2,3-Difluoro-5-methylbenzonitrile is an organic compound characterized by its aromatic structure, which includes a benzene ring substituted with two fluorine atoms and a methyl group, along with a cyano group (-C≡N). The presence of the fluorine atoms contributes to its unique chemical properties, such as increased electronegativity and potential for enhanced reactivity compared to non-fluorinated analogs. The cyano group imparts significant polarity, making the compound useful in various chemical applications, including as an intermediate in organic synthesis and in the development of pharmaceuticals. The compound is typically a colorless to pale yellow liquid or solid, depending on its state at room temperature. Its solubility in organic solvents and limited solubility in water are typical for such aromatic nitriles. Additionally, the presence of fluorine can influence the compound's boiling and melting points, as well as its stability under various conditions. Safety data should be consulted for handling, as fluorinated compounds can exhibit toxicity and environmental persistence.

2,3-Difluoro-5-methylbenzonitrile

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CAS 1003712-18-2: 2,3-Difluoro-5-methylbenzonitrile

2,3-Difluoro-5-methylbenzonitrile

Ref: 54-PC56801

2,3-Difluoro-5-methylbenzonitrile

Ref: 3D-DQB71218

2,3-Difluoro-5-methylbenzonitrile

Ref: 10-F037169

Benzonitrile, 2,3-difluoro-5-methyl-

Ref: IN-DA0001SE