5-Fluoro-2-(2,2,2-trifluoroacetamido)benzoic acid is a fluorinated aromatic compound characterized by the presence of a benzoic acid moiety substituted with a fluorine atom and a trifluoroacetamido group. This compound typically exhibits a solid state at room temperature and is soluble in polar organic solvents due to the presence of the carboxylic acid functional group. The trifluoroacetamido group enhances its lipophilicity and may influence its biological activity, making it of interest in pharmaceutical research. The fluorine atoms contribute to the compound's unique electronic properties, potentially affecting its reactivity and interaction with biological targets. Additionally, the presence of multiple fluorine atoms can enhance metabolic stability and alter the pharmacokinetics of the compound. As with many fluorinated compounds, it may exhibit distinct physical and chemical properties compared to its non-fluorinated analogs, including increased lipophilicity and altered hydrogen bonding capabilities. Safety and handling precautions should be observed due to the potential toxicity associated with fluorinated compounds.

5-fluoro-2-(2,2,2-trifluoroacetamido)benzoic acid

49579-59-1: 5-Fluoro-2-(2,2,2-trifluoroacetamido)benzoic acid is a fluorinated aromatic compound characterized by the presence of a benzoic acid moiety substituted with a fluorine atom and a trifluoroacetamido group. This compound typically exhibits a solid state at room temperature and is soluble in polar organic solvents due to the presence of the carboxylic acid functional group. The trifluoroacetamido group enhances its lipophilicity and may influence its biological activity, making it of interest in pharmaceutical research. The fluorine atoms contribute to the compound's unique electronic properties, potentially affecting its reactivity and interaction with biological targets. Additionally, the presence of multiple fluorine atoms can enhance metabolic stability and alter the pharmacokinetics of the compound. As with many fluorinated compounds, it may exhibit distinct physical and chemical properties compared to its non-fluorinated analogs, including increased lipophilicity and altered hydrogen bonding capabilities. Safety and handling precautions should be observed due to the potential toxicity associated with fluorinated compounds.

CAS 49579-59-1

5-fluoro-2-(2,2,2-trifluoroacetamido)benzoic acid

5-Fluoro-2-(trifluoroacetamido)benzoic acid

Ref: 3D-ZBA57959