4,6-Pyrimidinediamine, 5-iodo- is a chemical compound characterized by its pyrimidine ring structure, which features two amino groups at the 4 and 6 positions and an iodine atom at the 5 position. This compound is typically a solid at room temperature and is soluble in polar solvents due to the presence of amino groups that can engage in hydrogen bonding. The iodine substituent can influence the compound's reactivity and biological activity, making it of interest in medicinal chemistry and material science. It may exhibit properties such as antimicrobial or antitumor activity, depending on its specific interactions within biological systems. The presence of the amino groups allows for potential derivatization, which can enhance its utility in various applications, including pharmaceuticals and agrochemicals. As with many nitrogen-containing heterocycles, it may also participate in various chemical reactions, such as nucleophilic substitutions or coupling reactions, making it a versatile building block in organic synthesis. Safety data should be consulted for handling and storage, as with any chemical substance.

4,6-Pyrimidinediamine, 5-iodo-

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5-Iodopyrimidine-4,6-diamine

4,6-Diamino-5-iodopyrimidine is a synthetic chemical compound. It is the cyclization product of the reaction of 2,4,6-trichloroacetophenone and acetamide. This compound has been used as a cross-coupling reaction intermediate for the synthesis of pyridines and quinolines. 4,6-Diamino-5-iodopyrimidine can be used as an intramolecular cyclization reagent to form triaryl compounds with arylated or diarylated aryl groups. 4,6-Diamino-5-iodopyrimidine has also been used in the preparation of polymers such as poly(vinyl alcohol) and poly(vinyl acetate).

CAS 214907-09-2: 4,6-Pyrimidinediamine, 5-iodo-

5-Iodopyrimidine-4,6-diamine

Ref: 10-F339876

4,6-Diamino-5-iodopyrimidine

Ref: 3D-FD33766

5-Iodopyrimidine-4,6-diamine

Ref: IN-DA00715N