2-Fluoro-4-methoxybenzonitrile is an organic compound characterized by its aromatic structure, which includes a benzene ring substituted with a fluorine atom at the second position and a methoxy group at the fourth position, along with a nitrile functional group (-C≡N) attached to the benzene. This compound typically appears as a colorless to pale yellow solid or liquid, depending on its physical state at room temperature. It is known for its moderate polarity due to the presence of the nitrile and methoxy groups, which can influence its solubility in various organic solvents. The fluorine atom contributes to its reactivity and can affect the compound's electronic properties, making it useful in various chemical syntheses and applications, including pharmaceuticals and agrochemicals. Additionally, 2-Fluoro-4-methoxybenzonitrile may exhibit specific biological activities, which can be explored in medicinal chemistry. Safety data should be consulted for handling and storage, as with any chemical substance.

2-Fluoro-4-methoxybenzonitrile

94610-82-9: 3-Fluoro-4-cyanoanisole, Benzonitrile, 2-fluoro-4-methoxy-, 2-Fluoro-4-methoxybenzonitrile

2-Fluoro-4-methoxybenzonitrile is a tetracyclic molecule with two electron deficient rings. It has intramolecular coupling, yielding four stereoisomers that show different biological activities. 2-Fluoro-4-methoxybenzonitrile is an electron deficient compound that can be synthesized by reacting dioxane with amines. It also reacts with alcohols to form ethers. This heteroaromatic compound has electron withdrawing groups that make it less stable than other heteroaromatic compounds and more reactive. 2-Fluoro-4-methoxybenzonitrile can be used in the Buchwald reaction to produce aryl chlorides from alkyl halides and aryl bromides.

CAS 94610-82-9: 2-Fluoro-4-methoxybenzonitrile

2-Fluoro-4-methoxybenzonitrile

Ref: 54-PC1358

2-Fluoro-4-methoxybenzonitrile

Ref: 10-F013330

2-Fluoro-4-methoxybenzonitrile

Ref: 3D-FF36936