(3,5-Dimethoxyphenyl)acetone, with the CAS number 18917-77-6, is an organic compound characterized by its aromatic structure and functional groups. It features a phenyl ring substituted with two methoxy groups at the 3 and 5 positions, which enhances its electron-donating properties and affects its reactivity and solubility. The acetone moiety contributes to its ketone functionality, making it a potential candidate for various chemical reactions, including condensation and oxidation. This compound is typically a colorless to pale yellow liquid or solid, depending on its purity and form. Its molecular structure suggests it may exhibit interesting biological activities, making it of interest in pharmaceutical and chemical research. Additionally, the presence of methoxy groups can influence its interaction with biological systems, potentially affecting its pharmacokinetics and pharmacodynamics. As with many organic compounds, safety precautions should be taken when handling (3,5-dimethoxyphenyl)acetone, as it may pose health risks if ingested or inhaled.

(3,5-DIMETHOXYPHENYL)ACETONE

18917-77-6: (3,5-Dimethoxyphenyl)acetone, with the CAS number 18917-77-6, is an organic compound characterized by its aromatic structure and functional groups. It features a phenyl ring substituted with two methoxy groups at the 3 and 5 positions, which enhances its electron-donating properties and affects its reactivity and solubility. The acetone moiety contributes to its ketone functionality, making it a potential candidate for various chemical reactions, including condensation and oxidation. This compound is typically a colorless to pale yellow liquid or solid, depending on its purity and form. Its molecular structure suggests it may exhibit interesting biological activities, making it of interest in pharmaceutical and chemical research. Additionally, the presence of methoxy groups can influence its interaction with biological systems, potentially affecting its pharmacokinetics and pharmacodynamics. As with many organic compounds, safety precautions should be taken when handling (3,5-dimethoxyphenyl)acetone, as it may pose health risks if ingested or inhaled.

1-(3,5-dimethoxyphenyl)propan-2-one

<p>(3,5-Dimethoxyphenyl)acetone is a plant phenolic compound that has been found in many plants. It is an intermediate in the biosynthesis of lignans and a wide range of other natural products. The production of (3,5-dimethoxyphenyl)acetone by plants is induced by the presence of nitrate, chloride and/or tyrosol. This compound also represses the expression of genes involved in dextrose metabolism and carbon fixation pathways. Furthermore, it can be quantified using isotopic labelling techniques and has been detected at low levels in human urine samples.</p>

CAS 18917-77-6

(3,5-DIMETHOXYPHENYL)ACETONE

1-(3,5-dimethoxyphenyl)propan-2-one

Ref: IN-DA002HZS

(3,5-Dimethoxyphenyl)acetone

Ref: 3D-FD67878