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Structure of 207118-08-9
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This chiral building block features a bench-stable tert-butoxycarbonyl-protected amine paired with a trifluoromethylated aliphatic chain, enabling direct incorporation into peptide scaffolds and bioactive molecules.
(R)-2-((tert-butoxycarbonyl)amino)-4,4,4-trifluorobutanoic acid serves as a valuable chiral building block in medicinal chemistry, enabling the synthesis of fluorinated amino acid derivatives. The Boc-protected amine and trifluoromethylated aliphatic chain provide excellent functional group tolerance and stability under standard coupling conditions. Its well-defined stereochemistry facilitates asymmetric synthesis of bioactive molecules, particularly in peptidomimetics and enzyme inhibitor scaffolds where metabolic stability is enhanced by the trifluoromethyl group.
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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-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: