The preparation of ester heterocycles mostly uses heteroatoms as nucleophilic sites, which are achieved by intramolecular substitution or addition reactions. Compound: 3-Bromo-4-chloronitrobenzene( cas:16588-26-4 ) is researched.Recommanded Product: 16588-26-4.Liedholm, Brita published the article 《Copper(I)-induced bromine-hydrogen exchange of 2,3-dibromoanilines》 about this compound( cas:16588-26-4 ) in Acta Chemica Scandinavica, Series B: Organic Chemistry and Biochemistry. Keywords: copper reduction dibromoaniline; aniline dibromo debromination copper; debromination dibromoaniline copper ion. Let’s learn more about this compound (cas:16588-26-4).
The Cu(I)-induced Br/H exchange reaction of 2,3-dibromoaniline and 5-substituted 2,3-dibromoanilines in the 2-position has been kinetically studied in aqueous HOAc-HCl medium at 90°. The dehalogenation reaction is 2nd order, 1st in both substrate and Cu+, and may be interpreted as a reductive substitution, composed of two 1-electron steps. The 2,3-dibromophenol was only qual. examined but gave similar results.
There is still a lot of research devoted to this compound(SMILES：BrC1=C(C=CC(=C1)[N+](=O)[O-])Cl)Recommanded Product: 16588-26-4, and with the development of science, more effects of this compound(16588-26-4) can be discovered.
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