Roslan, Irwan Iskandar team published research in Asian Journal of Organic Chemistry in 2021 | 1603-41-4

Product Details of C6H8N2, 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,, 1603-41-4.

Pyridine is diamagnetic and has a diamagnetic susceptibility of −48.7 × 10−6 cm3·mol−1.The molecular electric dipole moment is 2.2 debyes. 1603-41-4, formula is C6H8N2, Name is 2-Amino-5-methylpyridine. TThe standard enthalpy of formation is 100.2 kJ·mol−1 in the liquid phase and 140.4 kJ·mol−1 in the gas phase. Product Details of C6H8N2.

Roslan, Irwan Iskandar;Ng, Kian-Hong;Alhooshani, Khalid R.;Jaenicke, Stephan;Chuah, Gaik-Khuan research published 《 In/Cu Catalyzed Multiple C-N/C-C Bond Formation via Multiple Bond Cleavage in a Three Component Synthesis of Arylimidazopyridine Carboxylates》, the research content is summarized as follows. A protocol for In and Cu co-catalyzed synthesis of a wide array of arylimidazopyridine carboxylates I [R1 = Ph, 3-thienyl, 2-naphthyl, etc.; R2 = CN, CO2Me, CO2Et, etc.; R3 = H, 8-Me, 7-OMe, etc.] by three component coupling of aryl aldehydes, malonic esters and 2-aminopyridines was described. The reaction proceeded through a reaction cascade of Knoevenagel condensation, 1,4-conjugate addition, aerobic dehydrogenation, Ortoleva-King reaction and decarboxylation. Multiple C-N and C-C bond formations in addition to multiple C-C, C-H, C-O, and N-H bond cleavages were involved in forming the product.

Product Details of C6H8N2, 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,, 1603-41-4.

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem