[3-(2,5-Dimethoxybenzoyl)phenyl] acetate, with the CAS number 890100-38-6, is an organic compound characterized by its complex structure, which includes a phenyl ring substituted with an acetate group and a benzoyl moiety featuring two methoxy groups. This compound typically exhibits properties associated with aromatic compounds, such as stability and potential for various chemical reactions, including electrophilic substitutions. The presence of methoxy groups enhances its solubility in organic solvents and may influence its reactivity and interaction with biological systems. Additionally, the acetyl group contributes to its overall polarity, affecting its physical properties like melting and boiling points. The compound may also exhibit interesting biological activities, making it a subject of interest in medicinal chemistry. Its synthesis often involves acylation reactions, and it can be analyzed using techniques such as NMR spectroscopy and mass spectrometry to confirm its structure and purity. Overall, [3-(2,5-dimethoxybenzoyl)phenyl] acetate is a versatile compound with potential applications in various fields, including pharmaceuticals and materials science.

[3-(2,5-dimethoxybenzoyl)phenyl] acetate

890100-38-6: [3-(2,5-Dimethoxybenzoyl)phenyl] acetate, with the CAS number 890100-38-6, is an organic compound characterized by its complex structure, which includes a phenyl ring substituted with an acetate group and a benzoyl moiety featuring two methoxy groups. This compound typically exhibits properties associated with aromatic compounds, such as stability and potential for various chemical reactions, including electrophilic substitutions. The presence of methoxy groups enhances its solubility in organic solvents and may influence its reactivity and interaction with biological systems. Additionally, the acetyl group contributes to its overall polarity, affecting its physical properties like melting and boiling points. The compound may also exhibit interesting biological activities, making it a subject of interest in medicinal chemistry. Its synthesis often involves acylation reactions, and it can be analyzed using techniques such as NMR spectroscopy and mass spectrometry to confirm its structure and purity. Overall, [3-(2,5-dimethoxybenzoyl)phenyl] acetate is a versatile compound with potential applications in various fields, including pharmaceuticals and materials science.

CAS 890100-38-6

[3-(2,5-dimethoxybenzoyl)phenyl] acetate

3-Acetoxy-2',5'-dimethoxybenzophenone

Ref: IN-DA0044NO

3-Acetoxy-2′,5′-dimethoxybenzophenone

Ref: 10-F201820