Name: Dimethyl 2-(4-nitrophenyl)malonateOn October 31, 1996 ,《Proton transfer reactions from dimethyl (4-nitrophenyl)malonate to N-bases in acetonitrile》 was published in Journal of Molecular Structure. The article was written by Schroeder, Grzegorz; Brzezinski, Bogumil; Jarczewski, Arnold; Grech, Eugeniusz; Milart, Piotr. The article contains the following contents:
Deprotonations of di-Me (4-nitrophenyl)malonate (C-acid) by 7-methyl-1,5,7-triazabicyclo[4.4.0]dec-5-ene (MTBD), 1,5,7-triazabicyclo[4.4.0]dec-5-ene (TBD) and 1,8-bis(dimethylamino)naphthalene (DMAN) in acetonitrile were studied by kinetic as well as FTIR and 1H NMR spectroscopic methods. In the 1:1 mixture of C-acid with DMAN no proton transfer was found. The N-bases with guanidine-like character deprotonate C-acid in the acetonitrile solution quant. The mechanisms of proton transfer reactions are discussed.Dimethyl 2-(4-nitrophenyl)malonate(cas: 4033-88-9Name: Dimethyl 2-(4-nitrophenyl)malonate) was used in this study.
Dimethyl 2-(4-nitrophenyl)malonate(cas: 4033-88-9) belongs to esters. They are important in biology, being one of the main classes of lipids and comprising the bulk of animal fats and vegetable oils.Name: Dimethyl 2-(4-nitrophenyl)malonate They perform as high-grade solvents for a broad array of plastics, plasticizers, resins, and lacquers, and are one of the largest classes of synthetic lubricants on the commercial market. Polyesters are important plastics, with monomers linked by ester moieties.
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics