Discovery of 88847-89-6

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions. you can also check out more blogs about 88847-89-6. Category: naphthyridines.

Chemistry, like all the natural sciences, begins with the direct observation of nature— in this case, of matter.88847-89-6, Name is 2-Amino-9-((2R,4S,5R)-4-hydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-3H-purine-6,8(7H,9H)-dione, SMILES is O=C1N=C(N)NC2=C1NC(N2[C@@H]3O[C@H](CO)[C@@H](O)C3)=O, belongs to naphthyridine compound. In a document, author is Tarasov, Andrii V., introduce the new discover, Category: naphthyridines.

14-(2,3-Dichlorophenyl)-9,10-dimethylbenzimidazo[1,2-a]benzo[f][1,8]naphthyridine-6-carbonitrile

In the title compound, C27H16Cl2N4, the benzimidazo[1,2-a]benzo[f][1,8]naphthyridine system is nearly planar (r.m.s. deviation for all non-H atoms = 0.033 angstrom). The dichlorophenyl substituent is rotated by -67.5 (2)degrees from this plane. In the crystal structure, molecules form stacks along the crystallographic (100) direction due to pi-pi stacking interactions with a centroid-centroid distance of 3.4283 (9) angstrom.

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions. you can also check out more blogs about 88847-89-6. Category: naphthyridines.

Reference:
1,8-Naphthyridine – Wikipedia,
,1,8-Naphthyridine | C8H6N2 – PubChem