2,2,2-Trifluoro-N-[3-(trifluoromethyl)phenyl]acetamide, with the CAS number 2946-73-8, is a synthetic organic compound characterized by its unique trifluoromethyl groups, which significantly influence its chemical properties. This compound features a central acetamide structure, where the presence of three fluorine atoms on both the acetamide and the phenyl ring enhances its lipophilicity and stability. The trifluoromethyl groups contribute to its potential as a bioactive molecule, often exhibiting interesting pharmacological properties. Additionally, the compound is likely to be solid at room temperature and may have a relatively high melting point due to strong intermolecular interactions. Its polar nature, attributed to the amide functional group, allows for potential solubility in polar solvents. The presence of multiple fluorine atoms also suggests that it may exhibit unique reactivity patterns, making it of interest in various chemical applications, including pharmaceuticals and agrochemicals. Safety data should be consulted for handling, as fluorinated compounds can pose specific health and environmental risks.

2,2,2-trifluoro-N-[3-(trifluoromethyl)phenyl]acetamide

2946-73-8: 2,2,2-Trifluoro-N-[3-(trifluoromethyl)phenyl]acetamide, with the CAS number 2946-73-8, is a synthetic organic compound characterized by its unique trifluoromethyl groups, which significantly influence its chemical properties. This compound features a central acetamide structure, where the presence of three fluorine atoms on both the acetamide and the phenyl ring enhances its lipophilicity and stability. The trifluoromethyl groups contribute to its potential as a bioactive molecule, often exhibiting interesting pharmacological properties. Additionally, the compound is likely to be solid at room temperature and may have a relatively high melting point due to strong intermolecular interactions. Its polar nature, attributed to the amide functional group, allows for potential solubility in polar solvents. The presence of multiple fluorine atoms also suggests that it may exhibit unique reactivity patterns, making it of interest in various chemical applications, including pharmaceuticals and agrochemicals. Safety data should be consulted for handling, as fluorinated compounds can pose specific health and environmental risks.

AcetaMide, 2,2,2-trifluoro-N-[3-(trifluoroMethyl)phenyl]-

2,2,2-Trifluoro-N-[3-(trifluoromethyl)phenyl]acetamide

CAS 2946-73-8

2,2,2-trifluoro-N-[3-(trifluoromethyl)phenyl]acetamide

AcetaMide, 2,2,2-trifluoro-N-[3-(trifluoroMethyl)phenyl]-

Ref: IN-DA002YFX

2,2,2-Trifluoro-N-[3-(trifluoromethyl)phenyl]acetamide

Ref: 54-PC27980