(4-Fluorobenzyl)phenyl sulfide, with the CAS number 351-66-6, is an organic compound characterized by the presence of a fluorobenzyl group and a phenyl sulfide moiety. This compound typically exhibits a molecular structure that includes a sulfur atom bonded to a phenyl group and a 4-fluorobenzyl group, which contributes to its unique chemical properties. It is generally a colorless to pale yellow liquid or solid, depending on the temperature and purity. The presence of the fluorine atom enhances its lipophilicity and can influence its reactivity and interaction with biological systems. (4-Fluorobenzyl)phenyl sulfide may be utilized in various chemical syntheses and research applications, particularly in the fields of medicinal chemistry and materials science. Its properties, such as solubility, boiling point, and stability, can vary based on environmental conditions and the presence of other functional groups. As with many organosulfur compounds, it may exhibit specific biological activities, making it of interest for further study in pharmacology and toxicology.

(4-fluorobenzyl)phenyl sulfide

351-66-6: (4-Fluorobenzyl)phenyl sulfide, with the CAS number 351-66-6, is an organic compound characterized by the presence of a fluorobenzyl group and a phenyl sulfide moiety. This compound typically exhibits a molecular structure that includes a sulfur atom bonded to a phenyl group and a 4-fluorobenzyl group, which contributes to its unique chemical properties. It is generally a colorless to pale yellow liquid or solid, depending on the temperature and purity. The presence of the fluorine atom enhances its lipophilicity and can influence its reactivity and interaction with biological systems. (4-Fluorobenzyl)phenyl sulfide may be utilized in various chemical syntheses and research applications, particularly in the fields of medicinal chemistry and materials science. Its properties, such as solubility, boiling point, and stability, can vary based on environmental conditions and the presence of other functional groups. As with many organosulfur compounds, it may exhibit specific biological activities, making it of interest for further study in pharmacology and toxicology.

CAS 351-66-6

(4-fluorobenzyl)phenyl sulfide

4-Fluorobenzyl phenyl sulphide

Ref: 54-PC3721TM

1-Fluoro-4-(phenylsulfanylmethyl)benzene

Ref: 10-F006208