In contrast to benzene, Pyridine’s electron density is not evenly distributed over the ring, reflecting the negative inductive effect of the nitrogen atom. 1603-41-4, formula is C6H8N2, Name is 2-Amino-5-methylpyridine. For this reason, pyridine has a dipole moment and a weaker resonant stabilization than benzene (resonance energy 117 kJ·mol−1 in pyridine vs. 150 kJ·mol−1 in benzene). Product Details of C6H8N2.
Mishra, Mitali;Mishra, Nilima P.;Raiguru, Bishnu P.;Das, Tapaswini;Mohapatra, Seetaram;Nayak, Sabita;Mishra, Deepak R.;Panda, Jasmine;Sahoo, Dipak K. research published 《 Microwave-Assisted Iron(III)Chloride Catalyzed One-Pot Michael Addition-Cyclization for the Synthesis of 6H-Chromeno[4′,3′:4,5] imidazo[1,2-a]pyridine》, the research content is summarized as follows. An efficient one-pot Michael addition-cyclization reaction wa developed for the synthesis of 6H-chromeno[4′,3′ : 4,5]imidazo[1,2-a]pyridine under microwave irradiation method. The current protocol paved the way for the synthesis of twenty number of structurally diversified imidazo[1,2-a]pyridines in high yield by the reaction of substituted 2-aryl-3-nitro-2H-chromenes with 2-aminopyridines using anhydrous iron(III)chloride. This current protocol was the first report of the preparation of this medicinally significant highly substituted 6H-chromeno[4′,3′ : 4,5]imidazo[1,2-a]pyridine derivatives under microwave irradiation in good to high yields. The tolerance of a wide range of functional groups, operational simplicity and short reaction times were the significant advantages of this protocol.
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,, Product Details of C6H8N2