Ethyl (4-cyanophenyl)(oxo)acetate, identified by its CAS number 302912-31-8, is an organic compound characterized by its ester functional group and the presence of a cyano group attached to a phenyl ring. This compound typically exhibits a moderate to high polarity due to the presence of both the ester and cyano functionalities, which can influence its solubility in various solvents. Ethyl (4-cyanophenyl)(oxo)acetate may display interesting reactivity patterns, making it a potential candidate for use in organic synthesis, particularly in the development of pharmaceuticals or agrochemicals. Its structure suggests that it could participate in nucleophilic addition reactions, and the cyano group may also serve as a useful handle for further functionalization. Additionally, the compound's stability and reactivity can be affected by environmental factors such as temperature and pH. Overall, this compound's unique structural features contribute to its potential applications in various chemical processes.

ethyl (4-cyanophenyl)(oxo)acetate

302912-31-8: Benzeneacetic Acid, 4-Cyano-Alpha-Oxo-, Ethyl Ester, Ethyl-4-Cyanobenzoylformate

Ethyl 2-(4-cyanophenyl)-2-oxoacetate is a substrate for the Friedel-Crafts reaction. It is a synthetically derived compound that has been expressed in recombinant bacteria and can be used as a substrate for the kinetic resolution of racemic mixtures of chiral alcohols. The enantioselectivity of this substrate has been shown to be enhanced by dehydrogenase activity and kinetic parameters. Modifications to the substrate structure have also led to an increase in hydrogen bonding, which enhances the hexane solubility.

CAS 302912-31-8: ethyl (4-cyanophenyl)(oxo)acetate

Ethyl 2-(4-cyanophenyl)-2-oxoacetate

Ref: 3D-CMA91231

Ethyl 2-(4-cyanophenyl)-2-oxoacetate

Ref: 54-OR90404

Ethyl 4-cyanobenzoylformate

Ref: 10-F200950

Benzeneacetic acid, 4-cyano-α-oxo-, ethyl ester

Ref: IN-DA002ZI9