New Advances in Chemical Research, April 2021. Application of 13331-27-6, The appropriate choice of redox mediator can avoid electrode passivation and overpotential, which strongly inhibit the efficient activation of substrates in electrolysis. 13331-27-6, Name is 3-Nitrophenylboronic acid, SMILES is C1=C(C=CC=C1[N+]([O-])=O)B(O)O, belongs to naphthyridine compound. In a article, author is Mogilaiah, K., introduce new discover of the category.
A simple, rapid and efficient protocol for the synthesis of beta-enaminones (5,5-dimethyl-3-) [(3-aryl [1,8) naphthyridine-2-yl] amino]-2-cyclohexene-1-ones) 3 has been achieved by the reaction of 2-amino-3-aryl-1,8-naphthyridines 1 with dimedone (5,5-dimethyl-cyclohexa-1,3-dione) 2 in the presence of montmorillonite K10 clay under solvent-free conditions using microwave irradiation. The products are obtained in very good yields and in a state of high purity.
Application of 13331-27-6, Consequently, the presence of a catalyst will permit a system to reach equilibrium more quickly, but it has no effect on the position of the equilibrium as reflected in the value of its equilibrium constant.I hope my blog about 13331-27-6 is helpful to your research.
Reference:
1,8-Naphthyridine – Wikipedia,
,1,8-Naphthyridine | C8H6N2 – PubChem