Application In Synthesis of Ethyl 3-Ethoxy-2-Propenoate. The protonation of heteroatoms in aromatic heterocycles can be divided into two categories: lone pairs of electrons are in the aromatic ring conjugated system; and lone pairs of electrons do not participate. Compound: Ethyl 3-Ethoxy-2-Propenoate, is researched, Molecular C7H12O3, CAS is 1001-26-9, about Schiff bases of mixed β-dicarbonyl compounds as tetradentate ligands in unsymmetrical chelate complexes. Author is Jaeger, Ernst G.; Seidel, Dietrich.
1,2-Benzenediamine was condensed with 1-methoxy-1-butene-3-one or Et 2-(ethoxymethylene)acetate (I) and then with I, 3-(ethoxymethylenepentane-2,4-dion, or di-Et ethoxymethylenemalonate to give CH3C(O)CR:CHNHC6H4(NHCH:CR1C(O)R2-2) (R = H, R1 = CH3, R2 = CO2Et; R = CO2Et, R1 = Me, R2 = COMe; R = CO2Et, R1 = OEt, R2 = CO2Et). The unsym. Schiff bases form Ni and Co complexes.
In some applications, this compound(1001-26-9)Application In Synthesis of Ethyl 3-Ethoxy-2-Propenoate is unique.If you want to know more details about this compound, you can contact with the author or consult more relevant literature.
Reference:
Bromide – Wikipedia,
bromide – Wiktionary