Recommanded Product: Dimethyl 2-(4-nitrophenyl)malonateOn May 18, 1998 ,《Solvent effects for proton transfer reaction from dimethyl (4-nitrophenyl)malonate to cis-1,2-bis(diethylaminomethyl)cyclohexane》 appeared in Journal of Molecular Structure. The author of the article were Schroeder, Grzegorz; Leska, Boguslawa; Brzezinski, Boguml. The article conveys some information:
The influence of polar aprotic solvents: DMSO, AN and HMPA on the kinetics of proton transfer reactions from dimethyl(4-nitrophenyl)malonate (C-acid) to cis-1,2-bis-(diethylaminomethyl)cyclohexane (DEAMCH) was studied. On the basis of the kinetic parameters obtained, the multistep mechanism of deprotonation processes and the influence of solvation on transition state were discussed. In the experiment, the researchers used Dimethyl 2-(4-nitrophenyl)malonate(cas: 4033-88-9Recommanded Product: Dimethyl 2-(4-nitrophenyl)malonate)
Dimethyl 2-(4-nitrophenyl)malonate(cas: 4033-88-9) belongs to esters. Esters are more polar than ethers but less polar than alcohols. They participate in hydrogen bonds as hydrogen-bond acceptors, but cannot act as hydrogen-bond donors, unlike their parent alcohols. Recommanded Product: Dimethyl 2-(4-nitrophenyl)malonate
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics