1-(3,4-Dichlorophenyl)-3-(2,3-dimethylphenyl)propan-1-one, with the CAS number 898793-29-8, is an organic compound characterized by its ketone functional group, specifically a propanone structure. This compound features a propan-1-one backbone substituted with a dichlorophenyl group at one end and a dimethylphenyl group at the other. The presence of the dichlorophenyl moiety indicates potential for significant biological activity, as halogenated aromatic compounds often exhibit unique chemical properties and reactivity. The dimethylphenyl group contributes to the compound's hydrophobic characteristics, influencing its solubility and interaction with biological systems. This compound may be of interest in various fields, including medicinal chemistry and materials science, due to its structural complexity and potential applications. Its synthesis and handling require standard laboratory safety protocols, as with many organic compounds, to mitigate risks associated with chemical exposure. Overall, the unique combination of substituents in this compound suggests potential for diverse applications in research and industry.

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

898793-29-8: 1-(3,4-Dichlorophenyl)-3-(2,3-dimethylphenyl)propan-1-one, with the CAS number 898793-29-8, is an organic compound characterized by its ketone functional group, specifically a propanone structure. This compound features a propan-1-one backbone substituted with a dichlorophenyl group at one end and a dimethylphenyl group at the other. The presence of the dichlorophenyl moiety indicates potential for significant biological activity, as halogenated aromatic compounds often exhibit unique chemical properties and reactivity. The dimethylphenyl group contributes to the compound's hydrophobic characteristics, influencing its solubility and interaction with biological systems. This compound may be of interest in various fields, including medicinal chemistry and materials science, due to its structural complexity and potential applications. Its synthesis and handling require standard laboratory safety protocols, as with many organic compounds, to mitigate risks associated with chemical exposure. Overall, the unique combination of substituents in this compound suggests potential for diverse applications in research and industry.

CAS 898793-29-8

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

3′,4′-dichloro-3-(2,3-dimethylphenyl)propiophenone

Ref: 10-F206401