30152-85-3

Upstream product

• 2050-85-3 N,N'-(o-phenylene)di(acetamide) 
• 75-36-5 acetyl chloride 
• 99-56-9 4-Nitrophenylene-1,2-diamine 
• 34801-09-7 N-(2-aminophenyl)acetamide 
• 552-32-9 o-nitroacetanilide 

Downstream Products

• 1792-40-1 2-methyl-5-nitrobenzimidazole 
• 22177-15-7 1,2,4-triaminobenzene N¹,N²-diacetate 
• 80825-68-9 N,N'-diacetyl-4,5-dinitro-1,2-phenylenediamine 
• 80825-71-4 N-acetyl-2-nitroamino-4,5-dinitroaniline 
• 80825-69-0 N,N'-diacetyl-2-nitroamino-4,5-dinitroaniline 
• 80825-70-3 ammonium salt of N-acetyl-2-nitroamino-4,5-dinitroaniline 
• 22177-17-9 N,N'-{4-[bis(2-hydroxyethyl)amino]-1,2-phenylene}bis[acetamide] 
• 326833-27-6 2-methyl-1-[(4-methylphenyl)sulfonyl]-5-(tetrahydro-2H-1,4-selenazin-4-yl)-1H-benzimidazole 
• 326833-28-7 2-methyl-1-[(4-methylphenyl)sulfonyl]-6-(tetrahydro-2H-1,4-selenazin-4-yl)-1H-benzimidazole 
• 326833-26-5 2,2'-{{2-methyl-1-[(4-methylphenyl)sulfonyl]-1H-benzimidazol-6-yl}imino}bis[ethanol] bis(4-methylbenzenesulfonate) 
• 326833-25-4 2,2'-{{2-methyl-1-[(4-methylphenyl)sulfonyl]-1H-benzimidazol-5-yl}imino}bis[ethanol] 
• 30120-73-1 1,2,4-triaminobenzene N¹,N²,N⁴-triacetate 
• 56842-62-7 5-acetamido-2-methylbenzimidazole 

Relevant academic research and scientific papers

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

SYNTHESIS AND TRANSFORMATION OF NITRO-N,N'-DIACETYLPHENYLENEDIAMINES

N,N'-Diacetyl-2,3-dinitro-1,4-phenylenediamine, N,N'-diacetyl-2,3-dinitro-4-nitroaminoaniline, and 1,4-bis(acetylnitroamino)-2,3-dinitrobenzene were obtained by nitration of N,N'-diacetyl-1,4-phenylenediamine by solutions of nitric acid in acetic acid or acetic anhydride.In nucleophilic substitution reactions the obtained N-nitroanilines eliminate the N-nitro group or acetyl group, depending on the nature of the nucleophile, to form the salts of the corresponding N-nitroamines.