34489-87-7

Upstream product

• 615-43-0 2-iodophenylamine 
• 610-14-0 2-nitrobenzyl chloride 
• 552-16-9 ortho-nitrobenzoic acid 

Downstream Products

• 898806-32-1 N-benzyl-N-(2-iodophenyl)-2-nitrobenzamide 
• 898806-33-2 N-ethyl-N-(2-iodophenyl)-2-nitrobenzamide 
• 826991-63-3 N-(2-iodo-phenyl)-N-methyl-2-nitro-benzamide 
• 826991-72-4 2-amino-N-(2-iodo-phenyl)-N-(2-dimethylamino-ethyl)-benzamide 
• 13137-17-2 10-(2-dimethylamino-ethyl)-5,10-dihydro-dibenzo[b,e][1,4]diazepin-11-one 
• 32047-69-1 10-methyl-5,10-dihydro-dibenzo[b,e][1,4]diazepin-11-one 
• 826991-64-4 N-(2-iodo-phenyl)-N-(2-dimethylamino-ethyl)-2-nitro-benzamide 
• 826991-71-3 2-amino-N-(2-iodo-phenyl)-N-methyl-benzamide 
• 898806-46-7 2-benzamido-N-(2-iodophenyl)-N-methylbenzamide 
• 898806-43-4 N-ethyl-N-(2-iodophenyl)-2-(2-nitrobenzamido)benzamide 
• 898806-41-2 N-(2-iodophenyl)-N-methyl-2-(2-nitrobenzamido)benzamide 
• 898806-39-8 N-benzyl-N-(2-iodophenyl)-2-(2-nitrobenzamido)benzamide 
• 898806-36-5 N-benzyl-N-(2-iodophenyl)-2-(2-iodobenzamido)benzamide 
• 898806-35-4 2-amino-N-ethyl-N-(2-iodophenyl)benzamide 

Relevant academic research and scientific papers

Contrasting three-dimensional frame-work structures in the isomeric pair 2-iodo-N-(2-nitrophenyl)benzamide and N-(2-iodophenyl)-2-nitrobenzamide

In 2-iodo-N-(2-nitrophenyl)benzamide, C13H9IN 2O3, the molecules are linked into a three-dimensional framework structure by a combination of a C-H...O hydrogen bond, and iodo-nitro, carbonyl-carbonyl and aromati

Copper-Catalyzed Domino Reaction Involving Nitro as an Unexpected Leaving Group: Construction of Dibenzo-Fused Azepinone Ring

A copper-catalyzed new domino reaction allowed the facile and direct construction of the dibenzo-fused azepinone ring leading to an array of novel small molecules. The co-catalyst, ligand or additive free one-pot method afforded a unique class of function

Conformational communication between the Ar-CO and Ar-N axes in 2,2′-disubstituted benzanilides and their derivatives

Benzanilides containing two or more potentially stereogenic amide axes exist in solution as mixtures of conformers which are detectable by NMR. For simple tertiary benzanilides carrying an ortho substituent on each ring, conformational control can be high

Palladium-mediated approach to dibenzo[b,e][1,4]diazepines and benzopyrido-analogues. An efficient synthesis of tarpane

An original synthetic route toward dibenzo[b,e][1,4]diazepin-11-ones and analogues pyridobenzodiazepinones has been developed. The method relies upon an intramolecular amination process between an (hetero)aryl halide and the appropriate aniline moiety. Graphical Abstract.