Academic researchers, R&D teams, teachers, students, policy makers and the media all rely on us to share knowledge that is reliable, accurate and cutting-edge. Related Products of 286961-14-6, The appropriate choice of redox mediator can avoid electrode passivation and overpotential, which strongly inhibit the efficient activation of substrates in electrolysis. 286961-14-6, Name is tert-Butyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-5,6-dihydropyridine-1(2H)-carboxylate, SMILES is O=C(N1CCC(B2OC(C)(C)C(C)(C)O2)=CC1)OC(C)(C)C, belongs to naphthyridine compound. In a article, author is Mo, Juan, introduce new discover of the category.
In the title salt, C(20)H(20)N(6)(2+)center dot 2ClO(4)(-), the cation is disposed about a center of symmetry at the mid-point of the N=N bond. The 1,8-naphthyridine systems are planar and the ten atoms have a mean deviation of 0.01 angstrom from the least-squares plane. The two planar 1,8-naphthyridine units are parallel but extend in opposite directions from the diazene bridge. The 1,8-naphthyridine aminium groups interact with perchlorate O atoms through N-H center dot center dot center dot O hydrogen bonds.
Related Products of 286961-14-6, Because enzymes can increase reaction rates by enormous factors and tend to be very specific, typically producing only a single product in quantitative yield, they are the focus of active research.you can also check out more blogs about 286961-14-6.
Reference:
1,8-Naphthyridine – Wikipedia,
,1,8-Naphthyridine | C8H6N2 – PubChem