2,4-Diamino-5-iodoquinazoline is a chemical compound characterized by its quinazoline core, which is a bicyclic structure containing two nitrogen atoms. This compound features two amino groups at the 2 and 4 positions and an iodine atom at the 5 position of the quinazoline ring. It is typically a solid at room temperature and may exhibit moderate solubility in polar solvents due to the presence of amino groups, which can engage in hydrogen bonding. The iodine substituent can influence the compound's reactivity and biological activity, potentially making it a candidate for various pharmaceutical applications. Its structure suggests potential use in medicinal chemistry, particularly in the development of compounds targeting specific biological pathways. As with many nitrogen-containing heterocycles, it may exhibit interesting electronic properties and could participate in various chemical reactions, including nucleophilic substitutions and coupling reactions. Safety and handling precautions should be observed, as with any chemical compound, particularly those with halogen substituents.

2 4-DIAMINO-5-IODOQUINAZOLINE

119584-76-8: 2,4-Diamino-5-iodoquinazoline is a chemical compound characterized by its quinazoline core, which is a bicyclic structure containing two nitrogen atoms. This compound features two amino groups at the 2 and 4 positions and an iodine atom at the 5 position of the quinazoline ring. It is typically a solid at room temperature and may exhibit moderate solubility in polar solvents due to the presence of amino groups, which can engage in hydrogen bonding. The iodine substituent can influence the compound's reactivity and biological activity, potentially making it a candidate for various pharmaceutical applications. Its structure suggests potential use in medicinal chemistry, particularly in the development of compounds targeting specific biological pathways. As with many nitrogen-containing heterocycles, it may exhibit interesting electronic properties and could participate in various chemical reactions, including nucleophilic substitutions and coupling reactions. Safety and handling precautions should be observed, as with any chemical compound, particularly those with halogen substituents.

CAS 119584-76-8

2 4-DIAMINO-5-IODOQUINAZOLINE

5-Iodoquinazoline-2,4-diamine

Ref: IN-DA000IZN

2,4-Diamino-5-iodoquinazoline

Ref: 54-OR0084