6-Chloro-3-cyclohexylpyrimidine-2,4(1H,3H)-dione is a heterocyclic organic compound characterized by its pyrimidine ring structure, which is substituted at the 6-position with a chlorine atom and at the 3-position with a cyclohexyl group. This compound features two carbonyl groups at the 2 and 4 positions of the pyrimidine ring, contributing to its diketone functionality. The presence of the cyclohexyl group enhances its lipophilicity, potentially influencing its biological activity and solubility properties. The chlorine substituent can also affect the compound's reactivity and interaction with biological targets. Typically, compounds of this nature may exhibit pharmacological properties, making them of interest in medicinal chemistry. The molecular structure suggests potential applications in drug development, particularly in areas requiring modulation of biological pathways. As with many heterocycles, the stability and reactivity of this compound can be influenced by the electronic effects of the substituents and the overall molecular conformation.

6-chloro-3-cyclohexylpyrimidine-2,4(1H,3H)-dione

34654-87-0: 6-Chloro-3-cyclohexylpyrimidine-2,4(1H,3H)-dione is a heterocyclic organic compound characterized by its pyrimidine ring structure, which is substituted at the 6-position with a chlorine atom and at the 3-position with a cyclohexyl group. This compound features two carbonyl groups at the 2 and 4 positions of the pyrimidine ring, contributing to its diketone functionality. The presence of the cyclohexyl group enhances its lipophilicity, potentially influencing its biological activity and solubility properties. The chlorine substituent can also affect the compound's reactivity and interaction with biological targets. Typically, compounds of this nature may exhibit pharmacological properties, making them of interest in medicinal chemistry. The molecular structure suggests potential applications in drug development, particularly in areas requiring modulation of biological pathways. As with many heterocycles, the stability and reactivity of this compound can be influenced by the electronic effects of the substituents and the overall molecular conformation.

CAS 34654-87-0

6-chloro-3-cyclohexylpyrimidine-2,4(1H,3H)-dione

6-Chloro-3-cyclohexyl-1,2,3,4-tetrahydropyrimidine-2,4-dione

Ref: 3D-JBA65487