At 25 °C pyridine has a viscosity of 0.88 mPa/s and thermal conductivity of 0.166 W·m−1·K−1. 1603-41-4, formula is C6H8N2, Name is 2-Amino-5-methylpyridine. The enthalpy of vaporization is 35.09 kJ·mol−1 at the boiling point and normal pressure.The enthalpy of fusion is 8.28 kJ·mol−1 at the melting point. Category: pyridine-derivatives.
Kavitha, Natte;Alivelu, Munagala research published 《 The Computational Study, 3D-QSAR, and Molecular Docking Study of 2-Amino 5-Methyl Pyridine》, the research content is summarized as follows. The indeed optimized structure of the 2-Amino 5-Me Pyridine (2A5MP) and its min. energies were analyzed by using B3LYP functional with B3LYP/6-311++G (d, p) basis set. The first hyperpolarizability (β), polarizability (α), and dipole moment (μ) of the compound were computed and the results were reported. The Mulliken charges, at. polarizability tensor (APT) charges and HOMO-LUMO energy difference were calculated This energy difference illustrates the properties of optical polarizability, chem. hardness/softness, and kinetic stability/reactivity of a mol. NBO anal. was executed to know the transfer of electrons within the mol. and mol. electrostatic potential (MEP) anal. was also performed. The docking procedure was accomplished between 2- amino 5-Me pyridine and rigid protein receptors. Druglikeness principles are based on the rules of Lipinski and Veber appraise that the title mol. had the ideal physicochem. and pharmacokinetic properties to be a good drug candidate orally. The docking studies were carried out and analyzed in order to understand the binding mode of the titled compound and it was found to have a binding energy of -3.32 kcal/mol.
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,, Category: pyridine-derivatives