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CAS 242475-26-9

:

(2S)-amino[3-(trifluoromethyl)phenyl]ethanoic acid

Description:
(2S)-Amino[3-(trifluoromethyl)phenyl]ethanoic acid, also known as a specific amino acid derivative, is characterized by its structural features that include an amino group, a carboxylic acid group, and a phenyl ring substituted with a trifluoromethyl group. This compound is a chiral molecule, with the (2S) designation indicating its specific stereochemistry. The presence of the trifluoromethyl group enhances its lipophilicity and can influence its biological activity, making it of interest in pharmaceutical research. The amino acid structure allows it to participate in various biochemical processes, potentially acting as a building block for peptides or influencing protein interactions. Its CAS number, 242475-26-9, is a unique identifier that facilitates the tracking and study of this compound in scientific literature and databases. Overall, this substance exhibits properties typical of amino acids, such as solubility in water and the ability to form hydrogen bonds, while also possessing unique characteristics due to the trifluoromethyl substitution.
Formula:C9H8F3NO2
InChI:InChI=1/C9H8F3NO2/c10-9(11,12)6-3-1-2-5(4-6)7(13)8(14)15/h1-4,7H,13H2,(H,14,15)/t7-/m0/s1
SMILES:c1cc(cc(c1)C(F)(F)F)[C@@H](C(=O)O)N
Synonyms:
  • Amino[3-(Trifluoromethyl)Phenyl]Acetic Acid
  • Benzeneacetic acid, alpha-amino-3-(trifluoromethyl)-
  • (2R)-amino[3-(trifluoromethyl)phenyl]ethanoic acid
  • 3-(TrifluoroMethyl)-DL-phenylglycine
  • 2-[3-(Trifluoromethyl)phenyl]glycine
  • Benzeneacetic acid, α-amino-3-(trifluoromethyl)-
  • Benzeneacetic acid, α-amino-3-(trifluoromethyl)Ethanone, 1-(2-fluoro-5-nitrophenyl)-
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