22177-15-7

Upstream product

• 30152-85-3 N,N'-diacetyl-4-nitro-1,2-phenylenediamine 
• 34801-09-7 N-(2-aminophenyl)acetamide 
• 2050-85-3 N,N'-(o-phenylene)di(acetamide) 
• 552-32-9 o-nitroacetanilide 
• 99-56-9 4-Nitrophenylene-1,2-diamine 

Downstream Products

• 30120-73-1 1,2,4-triaminobenzene N¹,N²,N⁴-triacetate 
• 56842-62-7 5-acetamido-2-methylbenzimidazole 
• 326833-25-4 2,2'-{{2-methyl-1-[(4-methylphenyl)sulfonyl]-1H-benzimidazol-5-yl}imino}bis[ethanol] 
• 326833-26-5 2,2'-{{2-methyl-1-[(4-methylphenyl)sulfonyl]-1H-benzimidazol-6-yl}imino}bis[ethanol] bis(4-methylbenzenesulfonate) 
• 326833-28-7 2-methyl-1-[(4-methylphenyl)sulfonyl]-6-(tetrahydro-2H-1,4-selenazin-4-yl)-1H-benzimidazole 
• 326833-27-6 2-methyl-1-[(4-methylphenyl)sulfonyl]-5-(tetrahydro-2H-1,4-selenazin-4-yl)-1H-benzimidazole 
• 22177-17-9 N,N'-{4-[bis(2-hydroxyethyl)amino]-1,2-phenylene}bis[acetamide] 

Relevant academic research and scientific papers

Generation of Cu nanoparticles on novel designed Fe3O4@SiO2/EP.EN.EG as reusable nanocatalyst for the reduction of nitro compounds

In this work, copper nanoparticles loaded on Fe3O4@SiO2, which we have named Fe3O4@SiO2/EP.EN.EG@Cu for short, have been designed, prepared and characterized by XRD, FTIR, TEM, SEM, EDS, TGA, ICP, successfully. The catalytic performance was investigated in the reduction of aromatic nitro compounds in the presence of NaBH4 aqueous solution as the source of hydrogen at 50°C. The Fe3O4@SiO2/EP.EN.EG@Cu catalyst was readily removed from the reaction mixture by applying an external magnet and reused for five times without significant loss of catalytic activity.

Labelling of carbaboranyl compounds with a selenium atom with a view to applications in boron-neutron-capture therapy (BNCT) and positron-emission tomography (PET)

We synthesized 2′-carbaboranyl-2.5′-bi-1H-benzimidazoles containing 10 B-atoms and labeled with Se or the positron-emitting radionuclide 73Se (I1/2=7.1 h). with a view to their application to cancer treatment by boron-neutron-capture