3-Chloro-5-methoxy-4-methylpyridine is a heterocyclic organic compound characterized by a pyridine ring substituted with a chlorine atom, a methoxy group, and a methyl group. The presence of the chlorine atom at the 3-position introduces a polar functional group, which can influence the compound's reactivity and solubility in various solvents. The methoxy group at the 5-position enhances the electron-donating properties of the molecule, potentially affecting its interaction with other chemical species. The methyl group at the 4-position contributes to the overall hydrophobic character of the compound. This compound may exhibit biological activity, making it of interest in pharmaceutical research. Its structural features suggest potential applications in the synthesis of more complex molecules or as a building block in organic synthesis. Additionally, the compound's stability and reactivity can be influenced by the electronic effects of the substituents on the pyridine ring, which may also affect its behavior in various chemical reactions.

3-chloro-5-methoxy-4-methylpyridine

1261488-20-3: 3-Chloro-5-methoxy-4-methylpyridine is a heterocyclic organic compound characterized by a pyridine ring substituted with a chlorine atom, a methoxy group, and a methyl group. The presence of the chlorine atom at the 3-position introduces a polar functional group, which can influence the compound's reactivity and solubility in various solvents. The methoxy group at the 5-position enhances the electron-donating properties of the molecule, potentially affecting its interaction with other chemical species. The methyl group at the 4-position contributes to the overall hydrophobic character of the compound. This compound may exhibit biological activity, making it of interest in pharmaceutical research. Its structural features suggest potential applications in the synthesis of more complex molecules or as a building block in organic synthesis. Additionally, the compound's stability and reactivity can be influenced by the electronic effects of the substituents on the pyridine ring, which may also affect its behavior in various chemical reactions.

CAS 1261488-20-3

3-chloro-5-methoxy-4-methylpyridine