3-(2-Methylphenyl)-3-oxopropanenitrile, with the CAS number 35276-81-4, is an organic compound characterized by its functional groups, including a nitrile and a ketone. This compound features a propanone backbone substituted with a 2-methylphenyl group, which contributes to its aromatic properties. The presence of the nitrile group (-C≡N) indicates that it can participate in various chemical reactions, such as nucleophilic additions or hydrolysis, making it versatile in synthetic organic chemistry. The compound is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. Its molecular structure suggests potential applications in pharmaceuticals, agrochemicals, or as an intermediate in organic synthesis. Additionally, the compound's reactivity and stability can be influenced by the electronic effects of the methyl and phenyl substituents, which may affect its behavior in chemical reactions. Safety data should be consulted for handling and storage, as with any chemical substance.

3-(2-methylphenyl)-3-oxopropanenitrile

35276-81-4: Benzenepropanenitrile, 2-Methyl-Beta-Oxo-

2-Methylbenzoylacetonitrile is a reactive compound that can undergo cyclization and oxidation reactions. It can be used in the synthesis of other compounds, such as acetophenone. The postulated mechanism of this reaction is shown below:

2-methylbenzoylacetonitrile + tert-butyl hydroperoxide → 2-methylbenzoic acid + tert-butyl alcohol + hydrogen peroxide 

2-methylbenzoic acid + thiourea → 2-methylbenzoyl amide 

2-methylbenzoyl amide + methylene → 2-(2-methylphenyl)acetamide 

Hydroperoxide (HOOH) + methylene → acetic acid 

This reaction forms an acetic acid molecule and a methylene molecule.

CAS 35276-81-4: 3-(2-methylphenyl)-3-oxopropanenitrile

2-Methylbenzoylacetonitrile

Ref: 3D-FM54255

3-(2-Methylphenyl)-3-oxopropanenitrile

Ref: 54-OR909663

2-Methylbenzoylacetonitrile

Ref: 10-F206988

3-Oxo-3-(o-tolyl)propanenitrile

Ref: IN-DA007DXJ