4,4-Difluoro-3-oxobutanenitrile is a chemical compound characterized by its unique structure, which includes a nitrile functional group and two fluorine atoms attached to the butanone backbone. This compound features a carbonyl group (C=O) adjacent to the nitrile (C≡N), contributing to its reactivity and potential applications in organic synthesis. The presence of fluorine atoms enhances its electrophilic character, making it useful in various chemical reactions, including nucleophilic additions. The compound is typically a colorless to pale yellow liquid or solid, depending on its state at room temperature. It is important to handle this substance with care, as it may pose health risks if inhaled or ingested, and appropriate safety measures should be taken during its use in laboratory settings. Additionally, its unique properties may make it a candidate for research in pharmaceuticals or agrochemicals, where fluorinated compounds often exhibit enhanced biological activity. As with any chemical, understanding its reactivity and stability under various conditions is crucial for safe and effective application.

4,4-difluoro-3-oxobutanenitrile

1261289-79-5: 4,4-Difluoro-3-oxobutanenitrile is a chemical compound characterized by its unique structure, which includes a nitrile functional group and two fluorine atoms attached to the butanone backbone. This compound features a carbonyl group (C=O) adjacent to the nitrile (C≡N), contributing to its reactivity and potential applications in organic synthesis. The presence of fluorine atoms enhances its electrophilic character, making it useful in various chemical reactions, including nucleophilic additions. The compound is typically a colorless to pale yellow liquid or solid, depending on its state at room temperature. It is important to handle this substance with care, as it may pose health risks if inhaled or ingested, and appropriate safety measures should be taken during its use in laboratory settings. Additionally, its unique properties may make it a candidate for research in pharmaceuticals or agrochemicals, where fluorinated compounds often exhibit enhanced biological activity. As with any chemical, understanding its reactivity and stability under various conditions is crucial for safe and effective application.

CAS 1261289-79-5

4,4-difluoro-3-oxobutanenitrile

4,4-Difluoro-3-oxobutanenitrile

Ref: IN-DA00HIW6