1379803-65-2

Upstream product

• 2613-27-6 1-nitro-4-(pentafluorosulfanyl)benzene 

Downstream Products

• 1379803-57-2 2-(2-bromophenyl)-5-pentafluorosulfanyl-1H-benzoimidazole 
• 1379803-58-3 2-(3-bromophenyl)-5-pentafluorosulfanyl-1H-benzoimidazole 
• 1379803-59-4 2-(4-methoxyphenyl)-5-pentafluorosulfanyl-1H-benzoimidazole 
• 1379803-60-7 2-ethyl-5-pentafluorosulfanyl-1H-benzoimidazole 
• 1211526-90-7 5-pentafluorosulfanyl-1,3-dihydrobenzoimidazole-2-thione 
• 1379803-63-0 2,3-diphenyl-6-(pentafluorosulfanyl)quinoxaline 
• 1379803-64-1 5-pentafluorosulfanyl-1H-benzotriazole 
• 663179-60-0 5-pentafluorosulfanyl-1H-benzoimidazole 
• 1379803-56-1 2-(4-chlorophenyl)-5-pentafluorosulfanyl-1H-benzoimidazole 
• 663179-59-7 4-pentafluorosulfanyl-1,2-phenylenediamine 

Relevant academic research and scientific papers

Direct amination of nitro(pentafluorosulfanyl)benzenes through vicarious nucleophilic substitution of hydrogen

1-Nitro-4-(pentafluorosulfanyl)benzene underwent direct amination with 1,1,1-trimethylhydrazinium iodide in the presence of tBuOK in DMSO to give 2-nitro-5-(pentafluorosulfanyl)aniline in good yield. 1-Nitro-3- (pentafluorosulfanyl)benzene, under similar

Synthesis of aliphatic sulfur pentafluorides by oxidation of SF5-containing anisole, phenols, and anilines

4-(Pentafluorosulfanyl)catechol, 2-amino-4-(pentafluorosulfanyl)phenol, and 2-amino-5-(pentafluorosulfanyl) phenol undergo oxidation by lead tetraacetate at ambient temperature leading to dearomatization and the formation of SF5-substituted nit