4-Methoxy-2-nitrobenzonitrile, with the CAS number 38469-83-9, is an organic compound characterized by its aromatic structure, which includes a methoxy group (-OCH₃), a nitro group (-NO₂), and a cyano group (-CN) attached to a benzene ring. This compound typically appears as a solid and is known for its pale yellow to light brown color. It is soluble in organic solvents such as ethanol and acetone but has limited solubility in water. The presence of the nitro group contributes to its potential reactivity, making it useful in various chemical syntheses, particularly in the production of pharmaceuticals and agrochemicals. Additionally, the methoxy group can influence the compound's electronic properties and reactivity, while the cyano group can participate in nucleophilic reactions. As with many nitro compounds, it is essential to handle 4-Methoxy-2-nitrobenzonitrile with care due to potential toxicity and environmental concerns. Proper safety measures should be observed when working with this substance in a laboratory setting.

4-Methoxy-2-nitrobenzonitrile

38469-83-9: Benzonitrile, 4-Methoxy-2-Nitro-

4-Methoxy-2-nitrobenzonitrile is a molecule that has been shown to inhibit the activity of the enzyme group P2. It is used as a stabilizer in dimethylformamide, and it is also an intermediate in the synthesis of anilines. 4-Methoxy-2-nitrobenzonitrile is used pharmacologically to yield hydrogen bonds with amines, which are electron deficient. The crystal system of this molecule is monoclinic, and its electron configuration is 2p6.

CAS 38469-83-9: 4-Methoxy-2-nitrobenzonitrile

4-Methoxy-2-nitrobenzonitrile

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