1-(3,4-Dichlorophenyl)-3-(m-tolyl)propan-1-one, identified by its CAS number 898768-10-0, is an organic compound characterized by its ketone functional group. This substance features a propanone backbone with a dichlorophenyl group and a m-tolyl group attached, contributing to its unique chemical properties. The presence of the dichlorophenyl moiety suggests that it may exhibit significant biological activity, potentially influencing its reactivity and interactions in various chemical environments. The compound is likely to be a solid at room temperature, given its structure, and may have moderate solubility in organic solvents. Its molecular structure indicates potential applications in pharmaceuticals or as an intermediate in organic synthesis. Additionally, the presence of chlorine atoms can enhance its lipophilicity, affecting its behavior in biological systems. Safety and handling precautions should be observed due to the potential toxicity associated with chlorinated compounds. Overall, this compound exemplifies the complexity and diversity of organic chemistry, particularly in the realm of substituted aromatic ketones.

1-(3,4-dichlorophenyl)-3-(m-tolyl)propan-1-one

898768-10-0: 1-(3,4-Dichlorophenyl)-3-(m-tolyl)propan-1-one, identified by its CAS number 898768-10-0, is an organic compound characterized by its ketone functional group. This substance features a propanone backbone with a dichlorophenyl group and a m-tolyl group attached, contributing to its unique chemical properties. The presence of the dichlorophenyl moiety suggests that it may exhibit significant biological activity, potentially influencing its reactivity and interactions in various chemical environments. The compound is likely to be a solid at room temperature, given its structure, and may have moderate solubility in organic solvents. Its molecular structure indicates potential applications in pharmaceuticals or as an intermediate in organic synthesis. Additionally, the presence of chlorine atoms can enhance its lipophilicity, affecting its behavior in biological systems. Safety and handling precautions should be observed due to the potential toxicity associated with chlorinated compounds. Overall, this compound exemplifies the complexity and diversity of organic chemistry, particularly in the realm of substituted aromatic ketones.

CAS 898768-10-0

1-(3,4-dichlorophenyl)-3-(m-tolyl)propan-1-one

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

Ref: 10-F205712