Pyridine has a conjugated system of six π electrons that are delocalized over the ring. 1603-41-4, formula is C6H8N2, Name is 2-Amino-5-methylpyridine. The molecule is planar and, thus, follows the Hückel criteria for aromatic systems. COA of Formula: C6H8N2.
Kuthyala, Sharanya;Sheikh, Sareen;Nagaraja, G. K.;Kannika, B. R.;Madan Kumar, S.;Chandra Nayak, S.;Lokanath, N. K. research published 《 Towards the Synthesis of Imidazopyridine Derivatives: Characterization, Single Crystal XRD, Hirshfeld Analysis, and Biological Evaluation》, the research content is summarized as follows. This study explores the synthesis of different imidazopyridine derivatives, their characterization, single crystal x-ray diffraction, mol. Hirshfeld surface anal. along with their anticancer and other supportive biol. evaluations. X-ray crystallog. study resolved the crystal structure of 2,7-dimethyl-N-(1,3-dioxoisoindolin-2-yl)H-imidazo[1,2-a]pyridine-3-carboxamide as monoclinic crystal system (space group P21/n). Graphical tool, Hirshfeld surface anal. quantified the major contribution of H···H, O···H, and C···H interactions towards the HS. Among the synthesized compounds, 2-(4-(4-fluorophenyl)-5-(2,8-dimethyl-imidazo[1,2-a]pyridin-3-yl)-4H-1,2,4-triazol-3-ylthio)-N-(4-fluorophenyl)acetamide exhibited the highest cytotoxicity against lung adenocarcinoma with IC50 value of 43.04μM. Selective action of I was assured by cell death anal. using AO-EB assay. In addition, the study was also supported by mol. docking studies. Together the study revealed, the compound I to be a likely candidate for further exploratory study in cancer treatment.
1603-41-4, 2-Amino-5-methylpyridine, also known as 2-Amino-5-methylpyridine, is a useful research compound. Its molecular formula is C6H8N2 and its molecular weight is 108.14 g/mol. The purity is usually 95%.
2-Amino-5-methylpyridine is a chemical compound that belongs to the group of methyl ketones. It has a nitrogen atom and an oxygen atom in its structure, which allows it to form hydrogen bonds with other molecules. 2-Amino-5-methylpyridine can be obtained by reacting hydrochloric acid and xanthone in the presence of a base. The compound is highly reactive and has been shown to have antiinflammatory properties. This can be attributed to its ability to inhibit prostaglandin synthesis. 2-Amino-5-methylpyridine also has fluorescence properties that are sensitive to pH changes and can be used as a probe for metal ions. 2-Amino-5-methylpyridine is an organic compound that contains a methyl group, two nitrogen atoms, and one oxygen atom in its chemical structure. This molecule can form hydrogen bonds with other molecules due to its nitrogen atoms and oxygen atom,, COA of Formula: C6H8N2