5-Pyridin-2-ylpyrimidine is a heterocyclic organic compound characterized by its dual ring structure, which includes a pyridine and a pyrimidine moiety. The presence of the pyridine ring, which is a six-membered aromatic ring containing one nitrogen atom, contributes to its basicity and potential for forming coordination complexes. The pyrimidine ring, a six-membered ring containing two nitrogen atoms at positions 1 and 3, is known for its role in various biological systems, particularly in nucleic acids. This compound is typically a solid at room temperature and may exhibit moderate solubility in polar organic solvents. Its chemical properties are influenced by the electron-withdrawing nature of the nitrogen atoms, which can affect reactivity and interactions with other molecules. 5-Pyridin-2-ylpyrimidine is of interest in medicinal chemistry and drug development, as it may exhibit biological activity, including potential anti-cancer or anti-inflammatory properties. As with many heterocycles, its reactivity can be tailored through substitution at various positions on the rings, allowing for the design of derivatives with specific functions.

5-pyridin-2-ylpyrimidine

64858-29-3: 5-Pyridin-2-ylpyrimidine is a heterocyclic organic compound characterized by its dual ring structure, which includes a pyridine and a pyrimidine moiety. The presence of the pyridine ring, which is a six-membered aromatic ring containing one nitrogen atom, contributes to its basicity and potential for forming coordination complexes. The pyrimidine ring, a six-membered ring containing two nitrogen atoms at positions 1 and 3, is known for its role in various biological systems, particularly in nucleic acids. This compound is typically a solid at room temperature and may exhibit moderate solubility in polar organic solvents. Its chemical properties are influenced by the electron-withdrawing nature of the nitrogen atoms, which can affect reactivity and interactions with other molecules. 5-Pyridin-2-ylpyrimidine is of interest in medicinal chemistry and drug development, as it may exhibit biological activity, including potential anti-cancer or anti-inflammatory properties. As with many heterocycles, its reactivity can be tailored through substitution at various positions on the rings, allowing for the design of derivatives with specific functions.

CAS 64858-29-3

5-pyridin-2-ylpyrimidine

5-(2-Pyridinyl)pyrimidine

Ref: IN-DA00EKY6

5-Pyridin-2-yl-pyrimidine

Ref: 10-F200920