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CAS 270065-74-2

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Boc-(S)-3-amino-4-(2-trifluoromethyl-phenyl)-butyric acid

Description:
Boc-(S)-3-amino-4-(2-trifluoromethyl-phenyl)-butyric acid is a synthetic amino acid derivative characterized by the presence of a tert-butyloxycarbonyl (Boc) protecting group on the amino group, which enhances its stability and solubility in organic solvents. This compound features a chiral center, indicated by the (S) configuration, which is crucial for its biological activity and potential applications in pharmaceuticals. The trifluoromethyl group attached to the phenyl ring contributes to the compound's lipophilicity and can influence its interaction with biological targets. The presence of the butyric acid moiety suggests potential applications in peptide synthesis and drug development, particularly in the design of compounds that modulate biological pathways. Its molecular structure allows for various functionalization possibilities, making it a versatile intermediate in organic synthesis. As with many fluorinated compounds, it may exhibit unique properties such as increased metabolic stability and altered pharmacokinetics, which are valuable in medicinal chemistry.
Formula:C16H20F3NO4
InChI:InChI=1/C16H20F3NO4/c1-15(2,3)24-14(23)20-11(9-13(21)22)8-10-6-4-5-7-12(10)16(17,18)19/h4-7,11H,8-9H2,1-3H3,(H,20,23)(H,21,22)/t11-/m0/s1
SMILES:CC(C)(C)OC(=N[C@@H](Cc1ccccc1C(F)(F)F)CC(=O)O)O
Synonyms:
  • (3S)-3-[(tert-butoxycarbonyl)amino]-4-[2-(trifluoromethyl)phenyl]butanoic acid
  • Boc-β-HoPhe(2-CF3)-OH
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