The chemical substance known as [3-(Acetyloxy)phenyl](2,4-dimethylphenyl)methanone, with the CAS number 890099-08-8, is an organic compound characterized by its complex structure, which includes a phenyl ring substituted with an acetyloxy group and a methanone moiety. This compound typically exhibits properties associated with ketones and esters, such as moderate polarity and potential reactivity due to the presence of the carbonyl group. Its molecular structure suggests that it may participate in various chemical reactions, including nucleophilic substitutions and electrophilic aromatic substitutions. The acetyloxy group can influence the compound's solubility and reactivity, making it potentially useful in synthetic organic chemistry. Additionally, the presence of multiple methyl groups on the phenyl ring may enhance its hydrophobic characteristics. Overall, this compound's unique functional groups and structural features may contribute to its applications in pharmaceuticals, agrochemicals, or as intermediates in organic synthesis. However, specific properties such as melting point, boiling point, and solubility would require empirical data for precise characterization.

[3-(Acetyloxy)phenyl](2,4-dimethylphenyl)methanone

890099-08-8: The chemical substance known as [3-(Acetyloxy)phenyl](2,4-dimethylphenyl)methanone, with the CAS number 890099-08-8, is an organic compound characterized by its complex structure, which includes a phenyl ring substituted with an acetyloxy group and a methanone moiety. This compound typically exhibits properties associated with ketones and esters, such as moderate polarity and potential reactivity due to the presence of the carbonyl group. Its molecular structure suggests that it may participate in various chemical reactions, including nucleophilic substitutions and electrophilic aromatic substitutions. The acetyloxy group can influence the compound's solubility and reactivity, making it potentially useful in synthetic organic chemistry. Additionally, the presence of multiple methyl groups on the phenyl ring may enhance its hydrophobic characteristics. Overall, this compound's unique functional groups and structural features may contribute to its applications in pharmaceuticals, agrochemicals, or as intermediates in organic synthesis. However, specific properties such as melting point, boiling point, and solubility would require empirical data for precise characterization.

CAS 890099-08-8

[3-(Acetyloxy)phenyl](2,4-dimethylphenyl)methanone

3-Acetoxy-2',4'-dimethylbenzophenone

Ref: IN-DA0044R9

3-Acetoxy-2′,4′-dimethylbenzophenone

Ref: 10-F201825