1-(2,6-Dichlorophenyl)-3-(p-tolyl)propan-1-one, identified by its CAS number 898769-46-5, is an organic compound that belongs to the class of ketones. This substance features a propanone backbone with two distinct aromatic substituents: a dichlorophenyl group and a p-tolyl group. The presence of chlorine atoms on the phenyl ring enhances its lipophilicity and may influence its biological activity. The compound is typically characterized by its solid state at room temperature and exhibits a specific melting point and boiling point, which are influenced by its molecular structure. Its chemical properties include reactivity typical of ketones, such as undergoing nucleophilic addition reactions. Additionally, it may exhibit interesting pharmacological properties, making it a subject of interest in medicinal chemistry. Safety data should be consulted for handling, as with many organic compounds, it may pose health risks if not managed properly. Overall, this compound's unique structure and functional groups contribute to its potential applications in various fields, including pharmaceuticals and agrochemicals.

1-(2,6-dichlorophenyl)-3-(p-tolyl)propan-1-one

898769-46-5: 1-(2,6-Dichlorophenyl)-3-(p-tolyl)propan-1-one, identified by its CAS number 898769-46-5, is an organic compound that belongs to the class of ketones. This substance features a propanone backbone with two distinct aromatic substituents: a dichlorophenyl group and a p-tolyl group. The presence of chlorine atoms on the phenyl ring enhances its lipophilicity and may influence its biological activity. The compound is typically characterized by its solid state at room temperature and exhibits a specific melting point and boiling point, which are influenced by its molecular structure. Its chemical properties include reactivity typical of ketones, such as undergoing nucleophilic addition reactions. Additionally, it may exhibit interesting pharmacological properties, making it a subject of interest in medicinal chemistry. Safety data should be consulted for handling, as with many organic compounds, it may pose health risks if not managed properly. Overall, this compound's unique structure and functional groups contribute to its potential applications in various fields, including pharmaceuticals and agrochemicals.

CAS 898769-46-5

1-(2,6-dichlorophenyl)-3-(p-tolyl)propan-1-one

2′,6′-dichloro-3-(4-methylphenyl)propiophenone

Ref: 10-F205771