1,3,4,6-Tetrachlorotetrahydroimidazo(4,5-d)imidazole-2,5(1H,3H)-dione(CAS: 776-19-2)

1,3,4,6-Tetrachlorotetrahydroimidazo(4,5-d)imidazole-2,5(1H,3H)-dione (CAS: 776-19-2) crystallizes in a solid form. Its molecular weight is approximately 302.01 g/mol. It has a low solubility in water but is soluble in common organic solvents like chloroform and acetonitrile. This compound is highly reactive with halogenated compounds and is prone to hydrolysis under basic conditions. It is a potent reagent in organic synthesis due to its strong electrophilic character.

1,3,4,6-Tetrachlorotetrahydroimidazo(4,5-d)imidazole-2,5(1H,3H)-dione (CAS: 776-19-2) is commonly synthesized via a multi-step process involving the condensation of 1,3-dichloro-4,6-dichloro-2,5-imidazolidinedione with chlorine gas. The reaction is carried out in the presence of a suitable catalyst and under anhydrous conditions to ensure high selectivity and yield. Common solvents used include acetonitrile and chloroform.

1,3,4,6-Tetrachlorotetrahydroimidazo(4,5-d)imidazole-2,5(1H,3H)-dione (CAS: 776-19-2) is primarily used in pharmaceuticals for the synthesis of certain organic compounds. It also finds applications in the polymer industry as a cross-linking agent, in the production of sensors for detecting halogen compounds, and in the semiconductor industry for specific chemical processes.

When handling 1,3,4,6-Tetrachlorotetrahydroimidazo(4,5-d)imidazole-2,5(1H,3H)-dione (CAS: 776-19-2), ensure the use of personal protective equipment (PPE) including gloves, goggles, and a lab coat. Store it in a cool, dry place away from direct sunlight and combustible materials. Work under a fume hood to minimize exposure to vapors. In case of a spill, clean up with appropriate absorbent materials and follow the instructions in the safety data sheet (SDS).