2-Amino-3,3,3-trifluoro-2-methylpropanoic acid, also known by its CAS number 422-23-1, is an amino acid derivative characterized by the presence of a trifluoromethyl group and a methyl group on its propanoic acid backbone. This compound features an amino group (-NH2) and a carboxylic acid group (-COOH), which are typical functional groups found in amino acids. The trifluoromethyl group contributes to its unique chemical properties, including increased lipophilicity and potential biological activity. The presence of fluorine atoms can enhance the stability and reactivity of the molecule, making it of interest in various fields, including medicinal chemistry and materials science. The compound is typically a white crystalline solid at room temperature and is soluble in polar solvents. Its unique structure allows for potential applications in drug design and synthesis, particularly in the development of fluorinated pharmaceuticals. As with many fluorinated compounds, it may exhibit distinct metabolic pathways and biological interactions compared to its non-fluorinated counterparts.

2-amino-3,3,3-trifluoro-2-methyl-propanoic acid

422-23-1: 2-Amino-3,3,3-trifluoro-2-methylpropanoic acid, also known by its CAS number 422-23-1, is an amino acid derivative characterized by the presence of a trifluoromethyl group and a methyl group on its propanoic acid backbone. This compound features an amino group (-NH2) and a carboxylic acid group (-COOH), which are typical functional groups found in amino acids. The trifluoromethyl group contributes to its unique chemical properties, including increased lipophilicity and potential biological activity. The presence of fluorine atoms can enhance the stability and reactivity of the molecule, making it of interest in various fields, including medicinal chemistry and materials science. The compound is typically a white crystalline solid at room temperature and is soluble in polar solvents. Its unique structure allows for potential applications in drug design and synthesis, particularly in the development of fluorinated pharmaceuticals. As with many fluorinated compounds, it may exhibit distinct metabolic pathways and biological interactions compared to its non-fluorinated counterparts.

CAS 422-23-1

2-amino-3,3,3-trifluoro-2-methyl-propanoic acid

2-Amino-3,3,3-trifluoro-2-methylpropanoic acid

Ref: 54-PC2047