4-Iodo-5-pyrimidinamine is a chemical compound characterized by its pyrimidine ring structure, which is a six-membered aromatic ring containing two nitrogen atoms at positions 1 and 3. The presence of an iodine atom at the 4-position and an amino group at the 5-position contributes to its reactivity and potential applications in medicinal chemistry. This compound is typically a solid at room temperature and may exhibit properties such as solubility in polar solvents, depending on its specific functional groups. Its molecular structure suggests potential uses in the synthesis of pharmaceuticals, particularly in the development of anti-cancer or anti-viral agents, due to the biological activity often associated with pyrimidine derivatives. Additionally, the iodine substituent can enhance the compound's lipophilicity and influence its interaction with biological targets. Safety and handling precautions should be observed, as with many halogenated compounds, due to potential toxicity and environmental impact.

4-Iodo-5-pyrimidinamine

4-Iodopyrimidin-5-amine

5-PyriMidinaMine, 4-iodo-

4-Iodopyrimidin-5-amine is a stable, nitrogen containing compound that can be used as a formamide analog. It has been shown to have good solubility in water and formamide. 4-Iodopyrimidin-5-amine has also been used to study the isotopic properties of nitrogen and formamide.

CAS 942067-98-3: 4-Iodo-5-pyrimidinamine

4-Iodopyrimidin-5-amine

Ref: 10-F790822

4-Iodopyrimidin-5-amine

Ref: 54-OR345719

5-PyriMidinaMine, 4-iodo-

Ref: IN-DA00H142

4-Iodopyrimidin-5-amine

Ref: 3D-SMB06798