4-Fluorophenyl chlorothionoformate is a chemical compound characterized by its unique functional groups and structure. It features a fluorine atom attached to a phenyl ring, which contributes to its reactivity and potential applications in organic synthesis. The presence of the chlorothionoformate group indicates that it can act as a thiocarbonate, making it useful in various chemical reactions, particularly in the formation of thioesters and in the synthesis of other organosulfur compounds. This compound is typically a colorless to pale yellow liquid, exhibiting moderate volatility and solubility in organic solvents. It is important to handle 4-fluorophenyl chlorothionoformate with care, as it may be toxic and can cause irritation upon contact with skin or mucous membranes. Additionally, it may undergo hydrolysis in the presence of moisture, leading to the formation of corresponding thiols and hydrochloric acid. As with many organofluorine compounds, its unique properties make it of interest in pharmaceuticals and agrochemicals, where fluorine can enhance biological activity and stability.

4-fluorophenyl chlorothionoformate

42908-73-6: 4-Fluorophenyl chlorothionoformate is a chemical compound characterized by its unique functional groups and structure. It features a fluorine atom attached to a phenyl ring, which contributes to its reactivity and potential applications in organic synthesis. The presence of the chlorothionoformate group indicates that it can act as a thiocarbonate, making it useful in various chemical reactions, particularly in the formation of thioesters and in the synthesis of other organosulfur compounds. This compound is typically a colorless to pale yellow liquid, exhibiting moderate volatility and solubility in organic solvents. It is important to handle 4-fluorophenyl chlorothionoformate with care, as it may be toxic and can cause irritation upon contact with skin or mucous membranes. Additionally, it may undergo hydrolysis in the presence of moisture, leading to the formation of corresponding thiols and hydrochloric acid. As with many organofluorine compounds, its unique properties make it of interest in pharmaceuticals and agrochemicals, where fluorine can enhance biological activity and stability.

CAS 42908-73-6

4-fluorophenyl chlorothionoformate

4-Fluorophenyl Chlorothionoformate

Ref: 3B-F0365

4-Fluorophenyl Chlorothionoformate

Ref: IN-DA003LFX

4-Fluorophenyl chlorothionoformate

Ref: 54-PC906433