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: O-(4-fluorophenyl) chlorothiocarbonate, 4-Fluorophenyl Chlorothioformate

Carbonochloridothioic Acid O-(4-Fluorophenyl) Ester is a research chemical that has various characteristics and applications. It is a fatty acid derivative that can be used in the synthesis of phytoestrogens, which are plant-derived compounds that mimic the effects of estrogen in the body. Additionally, it can be utilized in the production of ergosterol, a sterol found in fungi and yeast.

This compound also has potential applications in antibody research. It can be used as a reagent to modify antibodies, allowing for improved detection or binding to specific targets. Furthermore, Carbonochloridothioic Acid O-(4-Fluorophenyl) Ester has been studied for its electrolyte properties and its ability to form hydrogen bonds with other molecules.

In addition to its research applications, this compound has shown antibiotic activity against certain bacterial strains. It binds to specific proteins in bacteria, inhibiting their growth and replication. This makes it

CAS 42908-73-6: 4-fluorophenyl chlorothionoformate

Carbonochloridothioic Acid O-(4-Fluorophenyl) Ester

Ref: 3D-FC92471

4-Fluorophenyl Chlorothionoformate

Ref: 3B-F0365

4-FLUOROPHENYL CHLOROTHIONOFORMATE

Ref: IN-DA003LFX

4-Fluorophenyl chlorothionoformate

Ref: 54-PC906433