2-Ethyl-6-methylbenzonitrile is an aromatic compound characterized by a benzene ring substituted with both an ethyl group and a methyl group, along with a nitrile functional group. Its molecular structure features a cyano group (-C≡N) attached to the benzene ring, which contributes to its chemical reactivity and polarity. This compound typically appears as a colorless to pale yellow liquid or solid, depending on the temperature and purity. It is known for its relatively low volatility and moderate solubility in organic solvents, making it useful in various chemical applications. The presence of the nitrile group imparts certain properties, such as increased dipole moment and potential for hydrogen bonding, which can influence its behavior in chemical reactions. Additionally, 2-Ethyl-6-methylbenzonitrile may exhibit biological activity, making it of interest in pharmaceutical and agrochemical research. Safety data should be consulted for handling and exposure guidelines, as with any chemical substance.

2-Ethyl-6-methylbenzonitrile

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2-Ethyl-6-methylbenzonitrile is a potent inhibitor of the enzyme alkoxycarbonylation, which is used in the synthesis of pharmaceuticals and other organic compounds. This reversible inhibitor binds to palladium and forms a covalent bond with it, forming a complex that is catalyzed by oxygen. This irreversible inhibition leads to an accumulation of 2-ethyl-6-methylbenzonitrile and prevents the production of the desired product. 2-Ethyl-6-methylbenzonitrile is more potent than its corresponding ethyl analogue because it has a greater affinity for palladium.

CAS 95881-22-4: 2-Ethyl-6-methylbenzonitrile

2-Ethyl-6-methylbenzonitrile

Ref: 3D-VDA88122

2-Ethyl-6-methylbenzonitrile

Ref: 54-OR30118