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CAS 167993-21-7

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Boc-L-2-Trifluoromethylphe

Description:
Boc-L-2-Trifluoromethylphenylalanine, commonly referred to as Boc-L-2-Trifluoromethylphe, is a synthetic amino acid derivative characterized by the presence of a tert-butyloxycarbonyl (Boc) protecting group and a trifluoromethyl group attached to the phenyl ring. This compound is notable for its unique electronic properties due to the trifluoromethyl group, which can influence the reactivity and stability of the molecule. The Boc group serves as a protective moiety that facilitates the synthesis of peptides by preventing unwanted reactions during coupling processes. Typically, this compound is utilized in peptide synthesis and medicinal chemistry, particularly in the development of pharmaceuticals where modifications to amino acids can enhance biological activity or selectivity. Its structure allows for potential applications in drug design, especially in targeting specific biological pathways. As with many fluorinated compounds, it may exhibit distinct solubility and lipophilicity characteristics, which can be advantageous in various chemical and biological contexts.
Formula:C15H18F3NO4
InChI:InChI=1/C15H18F3NO4/c1-14(2,3)23-13(22)19-11(12(20)21)8-9-6-4-5-7-10(9)15(16,17)18/h4-7,11H,8H2,1-3H3,(H,19,22)(H,20,21)/t11-/m1/s1
SMILES:CC(C)(C)OC(=N[C@H](Cc1ccccc1C(F)(F)F)C(=O)O)O
Synonyms:
  • Boc-L-2-Trifluoromethylphenylalanine
  • N-(tert-butoxycarbonyl)-2-(trifluoromethyl)-L-phenylalanine
  • N-(tert-butoxycarbonyl)-2-(trifluoromethyl)-D-phenylalanine
  • Boc-2-Trifluoromethyl-L-phenylalanine
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