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Structure of 486460-09-7
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(R)-2-((tert-Butoxycarbonyl)amino)-3-(2,4,5-trifluorophenyl)propanoic acid is a chiral building block featuring a trifluorophenyl moiety and a protected amino group. This bench-stable, moisture-tolerant derivative enables direct incorporation into peptide synthesis workflows. The electron-deficient aryl ring enhances reactivity in coupling reactions, while the (R)-configuration ensures stereochemical fidelity in target molecule construction.
(R)-2-((tert-Butoxycarbonyl)amino)-3-(2,4,5-trifluorophenyl)propanoic acid serves as a valuable chiral building block in medicinal chemistry, enabling the synthesis of peptide-like scaffolds and bioactive molecules. The tert-butyl carbamate (Boc) group provides excellent stability and orthogonal deprotection under mild acidic conditions, while the 2,4,5-trifluorophenyl moiety enhances metabolic stability and modulates electronic properties. This compound facilitates efficient coupling reactions and is well-suited for solid-phase and solution-phase synthesis workflows.
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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: