45860-18-2

Upstream product

• 147-82-0 2,4,6-tribromoaniline 
• 60490-95-1 (E)-bis-(2,4,6-tribromo-phenyl)-diazene dioxide 

Downstream Products

• 142600-03-1 C₁₁H₉Br₃NO₃ 
• 36622-77-2 C₁₀H₈Br₃N₂O 
• 142617-32-1 C₁₁H₁₀Br₃N₂O 
• 142599-94-8 C₁₂H₁₀Br₃N₂O₃ 
• 168297-38-9 2,4,6-tribromo(tert-butyl-NNO-azoxy)benzene 
• 67384-84-3 methyl-2,4,6-tribromophenylnitroxyl 
• 72588-01-3 2',4',6'-Tribrom-N-(2,7-dimethyl-9-fluorenyliden)anilin 
• 642-95-5 2,3,4-tribromoaniline 
• 1003017-86-4 1,3-bis(2,4,6-trimethylphenyl)-1,3-dihydro-2H-imidazol-2-one 
• 1259282-12-6 C₂₀H₁₀Br₆N₂O₂ 
• 138996-21-1 1-(2,4,6-tribromophenyl)-2-(2-bromo-2-phenylethyl)diazene 1-oxide 
• 76626-01-2 benzyl-2,4,6-tribromophenylnitroxyl 

Relevant academic research and scientific papers

Deoxygenation of nitrosoarene by N-heterocyclic carbene (NHC): an elusive Breslow-type intermediate bridging carbene and nitrene

N-Heterocyclic carbene (NHC) activates and deoxygenates nitrosoarene (ArNO) to afford arylnitrene (ArN), thereby portraying a fundamental route connecting two 6e?species. A combination of spectroscopic and computational studies suggests that th

PRESSURE EFFECT ON DIMERIZATION EQUILIBRIA OF A SERIES OF SUBSTITUTED NITROSOBENZENES IN SOLUTION.

The effect of pressure was studied on the dimerization reactions of six di- and tri-substituted nitrosobenzenes in carbon tetrachloride at 25 degree C. The obtained configurational volume changes for the prototype one bond formation reactions are in the range of minus 17 to minus 21 cm**3 mol** minus **1 at 6. 13 MPa. The volume changes were interpreted in terms of the perturbation theory of liquid; they were dominated by the volume change in the reference system composed of hard spheres. Small differences between the observed and theoretical reference volume changes were ascribed to the perturbation due to electrostatic interactions between the solute and solvent; the perturbation volume changes were estimated by the Kirkwood theory of dipolar solvation.