2,6-Difluorophenyl isothiocyanate is an organic compound characterized by the presence of both a phenyl ring and an isothiocyanate functional group. The molecular structure features two fluorine atoms positioned at the 2 and 6 positions of the phenyl ring, which significantly influences its chemical reactivity and physical properties. This compound is typically a colorless to pale yellow liquid with a pungent odor, indicative of the isothiocyanate group. It is known for its reactivity, particularly in nucleophilic substitution reactions, making it useful in various synthetic applications, including the preparation of thioureas and other nitrogen-containing compounds. Additionally, the presence of fluorine atoms can enhance the compound's lipophilicity and stability, affecting its behavior in biological systems. As with many isothiocyanates, it may exhibit biological activity, including potential antimicrobial or anticancer properties, although specific biological effects would depend on the context of its use. Proper handling and safety precautions are essential due to its potential toxicity and irritant nature.

2,6-Difluorophenyl isothiocyanate

207974-17-2: 1,3-Difluoro-2-Isocyanatobenzene

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CAS 207974-17-2: 2,6-Difluorophenyl isothiocyanate

2,6-Difluorophenyl isothiocyanate

Ref: 54-PC5347

2,6-Difluorophenyl isothiocyanate

Ref: 3D-FD98998

Benzene, 1,3-difluoro-2-isothiocyanato-

Ref: IN-DA002JEE

2,6-Difluorophenyl isothiocyanate

Ref: 10-F005374