2-Iodo-4-methoxypyrimidine is a heterocyclic organic compound characterized by its pyrimidine ring, which is a six-membered aromatic ring containing two nitrogen atoms at the 1 and 3 positions. The presence of an iodine atom at the 2-position and a methoxy group (-OCH3) at the 4-position contributes to its unique chemical properties. This compound is typically a pale yellow to brown solid and is soluble in organic solvents such as dichloromethane and ethanol, but may have limited solubility in water. Its structure allows for potential reactivity in various chemical reactions, including nucleophilic substitutions and coupling reactions, making it valuable in medicinal chemistry and the synthesis of pharmaceuticals. The iodine substituent can enhance the compound's biological activity and facilitate further functionalization. Additionally, 2-Iodo-4-methoxypyrimidine may exhibit interesting electronic properties due to the electron-donating nature of the methoxy group and the electron-withdrawing characteristics of the iodine atom, influencing its reactivity and interactions in chemical processes.

2-Iodo-4-methoxypyrimidine

262353-35-5: 2-Iodo-4-methoxypyrimidine is a heterocyclic organic compound characterized by its pyrimidine ring, which is a six-membered aromatic ring containing two nitrogen atoms at the 1 and 3 positions. The presence of an iodine atom at the 2-position and a methoxy group (-OCH3) at the 4-position contributes to its unique chemical properties. This compound is typically a pale yellow to brown solid and is soluble in organic solvents such as dichloromethane and ethanol, but may have limited solubility in water. Its structure allows for potential reactivity in various chemical reactions, including nucleophilic substitutions and coupling reactions, making it valuable in medicinal chemistry and the synthesis of pharmaceuticals. The iodine substituent can enhance the compound's biological activity and facilitate further functionalization. Additionally, 2-Iodo-4-methoxypyrimidine may exhibit interesting electronic properties due to the electron-donating nature of the methoxy group and the electron-withdrawing characteristics of the iodine atom, influencing its reactivity and interactions in chemical processes.

CAS 262353-35-5

2-Iodo-4-methoxypyrimidine

Pyrimidine, 2-iodo-4-methoxy-

Ref: IN-DA002SDS

2-Iodo-4-methoxypyrimidine

Ref: 54-OR96389

2-Iodo-4-methoxypyrimidine

Ref: 10-F078799