New research progress on 5089-22-5 in 2021. Synthetic Route of 5089-22-5, Reactions catalyzed within inorganic and organic materials and at electrochemical interfaces commonly occur at high coverage and in condensed media, causing turnover rates to depend strongly on interfacial structure and composition, 5089-22-5, Name is 1,4-Bis(benzo[d]oxazol-2-yl)naphthalene, SMILES is C1(C2=NC3=CC=CC=C3O2)=C4C=CC=CC4=C(C5=NC6=CC=CC=C6O5)C=C1, belongs to naphthyridine compound. In a article, author is Fun, Hoong-Kun, introduce new discover of the category.
The asymmetric unit of the title compound, C10H10N2, contains one half-molecule with the two shared C atoms lying on a twofold rotation axis. The 1,8-naphthyridine is almost planar with a dihedral angle of 0.42 (3)degrees between the fused pyridine rings. In the crystal, molecules are linked into infinite chains along the c axis by intermolecular C-H center dot center dot center dot N hydrogen bonds, generating R-2(2)(8) ring motifs. In addition, the crystal structure is further stabilized by C-H center dot center dot center dot pi interactions.
Synthetic Route of 5089-22-5, 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 5089-22-5 is helpful to your research.
Reference:
1,8-Naphthyridine – Wikipedia,
,1,8-Naphthyridine | C8H6N2 – PubChem