Introduction of a new synthetic route about 87488-84-4

This compound(1-(2-Bromophenyl)-1H-pyrazole)Electric Literature of C9H7BrN2 was discussed at the molecular level, the effects of temperature and reaction time on the properties of the compound were discussed, and the optimum reaction conditions were selected.

Heterocyclic compounds can be divided into two categories: alicyclic heterocycles and aromatic heterocycles. Compounds whose heterocycles in the molecular skeleton cannot reflect aromaticity are called alicyclic heterocyclic compounds. Compound: 87488-84-4, is researched, Molecular C9H7BrN2, about Chemoselective and regiospecific formylation of 1-phenyl-1H-pyrazoles through the Duff reaction, the main research direction is phenylpyrazoles with hexamethylenetetramine Duff formylation.Electric Literature of C9H7BrN2.

The synthesis of formylated 1-phenyl-1H-pyrazole derivatives under the Duff reaction conditions was reported. The results indicated that 1-phenyl-1H-pyrazole systems containing electron-withdrawing and donating substituents at the Ph moiety react under the Duff reaction conditions to furnish formylated derivatives in good yields.

This compound(1-(2-Bromophenyl)-1H-pyrazole)Electric Literature of C9H7BrN2 was discussed at the molecular level, the effects of temperature and reaction time on the properties of the compound were discussed, and the optimum reaction conditions were selected.

Reference:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem