17816-43-2

Basic information

• Product Name: 3a,6a-di-(4-methoxyphenyl)tetrahydroimidazo<4,5-d>imidazole-2,5-dione
• CAS NO: 17816-43-2
• Molecular Weight: 354.365
• Mol File: 17816-43-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 3a,6a-di-(4-methoxyphenyl)tetrahydroimidazo<4,5-d>imidazole-2,5-dione(CAS DataBase Reference)
• NIST Chemistry Reference: 3a,6a-di-(4-methoxyphenyl)tetrahydroimidazo<4,5-d>imidazole-2,5-dione(17816-43-2)
• EPA Substance Registry System: 3a,6a-di-(4-methoxyphenyl)tetrahydroimidazo<4,5-d>imidazole-2,5-dione(17816-43-2)

Safety Data

• Hazardous Substances Data: 17816-43-2(Hazardous Substances Data)

Upstream product

• 1226-42-2 1,2-bis(4-methoxyphenyl)-1,2-ethanedione 
• 57-13-6 urea 

Downstream Products

• 663908-80-3 13b,13c-bis(4-methoxyphenyl)-5,7,12,13b,13c,14-hexahydro-5a,6a,12a,13a-tetraazabenzo[5,6]azuleno[2,1,8-ija]benzo[f]azulene-6,13-dione 

Relevant articles and documents

Condensation reactions of benzils with ureas in ethylene glycol

Reactions of benzils and urea in ethylene glycol at 180° for 1-2 hours gave 2,4,5-triaryloxazoles as major products and bicyclic imidazoimidazole-2,5-diones as minor products. N-Methylurea and W-phenylurea gave the oxazoles under similar conditions. The solvent seemed to assist the formation of oxazole by eliminating the isocyanate components as ethylene glycol biscarbamates.