41817-83-8

Upstream product

• 79-24-3 Nitroethane 
• 1664-40-0 N-(2-aminoethyl)benzeneamine 
• 534-26-9 lysidine 
• 98-80-6 phenylboronic acid 

Downstream Products

• 122884-19-9 2-(4-Hydroxyphenacyliden)-1-phenylimidazolidin 
• 122884-14-4 1-Phenyl-2-[1-phenyl-imidazolidin-(2E)-ylidene]-ethanone 
• 122884-17-7 1-(2-Chloro-phenyl)-2-[1-phenyl-imidazolidin-(2E)-ylidene]-ethanone 
• 122884-12-2 1-(4-Chloro-phenyl)-2-[1-phenyl-imidazolidin-(2E)-ylidene]-ethanone 
• 122884-22-4 4-{2-[1-Phenyl-imidazolidin-(2E)-ylidene]-acetyl}-benzonitrile 
• 122884-18-8 1-(4-Nitro-phenyl)-2-[1-phenyl-imidazolidin-(2E)-ylidene]-ethanone 
• 122884-16-6 1-(3-Chloro-phenyl)-2-[1-phenyl-imidazolidin-(2E)-ylidene]-ethanone 
• 122884-20-2 1-(4-tert-Butyl-phenyl)-2-[1-phenyl-imidazolidin-(2E)-ylidene]-ethanone 
• 122884-15-5 1-(4-Methoxy-phenyl)-2-[1-phenyl-imidazolidin-(2E)-ylidene]-ethanone 
• 122884-23-5 1-(3,4-Dichloro-phenyl)-2-[1-phenyl-imidazolidin-(2E)-ylidene]-ethanone 
• 122884-24-6 1-(4-Amino-phenyl)-2-[1-phenyl-imidazolidin-(2E)-ylidene]-ethanone 
• 1848-69-7 1-phenylimidazolidin-2-one 
• 122884-21-3 2-[1-Phenyl-imidazolidin-(2E)-ylidene]-1-pyridin-3-yl-ethanone 

Relevant academic research and scientific papers

Electrophilically activated nitroalkanes in reaction with aliphatic diamines en route to imidazolines

A novel synthetic methodology for the assembly of imidazolines via an unusual reaction between nitroalkanes and aliphatic 1,2-diamines in the presence of phosphorous acid is described. In contrast to the related highly efficient preparation of benzimidazoles from aromatic amines, this process represents a major synthetic challenge and for a long time was elusive. Analysis of the method limitations is provided.

Spherical CuO Nanoparticles as Catalyst for Chan–Lam Cross-Coupling Reaction under Base Free Condition

Abstract: An easy methodology has been developed for the N-arylation of imidazole with arylboronic acid in absence of base and ligand with the aid of as-synthesized CuO nanoparticles. The CuO nanoparticles have been synthesized via precipitation route. The as-synthesized copper oxide nanoparticles are well characterized by various analytical and spectroscopic techniques, such as powder XRD, Raman spectroscopy, TEM and BET surface area analyses. The CuO nanoparticles appear as spherical in shape with a surface area of 15.4?m2/g. The mentioned reaction successfully proceeds at moderate temperature in presence of the as-synthesized nanoparticles. The protocol is applicable to a wide variety of electronically diverse precursor moieties signifying its well applicability.