6-Chloro-2,5-dimethyl-1H-pyrimidin-4-one is a heterocyclic organic compound characterized by its pyrimidine ring structure, which features a chlorine atom and two methyl groups as substituents. The presence of the chlorine atom at the 6-position and the methyl groups at the 2 and 5 positions contribute to its unique chemical properties, including its reactivity and potential biological activity. This compound is typically a solid at room temperature and is soluble in polar organic solvents. It may exhibit various functional properties, such as acting as a building block in the synthesis of pharmaceuticals or agrochemicals. The pyrimidine ring is known for its role in nucleic acids and can participate in hydrogen bonding, influencing its interactions in biological systems. Additionally, the compound may undergo various chemical reactions, including substitution and oxidation, making it of interest in synthetic organic chemistry. Its CAS number, 1194-73-6, serves as a unique identifier for regulatory and research purposes.

6-chloro-2,5-dimethyl-1H-pyrimidin-4-one

1194-73-6: 6-Chloro-2,5-dimethyl-1H-pyrimidin-4-one is a heterocyclic organic compound characterized by its pyrimidine ring structure, which features a chlorine atom and two methyl groups as substituents. The presence of the chlorine atom at the 6-position and the methyl groups at the 2 and 5 positions contribute to its unique chemical properties, including its reactivity and potential biological activity. This compound is typically a solid at room temperature and is soluble in polar organic solvents. It may exhibit various functional properties, such as acting as a building block in the synthesis of pharmaceuticals or agrochemicals. The pyrimidine ring is known for its role in nucleic acids and can participate in hydrogen bonding, influencing its interactions in biological systems. Additionally, the compound may undergo various chemical reactions, including substitution and oxidation, making it of interest in synthetic organic chemistry. Its CAS number, 1194-73-6, serves as a unique identifier for regulatory and research purposes.

CAS 1194-73-6

6-chloro-2,5-dimethyl-1H-pyrimidin-4-one

4(1H)-Pyrimidinone, 6-chloro-2,5-dimethyl-

Ref: IN-DA000IPJ

4-Chloro-5-iodo-6-hydroxy-2-methylpyrimidine

Ref: 54-OR43601

6-Chloro-5-iodo-2-methyl-4-pyrimidinol

Ref: 3D-BAA19473