Archives for Chemistry Experiments of 3-Aminobenzofuran-2-carboxamide

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Synthetic Route of 54802-10-7, Because a catalyst decreases the height of the energy barrier, its presence increases the reaction rates of both the forward and the reverse reactions by the same amount.54802-10-7, Name is 3-Aminobenzofuran-2-carboxamide, molecular formula is C9H8N2O2. In a article,once mentioned of 54802-10-7

Titanium(III) chloride reacts with schiff bases derived from benzaldehydes/acetophenone with 3-amino-2-benzofuran carboxamide/ethyl-3-amino- 2-benzofuran carboxylate to yield complexes having general composition[Ti.2L. 2H2O]Cl3 (where L=schiff base). The ligands and their corresponding Ti(III) complexes have been characterised by elemental analyses, molar conductance,magnetic susceptibility, IR & electronic spectra and TGA. The ligands act in a bidentate manner. Based on these studies octahedral geometries have been proposed for these complexes. The ligands and their Ti(III)complexes have screened for antibacterial activities.

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Reference:
Benzofuran – Wikipedia,
Benzofuran | C8H2826O – PubChem