5-Iodo-2,6-dimethylpyrimidin-4(1H)-one is a heterocyclic organic compound characterized by its pyrimidine ring structure, which contains nitrogen atoms at positions 1 and 3. The presence of an iodine atom at the 5-position and two methyl groups at the 2 and 6 positions contributes to its unique chemical properties. This compound typically exhibits a solid state at room temperature and is soluble in polar organic solvents. It may participate in various chemical reactions, including nucleophilic substitutions and electrophilic aromatic substitutions, due to the reactivity of the iodine substituent and the electron-donating nature of the methyl groups. The compound's structure suggests potential applications in pharmaceuticals and agrochemicals, particularly as a building block in the synthesis of biologically active molecules. Additionally, its stability and reactivity can be influenced by the presence of functional groups and the overall electronic environment of the pyrimidine ring. As with many halogenated compounds, safety precautions should be taken when handling this substance due to potential toxicity and environmental impact.

5-iodo-2,6-dimethylpyrimidin-4(1H)-one

83410-37-1: 5-Iodo-2,6-dimethylpyrimidin-4(1H)-one is a heterocyclic organic compound characterized by its pyrimidine ring structure, which contains nitrogen atoms at positions 1 and 3. The presence of an iodine atom at the 5-position and two methyl groups at the 2 and 6 positions contributes to its unique chemical properties. This compound typically exhibits a solid state at room temperature and is soluble in polar organic solvents. It may participate in various chemical reactions, including nucleophilic substitutions and electrophilic aromatic substitutions, due to the reactivity of the iodine substituent and the electron-donating nature of the methyl groups. The compound's structure suggests potential applications in pharmaceuticals and agrochemicals, particularly as a building block in the synthesis of biologically active molecules. Additionally, its stability and reactivity can be influenced by the presence of functional groups and the overall electronic environment of the pyrimidine ring. As with many halogenated compounds, safety precautions should be taken when handling this substance due to potential toxicity and environmental impact.

CAS 83410-37-1

5-iodo-2,6-dimethylpyrimidin-4(1H)-one

5-Iodo-2,6-dimethylpyrimidin-4-ol

Ref: IN-DA004RTH

5-Iodo-2,6-dimethylpyrimidin-4-ol

Ref: 10-F235381