3-(2,4-Dimethylphenyl)-1-[3-(trifluoromethyl)phenyl]propan-1-one, with the CAS number 898794-32-6, is an organic compound characterized by its complex structure featuring a propanone backbone substituted with two distinct aromatic groups. The presence of a 2,4-dimethylphenyl group contributes to its hydrophobic nature, while the trifluoromethyl group enhances its electronic properties, making it potentially useful in various chemical applications. This compound is likely to exhibit significant lipophilicity due to the bulky aromatic substituents, which may influence its solubility in organic solvents. Additionally, the trifluoromethyl group can impart unique reactivity and stability characteristics, often making such compounds of interest in medicinal chemistry and material science. The compound's synthesis and reactivity can be influenced by the steric and electronic effects of its substituents, which may also affect its biological activity. Overall, this compound represents a class of substituted ketones that may have applications in pharmaceuticals or as intermediates in organic synthesis.

3-(2,4-dimethylphenyl)-1-[3-(trifluoromethyl)phenyl]propan-1-one

898794-32-6: 3-(2,4-Dimethylphenyl)-1-[3-(trifluoromethyl)phenyl]propan-1-one, with the CAS number 898794-32-6, is an organic compound characterized by its complex structure featuring a propanone backbone substituted with two distinct aromatic groups. The presence of a 2,4-dimethylphenyl group contributes to its hydrophobic nature, while the trifluoromethyl group enhances its electronic properties, making it potentially useful in various chemical applications. This compound is likely to exhibit significant lipophilicity due to the bulky aromatic substituents, which may influence its solubility in organic solvents. Additionally, the trifluoromethyl group can impart unique reactivity and stability characteristics, often making such compounds of interest in medicinal chemistry and material science. The compound's synthesis and reactivity can be influenced by the steric and electronic effects of its substituents, which may also affect its biological activity. Overall, this compound represents a class of substituted ketones that may have applications in pharmaceuticals or as intermediates in organic synthesis.

CAS 898794-32-6

3-(2,4-dimethylphenyl)-1-[3-(trifluoromethyl)phenyl]propan-1-one

3-(2,4-dimethylphenyl)-3′-trifluoromethylpropiophenone

Ref: 10-F206445