Ethyl 2-(4-methoxyphenyl)-2-methylpropanoate, with the CAS number 2901-19-1, is an organic compound belonging to the class of esters. It features a branched alkyl chain and an aromatic ring, which contributes to its unique chemical properties. The presence of the methoxy group (-OCH3) on the phenyl ring enhances its electron-donating characteristics, potentially influencing its reactivity and solubility in organic solvents. This compound is typically a colorless to pale yellow liquid with a pleasant odor, making it useful in flavor and fragrance applications. Its molecular structure suggests it may exhibit moderate volatility and a relatively low boiling point, common for esters. Ethyl 2-(4-methoxyphenyl)-2-methylpropanoate is likely to be soluble in organic solvents like ethanol and ether but less soluble in water due to its hydrophobic characteristics. Additionally, it may participate in various chemical reactions typical of esters, such as hydrolysis and transesterification, making it a versatile compound in synthetic organic chemistry.

ethyl 2-(4-methoxyphenyl)-2-methylpropanoate

2901-19-1: Ethyl 2-(4-methoxyphenyl)-2-methylpropanoate, with the CAS number 2901-19-1, is an organic compound belonging to the class of esters. It features a branched alkyl chain and an aromatic ring, which contributes to its unique chemical properties. The presence of the methoxy group (-OCH3) on the phenyl ring enhances its electron-donating characteristics, potentially influencing its reactivity and solubility in organic solvents. This compound is typically a colorless to pale yellow liquid with a pleasant odor, making it useful in flavor and fragrance applications. Its molecular structure suggests it may exhibit moderate volatility and a relatively low boiling point, common for esters. Ethyl 2-(4-methoxyphenyl)-2-methylpropanoate is likely to be soluble in organic solvents like ethanol and ether but less soluble in water due to its hydrophobic characteristics. Additionally, it may participate in various chemical reactions typical of esters, such as hydrolysis and transesterification, making it a versatile compound in synthetic organic chemistry.

CAS 2901-19-1

ethyl 2-(4-methoxyphenyl)-2-methylpropanoate

ethyl 2-(4-methoxyphenyl)-2-methylpropanoate

Ref: IN-DA002V7H

Ethyl 2-(4-methoxyphenyl)-2-methylpropanoate

Ref: 3D-CAA90119