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Structure of 517905-87-2
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Fmoc-(R)-3-amino-3-(3-trifluoromethylphenyl)-propionic acid is a sterically hindered, bench-stable amino acid derivative featuring a trifluoromethyl-substituted aromatic ring. This electron-deficient phenyl group enhances metabolic stability and modulates lipophilicity. The Fmoc protecting group enables efficient solid-phase peptide synthesis, while the chiral (R)-configuration ensures stereochemical fidelity in sequence assembly.
Fmoc-(R)-3-amino-3-(3-trifluoromethylphenyl)-propionic acid serves as a valuable building block for peptide synthesis, enabling the incorporation of a sterically hindered, electron-deficient aromatic side chain. The Fmoc group ensures orthogonal protection for the amine, while the trifluoromethylphenyl moiety imparts enhanced metabolic stability and lipophilicity—key attributes in medicinal chemistry lead optimization. This amino acid derivative exhibits excellent bench stability, facilitates straightforward purification, and participates reliably in standard coupling protocols.
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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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: