3-(2,4-Dimethylphenyl)-1-(2,6-dimethylphenyl)propan-1-one, with the CAS number 898794-11-1, is an organic compound that belongs to the class of ketones. It features a propanone backbone substituted with two aromatic rings, specifically dimethylphenyl groups, which contribute to its unique chemical properties. The presence of multiple methyl groups on the phenyl rings enhances its hydrophobic character and can influence its reactivity and solubility in organic solvents. This compound is typically characterized by its molecular structure, which includes a central carbonyl group (C=O) flanked by the two aromatic substituents. The compound may exhibit interesting photophysical properties, making it of interest in various applications, including organic synthesis and materials science. Additionally, due to its structural complexity, it may undergo various chemical reactions typical of ketones, such as nucleophilic addition and oxidation. Safety and handling precautions should be observed, as with many organic compounds, to mitigate any potential hazards associated with its use.

3-(2,4-dimethylphenyl)-1-(2,6-dimethylphenyl)propan-1-one

898794-11-1: 3-(2,4-Dimethylphenyl)-1-(2,6-dimethylphenyl)propan-1-one, with the CAS number 898794-11-1, is an organic compound that belongs to the class of ketones. It features a propanone backbone substituted with two aromatic rings, specifically dimethylphenyl groups, which contribute to its unique chemical properties. The presence of multiple methyl groups on the phenyl rings enhances its hydrophobic character and can influence its reactivity and solubility in organic solvents. This compound is typically characterized by its molecular structure, which includes a central carbonyl group (C=O) flanked by the two aromatic substituents. The compound may exhibit interesting photophysical properties, making it of interest in various applications, including organic synthesis and materials science. Additionally, due to its structural complexity, it may undergo various chemical reactions typical of ketones, such as nucleophilic addition and oxidation. Safety and handling precautions should be observed, as with many organic compounds, to mitigate any potential hazards associated with its use.

CAS 898794-11-1

3-(2,4-dimethylphenyl)-1-(2,6-dimethylphenyl)propan-1-one

2′,6′-dimethyl-3-(2,4-dimethylphenyl)propiophenone

Ref: 10-F206436