(2R)-2-ammonio-4,4,4-trifluorobutanoate, also known as L-2-amino-4,4,4-trifluorobutanoic acid, is an amino acid derivative characterized by the presence of a trifluoromethyl group, which significantly influences its chemical properties. This compound features a chiral center, making it optically active, and it exists predominantly in its zwitterionic form at physiological pH, possessing both a positively charged ammonium group and a negatively charged carboxylate group. The trifluoromethyl substituents enhance its hydrophobicity and can affect its interactions with biological systems, potentially influencing its role in biochemical pathways. The presence of fluorine atoms can also impart unique reactivity and stability characteristics compared to non-fluorinated analogs. This compound is of interest in various fields, including medicinal chemistry and materials science, due to its potential applications in drug design and as a building block for fluorinated compounds. Its solubility in polar solvents and stability under a range of conditions make it a versatile substance for research and industrial applications.

(2R)-2-ammonio-4,4,4-trifluorobutanoate

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CAS 15960-05-1: (2R)-2-ammonio-4,4,4-trifluorobutanoate

Butanoic acid, 2-amino-4,4,4-trifluoro-, (2S)-

Ref: IN-DA001R83

(S)-2-amino-4,4,4-trifluoro-butyric acid hydrochloride

Ref: 10-F521327

(S)-2-Amino-4,4,4-trifluorobutanoic acid

Ref: 10-F618252