2,3,6-Trifluorobenzamide is an aromatic compound characterized by the presence of a benzene ring substituted with three fluorine atoms and an amide functional group. The fluorine atoms are located at the 2, 3, and 6 positions of the benzene ring, which significantly influences the compound's chemical properties, including its reactivity and polarity. The presence of the amide group contributes to its ability to form hydrogen bonds, affecting its solubility in various solvents. This compound is typically a solid at room temperature and may exhibit moderate stability under standard conditions. Its fluorinated structure can enhance its biological activity and lipophilicity, making it of interest in pharmaceutical research and development. Additionally, the trifluoromethyl groups can impart unique electronic properties, potentially affecting the compound's interaction with biological targets. Safety data should be consulted for handling and exposure guidelines, as fluorinated compounds can exhibit varying degrees of toxicity and environmental impact.

2,3,6-trifluorobenzamide

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2,3,6-Trifluorobenzamide

Benzamide, 2,3,6-trifluoro-

2,3,6-Trifluorobenzamide is a pentafluoropyridine that can be synthesized from triethylphosphine and hexafluorobenzene. It has been used in experimental studies to investigate the mechanism of action of fluoroaromatic compounds as well as their reaction with other functionalized molecules.

CAS 207986-22-9: 2,3,6-trifluorobenzamide

2,3,6-Trifluorobenzamide

Ref: 10-F008711

2,3,6-Trifluorobenzamide

Ref: 54-PC7265V

Benzamide, 2,3,6-trifluoro-

Ref: IN-DA002JEX

2,3,6-Trifluorobenzamide

Ref: 3D-FT77848