4-Chloro-6-methyl-2-pyridin-4-ylpyrimidine is a heterocyclic organic compound characterized by its pyrimidine and pyridine rings, which contribute to its biological activity and chemical properties. The presence of a chlorine atom at the 4-position and a methyl group at the 6-position of the pyrimidine ring enhances its lipophilicity and potential reactivity. This compound typically exhibits a solid state at room temperature and is soluble in organic solvents, reflecting its non-polar characteristics. It is often studied for its pharmacological properties, particularly in the context of medicinal chemistry, where it may serve as a scaffold for the development of various therapeutic agents. The compound's structure allows for potential interactions with biological targets, making it of interest in drug discovery. Additionally, its stability under standard laboratory conditions and the presence of functional groups make it amenable to further chemical modifications. As with many heterocycles, it may also exhibit unique optical and electronic properties, which can be exploited in various applications, including agrochemicals and materials science.

4-chloro-6-methyl-2-pyridin-4-ylpyrimidine

61310-33-6: 4-Chloro-6-methyl-2-pyridin-4-ylpyrimidine is a heterocyclic organic compound characterized by its pyrimidine and pyridine rings, which contribute to its biological activity and chemical properties. The presence of a chlorine atom at the 4-position and a methyl group at the 6-position of the pyrimidine ring enhances its lipophilicity and potential reactivity. This compound typically exhibits a solid state at room temperature and is soluble in organic solvents, reflecting its non-polar characteristics. It is often studied for its pharmacological properties, particularly in the context of medicinal chemistry, where it may serve as a scaffold for the development of various therapeutic agents. The compound's structure allows for potential interactions with biological targets, making it of interest in drug discovery. Additionally, its stability under standard laboratory conditions and the presence of functional groups make it amenable to further chemical modifications. As with many heterocycles, it may also exhibit unique optical and electronic properties, which can be exploited in various applications, including agrochemicals and materials science.

CAS 61310-33-6

4-chloro-6-methyl-2-pyridin-4-ylpyrimidine

4-Chloro-6-methyl-2-(pyridin-4-yl)pyrimidine

Ref: 3D-LCA31033