Ethyl 3-(2,6-dimethoxyphenyl)-3-oxopropanoate, with the CAS number 125732-13-0, is an organic compound characterized by its ester functional group and a ketone moiety. This compound features a propanoate backbone, where the ethyl group is attached to the ester, contributing to its solubility in organic solvents. The presence of the 2,6-dimethoxyphenyl substituent enhances its aromatic properties and may influence its reactivity and interaction with biological systems. Typically, compounds of this nature exhibit moderate to high lipophilicity due to the aromatic ring and alkyl groups, which can affect their pharmacokinetic profiles if considered for pharmaceutical applications. Additionally, the methoxy groups can provide electron-donating effects, potentially influencing the compound's reactivity in electrophilic aromatic substitution reactions. Overall, this compound's unique structure suggests potential utility in organic synthesis and medicinal chemistry, although specific applications would depend on further research into its biological activity and chemical behavior.

ETHYL 3-(2,6-DIMETHOXYPHENYL)-3-OXOPROPANOATE

125732-13-0: Ethyl 3-(2,6-dimethoxyphenyl)-3-oxopropanoate, with the CAS number 125732-13-0, is an organic compound characterized by its ester functional group and a ketone moiety. This compound features a propanoate backbone, where the ethyl group is attached to the ester, contributing to its solubility in organic solvents. The presence of the 2,6-dimethoxyphenyl substituent enhances its aromatic properties and may influence its reactivity and interaction with biological systems. Typically, compounds of this nature exhibit moderate to high lipophilicity due to the aromatic ring and alkyl groups, which can affect their pharmacokinetic profiles if considered for pharmaceutical applications. Additionally, the methoxy groups can provide electron-donating effects, potentially influencing the compound's reactivity in electrophilic aromatic substitution reactions. Overall, this compound's unique structure suggests potential utility in organic synthesis and medicinal chemistry, although specific applications would depend on further research into its biological activity and chemical behavior.

CAS 125732-13-0

ETHYL 3-(2,6-DIMETHOXYPHENYL)-3-OXOPROPANOATE

Benzenepropanoic acid, 2,6-dimethoxy-β-oxo-, ethyl ester

Ref: IN-DA000OL5

Ethyl 3-(2,6-dimethoxyphenyl)-3-oxopropanoate

Ref: 54-OR1058904

ethyl 3-(2,6-dimethoxyphenyl)-3-oxopropanoate

Ref: 10-F522342