5-Fluoro-2,4-dimethoxypyrimidine is a heterocyclic organic compound characterized by a pyrimidine ring substituted with a fluorine atom and two methoxy groups. The presence of the fluorine atom at the 5-position enhances its biological activity and lipophilicity, making it of interest in pharmaceutical research. The methoxy groups at the 2 and 4 positions contribute to the compound's overall polarity and can influence its reactivity and solubility in various solvents. This compound typically appears as a white to off-white solid and is soluble in organic solvents like methanol and ethanol. Its molecular structure allows for potential interactions with biological targets, making it relevant in the development of agrochemicals and medicinal compounds. Additionally, the compound's stability and reactivity can be influenced by the electronic effects of the substituents, which may affect its synthesis and application in various chemical reactions. Overall, 5-fluoro-2,4-dimethoxypyrimidine is a significant compound in the field of organic chemistry and drug development.

5-fluoro-2,4-dimethoxypyrimidine

4330-22-7: 2,4-Dimethoxy-5-fluoropyrimidine, NSC 109178, Pyrimidine, 5-fluoro-2,4-dimethoxy-, T6N Cnj Bo1 Do1 Ef [Wln]

5-Fluoro-2,4-dimethoxypyrimidine

5-fluoro-2,4-dimethoxy-pyrimidine

5-Fluoro-2,4-dimethoxypyrimidine is a chemical compound with the molecular formula C6H6FN3O2. The compound exists in three tautomeric forms. It is a weak base that can be protonated to form the hydrogen bonded anion or deprotonated to form the zwitterionic cation. 5-Fluoro-2,4-dimethoxypyrimidine has been shown to stabilize the equilibrium between its tautomers. This property is due to its conjugated system and strong hydrogen bonding capabilities.

CAS 4330-22-7: 5-fluoro-2,4-dimethoxypyrimidine

5-Fluoro-2,4-dimethoxypyrimidine

Ref: 54-PC100990

5-fluoro-2,4-dimethoxy-pyrimidine

Ref: IN-DA00745R

5-fluoro-2,4-dimethoxypyrimidine

Ref: 10-F370054

5-Fluoro-2,4-Dimethoxypyrimidine

Ref: 3D-FF80346