2-Amino-4-methoxybenzonitrile, with the CAS number 38487-85-3, is an organic compound characterized by the presence of an amino group (-NH2), a methoxy group (-OCH3), and a nitrile group (-CN) attached to a benzene ring. This compound typically appears as a solid at room temperature and is soluble in polar organic solvents due to its functional groups. The amino group can participate in hydrogen bonding, enhancing its solubility in water compared to non-polar compounds. The methoxy group contributes to the compound's electron-donating properties, which can influence its reactivity and interaction with other chemical species. Additionally, the nitrile group is known for its ability to stabilize negative charges, making the compound potentially useful in various chemical reactions, including nucleophilic substitutions. 2-Amino-4-methoxybenzonitrile may find applications in pharmaceuticals, agrochemicals, and as an intermediate in organic synthesis, owing to its diverse functional groups that allow for further chemical modifications.

2-Amino-4-methoxybenzonitrile

38487-85-3: Benzonitrile, 2-Amino-4-Methoxy-

2-Amino-4-methoxybenzonitrile is a heterocyclic organic compound. It is a synthetic building block for the synthesis of pyridines and quinolones. 2-Amino-4-methoxybenzonitrile can be synthesized by condensation of methylmagnesium chloride with nitroethane in the presence of palladium acetate. The x-ray crystallography data show that this product has a trimeric structure, which is different from the monomeric form. This difference may be due to the presence of three methyl groups on the benzene ring. The crystallographic data also support the idea that 2-amino-4-methoxybenzonitrile is an analogue of diazocine, an important precursor for pharmaceuticals and dyes.

CAS 38487-85-3: 2-Amino-4-methoxybenzonitrile

2-Amino-4-methoxybenzonitrile

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2-Amino-4-methoxybenzonitrile

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2-Amino-4-methoxybenzonitrile

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2-Amino-4-methoxybenzonitrile

Ref: IN-DA00CIRA