1-(2,5-Dichlorophenyl)-3-(4-methoxyphenyl)propan-1-one, identified by its CAS number 898776-28-8, is an organic compound characterized by its complex structure featuring a propanone backbone substituted with both a dichlorophenyl group and a methoxyphenyl group. This compound typically exhibits properties associated with ketones, such as being a colorless to pale yellow solid or liquid, depending on its purity and specific conditions. It is likely to be soluble in organic solvents like ethanol and dichloromethane, while being less soluble in water due to its hydrophobic aromatic groups. The presence of chlorine atoms in the dichlorophenyl moiety may impart unique electronic properties, potentially influencing its reactivity and interactions in chemical reactions. Additionally, the methoxy group can enhance the compound's lipophilicity and may affect its biological activity. This compound may be of interest in pharmaceutical research or as an intermediate in organic synthesis, although specific applications would depend on further studies of its properties and behavior in various chemical contexts.

1-(2,5-dichlorophenyl)-3-(4-methoxyphenyl)propan-1-one

898776-28-8: 1-(2,5-Dichlorophenyl)-3-(4-methoxyphenyl)propan-1-one, identified by its CAS number 898776-28-8, is an organic compound characterized by its complex structure featuring a propanone backbone substituted with both a dichlorophenyl group and a methoxyphenyl group. This compound typically exhibits properties associated with ketones, such as being a colorless to pale yellow solid or liquid, depending on its purity and specific conditions. It is likely to be soluble in organic solvents like ethanol and dichloromethane, while being less soluble in water due to its hydrophobic aromatic groups. The presence of chlorine atoms in the dichlorophenyl moiety may impart unique electronic properties, potentially influencing its reactivity and interactions in chemical reactions. Additionally, the methoxy group can enhance the compound's lipophilicity and may affect its biological activity. This compound may be of interest in pharmaceutical research or as an intermediate in organic synthesis, although specific applications would depend on further studies of its properties and behavior in various chemical contexts.

CAS 898776-28-8

1-(2,5-dichlorophenyl)-3-(4-methoxyphenyl)propan-1-one

2′,5′-dichloro-3-(4-methoxyphenyl)propiophenone

Ref: 10-F205923