1352820-89-3

Basic information

• Product Name: 5-phenyl-5H-benzo[d]benzo[4,5]imidazo[1,2-a]imidazole
• Synonyms: 5-phenyl-5H-benzo[d]benzo[4,5]imidazo[1,2-a]imidazole
• CAS NO: 1352820-89-3
• Molecular Weight: 283.332
• Mol File: 1352820-89-3.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: 5-phenyl-5H-benzo[d]benzo[4,5]imidazo[1,2-a]imidazole(CAS DataBase Reference)
• NIST Chemistry Reference: 5-phenyl-5H-benzo[d]benzo[4,5]imidazo[1,2-a]imidazole(1352820-89-3)
• EPA Substance Registry System: 5-phenyl-5H-benzo[d]benzo[4,5]imidazo[1,2-a]imidazole(1352820-89-3)

Safety Data

• Hazardous Substances Data: 1352820-89-3(Hazardous Substances Data)

Upstream product

• 1560667-91-5 2-bromo-N-(((2-iodophenyl)imino)methylene)aniline 
• 62-53-3 aniline 
• 101-01-9 N,N',N''-triphenylguanidine 
• 108-86-1 bromobenzene 
• 26268-23-5 2‐(1H‐benzo[d]imidazol‐1‐yl)aniline 
• 769968-48-1 N,N'-di-ortho-iodophenylcarbodiimide 
• 94-02-0 ethyl 3-oxo-3-phenylpropionate 
• 1493-27-2 ortho-nitrofluorobenzene 
• 25688-28-2 1‐(2‐nitrophenyl)‐1H‐benzo[d]imidazole 
• 1352820-61-1 2-(1H-benzo[d]imidazol-1-yl)-N-phenylaniline 
• 51-17-2 benzoimidazole 
• 591-50-4 iodobenzene 
• 28890-99-5 benzimidazolo<1,2-a>benzimidazole 

Downstream Products

• 1537905-34-2 2-iodo-5-phenyl-5H-benzo[d]benzo[4,5]imidazo[1,2-a]imidazole 
• 1537904-98-5 C₃₁H₂₀N₄ 
• 1537905-21-7 C₄₄H₂₇N₇ 
• 1537905-19-3 C₃₂H₂₀N₆ 
• 1537905-20-6 C₃₇H₂₄N₄ 

Relevant articles and documents

Synthesis of a tetracyclic aminobenzimidazole derivative via tandem cyclization of triphenylguanidine

We developed a new reaction for the one-pot synthesis of a fused cyclic compound from triphenylguanidine, which was thought to be tandem cyclization, with a moderate yield. In this reaction, conditions such as the metal reagent, oxidant, solvent, and liga

An efficient and facile synthesis of benzimidazo[1,2-a]benzimidazoles via copper-catalyzed domino addition/double cyclization

A copper-catalyzed synthesis of benzimidazo[1,2-a]benzimidazoles by domino addition/double cyclization of bis-(o-haloaryl)carbodiimides with primary amines was developed. A variety of the desired polycyclic benzimidazoles were efficiently and facilely assembled. Multibonds and polycyclic moieties were directly constructed in one pot. 2-Bromo-2′-iodo-diarylcarbodiimides gave good selectivity. This journal is the Partner Organisations 2014.

Copper-catalyzed domino addition/double cyclization: An approach to polycyclic benzimidazole derivatives

An efficient and versatile method for the assembly of novel polycyclic benzimidazole derivatives has been developed by Cu-catalyzed domino addition/double cyclization reactions. A wide variety of polycyclic benzimidazole derivatives, which might be used as synthetic medicines and functional materials, were successfully assembled from bis-(o-haloaryl) carbodiimides. Unexpected N-methylated benzo[4,5]imidazo[1,2-a]indoles can also be selectively assembled. Multibonds and polycyclic moieties were conveniently formed in one pot during these domino processes.