88406-62-6

Basic information

• Product Name: N-{[N'-(4-Chloro-phenyl)-guanidino]-imino-methyl}-2-[2-[N'-(4-chloro-phenyl)-guanidino]-5-oxo-3,5-dihydro-imidazol-(4Z)-ylidene]-acetamide
• CAS NO: 88406-62-6
• Molecular Weight: 501.335
• Mol File: 88406-62-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N-{[N'-(4-Chloro-phenyl)-guanidino]-imino-methyl}-2-[2-[N'-(4-chloro-phenyl)-guanidino]-5-oxo-3,5-dihydro-imidazol-(4Z)-ylidene]-acetamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-{[N'-(4-Chloro-phenyl)-guanidino]-imino-methyl}-2-[2-[N'-(4-chloro-phenyl)-guanidino]-5-oxo-3,5-dihydro-imidazol-(4Z)-ylidene]-acetamide(88406-62-6)
• EPA Substance Registry System: N-{[N'-(4-Chloro-phenyl)-guanidino]-imino-methyl}-2-[2-[N'-(4-chloro-phenyl)-guanidino]-5-oxo-3,5-dihydro-imidazol-(4Z)-ylidene]-acetamide(88406-62-6)

Safety Data

• Hazardous Substances Data: 88406-62-6(Hazardous Substances Data)

Upstream product

• 762-42-5 dimethyl acetylenedicarboxylate 
• 5304-59-6 4-chlorophenylbiguanide 

Relevant articles and documents

Reaction of Biguanides and Related Compounds. XV. Cyclizations of Arylbiguanides and 2-Guanidinobenzimidazole with Bifunctional Unsaturated Dicarboxylates to s-Triazines and Imidazolines

Arylbiguanide (1) and 2-guanidinobenzimidazole (2) were reacted with diethyl azodicarboxylate (3) to give dihydro-s-triazine (6) and dihydrobenzimidazol-s-triazine (9), respectively.The reaction of 1 and 2 with dimethyl acetylenedicarboxylate (4) in alcohol provided the corresponding imidazolinylideneacetylguanidines (10 and 12), which were converted to alkyl imidazolidinylideneacetates (11 and 13) by alcoholysis.The compounds 10 and 12 underwent acid-catalyzed ring conversion to pyrimidine compounds (15 and 16).Keywords - arylbiguanide; guanidinobenzimidazole; diethyl azodicarboxylate; dimethyl acetylenedicarboxylate; s-triazine; imidazoline; cyclization; ring conversion