Related Products of 6165-69-1, Redox catalysis has been broadly utilized in electrochemical synthesis due to its kinetic advantages over direct electrolysis. The appropriate choice of redox mediator can avoid electrode passivation and overpotential. 6165-69-1, Name is 3-Thiopheneboronic acid, SMILES is OB(C1=CSC=C1)O, belongs to naphthyridines compound. In a article, author is Vennila, K. N., introduce new discover of the category.
7-(2-Chlorophenyl)-2,6,9-trimethyldibenzo[b,h][1,6]naphthyridine
In the title compound, C(25)H(19)ClN(2), the dibenzo[b,h][1,6]-naphthyridine system is planar to within 0.16 (2) angstrom, and the chlorophenyl ring is inclined to it by 82.53 (7)degrees. In the crystal, molecules are linked by C-H center dot center dot center dot N hydrogen bonds, forming chains propagating in [100]. There are also a number of weak pi-pi stacking interactions present [centroid-centroid distances = 3.8531 (1) and 3.7631 (1) angstrom].
Related Products of 6165-69-1, Each elementary reaction can be described in terms of its molecularity, the number of molecules that collide in that step. The slowest step in a reaction mechanism is the rate-determining step.you can also check out more blogs about 6165-69-1.
Reference:
1,8-Naphthyridine – Wikipedia,
,1,8-Naphthyridine | C8H6N2 – PubChem