New Advances in Chemical Research, April 2021. Application of 1588-83-6, The appropriate choice of redox mediator can avoid electrode passivation and overpotential, which strongly inhibit the efficient activation of substrates in electrolysis. 1588-83-6, Name is 4-Amino-3-nitrobenzoic acid, SMILES is C1=C([N+]([O-])=O)C(=CC=C1C(=O)O)N, belongs to naphthyridine compound. In a article, author is Hossaini, Zinatossadat, introduce new discover of the category.
The Fe3O4/ZnO/MWCNTs magnetic nanocomposites as a high performance organomettalic catalyst was employed for the preparation of naphthyridine derivatives in high yields via five component reaction of isoquinoline, dialkyl acetylenedicarboxylates or propiolates, alpha-haloketones, triphenyphophine and ammonium acetate in aqueous media at ambient temperature. The Fe3O4/ZnO/MWCNTs MNCs were synthesized using ionic liquid [OMIM]Br as a stabilizer and soft template. As well Fe3O4/ZnO/MWCNTs MNCs show a good improvement in the yield of the product and showed significant reusable ability. Due to having isoquinoline core, we investigate antioxidant property of some synthesized compounds by diphenyl-picrylhydrazine (DPPH) radical trapping and power of ferric reduction experiment. Furthermore, the disk diffusion test on Gram positive and negative bacteria are utilized for investigation of antimicrobial activity of some naphthyridines. The achieved outcomes of this experiment demonstrate that these synthesized compounds could prevent from growth of bacteria. Short time of reaction, high yields of product, easy separation of catalyst and products are some benefits of this process.
Application of 1588-83-6, Enzymes are biological catalysts that produce large increases in reaction rates and tend to be specific for certain reactants and products. I hope my blog about 1588-83-6 is helpful to your research.
Reference:
1,8-Naphthyridine – Wikipedia,
,1,8-Naphthyridine | C8H6N2 – PubChem