating non-natural scaffolds into bioactive peptides.
Fmoc-Tpi-OH serves as a robust building block for peptide synthesis, enabling efficient incorporation of the trifluoromethylated phenylalanine derivative Tpi into target sequences. The Fmoc group provides orthogonal protection compatible with standard coupling protocols, while the pendant trifluoromethylphenyl moiety imparts enhanced metabolic stability and modulates lipophilicity. Its bench-stable solid form facilitates handling and purification, making it well-suited for both manual and automated synthesis workflows in medicinal chemistry and peptide-based drug discovery.
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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: