2-Cyano-N-(2-methoxyphenyl)acetamide, with the CAS number 63631-09-4, is an organic compound characterized by its functional groups, including a cyano group (-C≡N) and an acetamide moiety. This compound features a methoxy-substituted phenyl group, which contributes to its aromatic properties and potential reactivity. It is typically a solid at room temperature and may exhibit moderate solubility in polar organic solvents due to the presence of the methoxy group, which can engage in hydrogen bonding. The cyano group imparts notable electronic properties, making this compound of interest in various chemical syntheses and applications, particularly in pharmaceuticals and agrochemicals. Additionally, the presence of both electron-withdrawing (cyano) and electron-donating (methoxy) groups can influence its reactivity and interaction with biological systems. Safety data should be consulted for handling, as with any chemical substance, to ensure proper precautions are taken due to potential toxicity or reactivity.

2-Cyano-N-(2-methoxyphenyl)acetamide

63631-09-4: 2-Cyano-N-(2-methoxy-phenyl)-acetamide, Acetamide, 2-cyano-N-(2-methoxyphenyl)-

2-CYANO-N-(2-METHOXY-PHENYL)-ACETAMIDE

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CAS 63631-09-4: 2-Cyano-N-(2-methoxyphenyl)acetamide

2-Cyano-N-(2-methoxyphenyl)acetamide

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2-CYANO-N-(2-METHOXY-PHENYL)-ACETAMIDE

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2-Cyano-N-(2-methoxyphenyl)acetamide

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