3-Methoxy-5-nitrobenzonitrile is an organic compound characterized by its aromatic structure, which includes a methoxy group (-OCH3) and a nitro group (-NO2) attached to a benzene ring, along with a nitrile group (-CN). The presence of these functional groups imparts distinct chemical properties to the compound. The methoxy group is an electron-donating substituent, which can influence the reactivity of the aromatic ring, while the nitro group is an electron-withdrawing group, enhancing the compound's electrophilic character. This compound is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. It is often used in synthetic organic chemistry as an intermediate in the production of pharmaceuticals, agrochemicals, and other fine chemicals. Safety data indicates that it should be handled with care, as it may pose health risks upon exposure. Overall, 3-Methoxy-5-nitrobenzonitrile is a valuable compound in chemical synthesis, with applications stemming from its unique structural features.

3-Methoxy-5-nitrobenzonitrile

33224-19-0: Benzonitrile, 3-methoxy-5-nitro-, 3-Methoxy-5-nitrobenzonitrile

3-methoxy-5-nitrobenzonitrile

3-Methoxy-5-Nitrobenzonitrile is a natural amino acid that is synthesized by the enzyme 3,5-dinitrobenzoic acid. It is an efficient and easy to synthesize intermediate in organic chemistry. This compound has been used in the synthesis of 3-methoxy-5-nitrobenzoic acid, which is used as a precursor for other pharmaceuticals.

CAS 33224-19-0: 3-Methoxy-5-nitrobenzonitrile

3-methoxy-5-nitrobenzonitrile

Ref: IN-DA00CKQA

3-methoxy-5-nitrobenzonitrile

Ref: 54-OR910730

3-Methoxy-5-Nitrobenzonitrile

Ref: 3D-FM76219

3-Methoxy-5-nitrobenzonitrile

Ref: 10-F236524