Koller, Georg published the artcile< A synthesis of derivatives of 1,8-naphthyridine>, SDS of cas: 112-63-0, the main research area is .
K. learned of Seide’s work (C. A. 21, 586) only after the completion of his own investigation. Me α-aminonicotinate (1.5 g.) with Na in alc. and CH2(CO2Et)2 gives 1.26 g. Me 2,4-dihydroxy-1,8-naphthyridine-3-carboxylate, (the Et ester grouping in the CH2(CO2Et)2 being replaced by Me by the MeOH set free in the reaction), sinters in an evacuated tube on rapid heating at 236°, turns brown and carbonizes at higher temperatures, is strongly acid, dissolves in dilute Na2CO3, gives a distinct brown color with FeCl3 in alc.; heated a long time with dilute KOH it gives 2,4-dihydroxy-1,8-naphthyridine, sandy crystalline powder, gives a distinct yellow color with FeCl3 in alc., is strongly acid, dissolves clear in carbonates, slowly in dilute HCl, converted by POCl3 + PCl5 into the 2,4-dichloro compound, m. 125-6°; chloroaurate, yellow, sinters 200° (decomposition) in an evacuated tube, m. 210-2°.
Berichte der Deutschen Chemischen Gesellschaft [Abteilung] B: Abhandlungen published new progress about 112-63-0. 112-63-0 belongs to class esters-buliding-blocks, and the molecular formula is C19H34O2, SDS of cas: 112-63-0.
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics