857088-45-0

Upstream product

• 299173-24-3 [3-iodo-4-(methoxycarbonyl)]benzoic acid 
• 60728-41-8 1-methyl-2-aminoterephthalate 

Downstream Products

• 857088-46-1 N⁴-[2-(2-chlorophenyl)ethyl]-2-iodoterephthalamide 
• 857088-47-2 N⁴-(3-ethoxypropyl)-2-iodoterephthalamide 
• 857088-50-7 tert-butyl 1-[4-(aminocarbonyl)-3-iodobenzoyl]-L-prolinate 
• 1314804-26-6 3-diphenylphosphoryl-4-(aminocarbonyl)benzoic acid 
• 857088-52-9 N⁴-[2-(3,4-dichlorophenyl)ethyl]-2-iodoterephthalamide 
• 857088-51-8 tert-butyl N-[4-(aminocarbonyl)-3-iodobenzoyl]-O-tert-butyl-L-allothreoninate 
• 857088-48-3 tert-butyl N²-[4-(aminocarbonyl)-3-iodobenzoyl]-N⁵-[{[(2,2,5,7,8-pentamethylchroman-6-yl)sulfonyl]amino}(imino)mehtyl]-L-ornithinate 

Relevant academic research and scientific papers

Rapid and selective nitroxyl (HNO) trapping by phosphines: Kinetics and new aqueous ligations for HNO detection and quantitation

Recent studies distinguish the biological and pharmacological effects of nitroxyl (HNO) from its oxidized/deprotonated product nitric oxide (?NO), but the lack of HNO detection methods limits the understanding its in vivo mechanisms and the identification

Novel α,α-difluorohomophthalimides via copper-catalyzed tandom cross-coupling-cyclization of 2-halobenzamides with α,α-difluoro reformatskii reagent

Novel α,α-difluorohomophthalimides 2 were prepared by reacting N-substituted 2-halobenzamides with the α,α-difluoro Reformatskii reagent BrZnCF2CO2Et (3) in the presence of CuBr at room temperature. The synthesis involves a CuBr-medi