CAS 19037-58-2
:(3,5-DIMETHOXY-4-HYDROXYPHENYL)ACETONE
Description:
(3,5-Dimethoxy-4-hydroxyphenyl)acetone, with the CAS number 19037-58-2, is an organic compound characterized by its phenolic structure, which includes two methoxy groups and a hydroxyl group attached to a phenyl ring. This compound features an acetone moiety, contributing to its ketone functionality. The presence of the methoxy groups enhances its lipophilicity and may influence its biological activity, making it of interest in various fields, including medicinal chemistry and pharmacology. The hydroxyl group can participate in hydrogen bonding, potentially affecting its solubility and reactivity. Typically, compounds like this may exhibit antioxidant properties and could be investigated for their potential therapeutic effects. Its synthesis often involves the modification of phenolic compounds, and it may be analyzed using techniques such as NMR spectroscopy and mass spectrometry to confirm its structure and purity. Overall, (3,5-Dimethoxy-4-hydroxyphenyl)acetone represents a class of compounds that may have significant implications in chemical research and applications.
Formula:C11H14O4
InChI:InChI=1/C11H14O4/c1-7(12)4-8-5-9(14-2)11(13)10(6-8)15-3/h5-6,13H,4H2,1-3H3
SMILES:CC(=O)Cc1cc(c(c(c1)OC)O)OC
Synonyms:- 2-Propanone, 1-(4-hydroxy-3,5-dimethoxyphenyl)-
- 1-(4-Hydroxy-3,5-Dimethoxyphenyl)Propan-2-One
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Found 6 products.
2-Propanone, 1-(4-hydroxy-3,5-dimethoxyphenyl)-
CAS:Formula:C11H14O4Purity:95%Color and Shape:SolidMolecular weight:210.22651-(4-Hydroxy-3,5-dimethoxyphenyl)propan-2-one
CAS:1-(4-Hydroxy-3,5-dimethoxyphenyl)propan-2-onePurity:95%Molecular weight:210.23g/mol1-(4-Hydroxy-3,5-dimethoxyphenyl)propan-2-one
CAS:Formula:C11H14O4Purity:95%Color and Shape:SolidMolecular weight:210.229Syringylacetone-D₆
CAS:Controlled ProductFormula:C11H8D6O4Color and Shape:NeatMolecular weight:216.27(3,5-Dimethoxy-4-hydroxyphenyl)acetone
CAS:<p>(3,5-Dimethoxy-4-hydroxyphenyl)acetone is a phenolic compound that is used as a calibration standard in the analysis of tannins. It has been shown to have a catalytic effect on the oxidation of oleic acid and linoleic acid in the presence of peroxides. The addition of (3,5-dimethoxy-4-hydroxyphenyl)acetone to an oil or fat emulsion at room temperature leads to an increase in the viscosity of the emulsion. This compound can be found in many plants, such as tea and coffee beans, cocoa beans, and red wine grapes.</p>Formula:C11H14O4Purity:Min. 95%Color and Shape:Orange PowderMolecular weight:210.23 g/mol




