Synthetic Route of C7H8BrNO. 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: 2-Bromo-1-(1-methyl-1H-pyrrol-2-yl)ethanone, is researched, Molecular C7H8BrNO, CAS is 65438-97-3, about Pyrrole analogues of chloramphenicol. I. Synthesis and antibacterial activity of dl-threo-1-(1-methyl-4-nitro-pyrrole-2-yl)-2-dichloroacetamidopropane-1,3-diol. Author is Krajewska, Dorota; Dabrowska, Marta; Jakoniuk, Piotr; Rozanski, Andrzej.
The seven step synthesis of the title pyrrole analog (I) of chloramphenicol was described. The compound exhibits a significant antibacterial activity, over the 12-50% range of the chloramphenicol activity.
After consulting a lot of data, we found that this compound(65438-97-3)Synthetic Route of C7H8BrNO can be used in many types of reactions. And in most cases, this compound has more advantages.
Reference:
1,8-Naphthyridine – Wikipedia,
1,8-Naphthyridine | C8H6N2 – PubChem