CAS 141236-46-6

2-Propenoyl chloride, 3-(3,4-dimethoxyphenyl)-, (E)-

Description:

2-Propenoyl chloride, 3-(3,4-dimethoxyphenyl)-, (E)- is an organic compound characterized by its functional groups and structural features. It contains an acyl chloride group, which makes it reactive and useful in various chemical reactions, particularly in acylation processes. The presence of the 3-(3,4-dimethoxyphenyl) substituent indicates that it has a phenyl ring with two methoxy groups, contributing to its aromatic character and potentially influencing its reactivity and solubility. The (E)- configuration denotes that the substituents on the double bond are on opposite sides, which can affect the compound's physical properties and reactivity. This compound is likely to be a colorless to pale yellow liquid, exhibiting a pungent odor typical of acyl chlorides. It is important to handle this substance with care due to its reactivity, particularly with water and alcohols, which can lead to hydrolysis and the formation of corresponding acids. Overall, its unique structure makes it a valuable intermediate in organic synthesis and pharmaceutical applications.

Formula: C₁₁H₁₁ClO₃

3-(3,4-Dimethoxyphenyl)prop-2-enoyl chloride

CAS: 141236-46-6

3-(3,4-Dimethoxyphenyl)prop-2-enoyl chloride is a lactone that can be used for coupling reactions. It is a triester of quinic acid and 3,4-dimethoxybenzene propionic acid. 3-(3,4-Dimethoxyphenyl)prop-2-enoyl chloride is prepared by the reaction of 3,4-dimethoxyphenol with chloroacetic acid and sodium ethoxide in ethanol. This product has been shown to inhibit the growth of bacteria by inhibiting protein synthesis and cell division.

Formula: C₁₁H₁₁ClO₃

Purity: Min. 95%

Molecular weight: 226.65 g/mol

Ref: 3D-RFA23646