2-(Difluoromethoxy)-6-fluorobenzene-1-carbothioamide is a chemical compound characterized by its unique structure, which includes a benzene ring substituted with both difluoromethoxy and fluorine groups, as well as a carbothioamide functional group. The presence of the difluoromethoxy group contributes to its potential reactivity and solubility properties, while the fluorine atoms can enhance its biological activity and lipophilicity. The carbothioamide moiety may impart specific chemical reactivity, particularly in nucleophilic reactions. This compound is likely to exhibit polar characteristics due to the electronegative fluorine and oxygen atoms, influencing its interactions in various chemical environments. Additionally, the presence of multiple fluorine atoms can affect the compound's stability and volatility. As with many fluorinated compounds, it may have applications in pharmaceuticals or agrochemicals, where fluorine substitution is known to enhance metabolic stability and bioactivity. Safety and handling precautions should be observed due to the potential toxicity associated with fluorinated compounds.

2-(difluoromethoxy)-6-fluorobenzene-1-carbothioamide

1155138-78-5: 2-(Difluoromethoxy)-6-fluorobenzene-1-carbothioamide is a chemical compound characterized by its unique structure, which includes a benzene ring substituted with both difluoromethoxy and fluorine groups, as well as a carbothioamide functional group. The presence of the difluoromethoxy group contributes to its potential reactivity and solubility properties, while the fluorine atoms can enhance its biological activity and lipophilicity. The carbothioamide moiety may impart specific chemical reactivity, particularly in nucleophilic reactions. This compound is likely to exhibit polar characteristics due to the electronegative fluorine and oxygen atoms, influencing its interactions in various chemical environments. Additionally, the presence of multiple fluorine atoms can affect the compound's stability and volatility. As with many fluorinated compounds, it may have applications in pharmaceuticals or agrochemicals, where fluorine substitution is known to enhance metabolic stability and bioactivity. Safety and handling precautions should be observed due to the potential toxicity associated with fluorinated compounds.

CAS 1155138-78-5

2-(difluoromethoxy)-6-fluorobenzene-1-carbothioamide

2-(Difluoromethoxy)-6-fluorobenzene-1-carbothioamide

Ref: 3D-FWB13878