(2,6-Dimethylphenyl)-(4-methoxyphenyl)methanone, also known by its CAS number 52629-41-1, is an organic compound characterized by its ketone functional group, specifically a methanone structure where a carbonyl group is bonded to two distinct aromatic rings. The presence of the 2,6-dimethylphenyl group contributes to its hydrophobic nature and potential steric hindrance, while the 4-methoxyphenyl group introduces an electron-donating methoxy substituent, which can influence the compound's reactivity and stability. This compound is typically solid at room temperature and may exhibit moderate solubility in organic solvents. Its molecular structure suggests potential applications in organic synthesis, particularly in the development of pharmaceuticals or agrochemicals, due to the reactivity of the carbonyl group. Additionally, the presence of multiple aromatic rings may impart interesting photophysical properties, making it a candidate for studies in materials science or dye chemistry. As with many organic compounds, safety data should be consulted for handling and usage.

(2,6-dimethylphenyl)-(4-methoxyphenyl)methanone

52629-41-1: (2,6-Dimethylphenyl)-(4-methoxyphenyl)methanone, also known by its CAS number 52629-41-1, is an organic compound characterized by its ketone functional group, specifically a methanone structure where a carbonyl group is bonded to two distinct aromatic rings. The presence of the 2,6-dimethylphenyl group contributes to its hydrophobic nature and potential steric hindrance, while the 4-methoxyphenyl group introduces an electron-donating methoxy substituent, which can influence the compound's reactivity and stability. This compound is typically solid at room temperature and may exhibit moderate solubility in organic solvents. Its molecular structure suggests potential applications in organic synthesis, particularly in the development of pharmaceuticals or agrochemicals, due to the reactivity of the carbonyl group. Additionally, the presence of multiple aromatic rings may impart interesting photophysical properties, making it a candidate for studies in materials science or dye chemistry. As with many organic compounds, safety data should be consulted for handling and usage.

CAS 52629-41-1

(2,6-dimethylphenyl)-(4-methoxyphenyl)methanone

2,6-dimethyl-4′-methoxybenzophenone

Ref: 10-F201592