73728-29-7

Upstream product

• 106-37-6 1.4-dibromobenzene 

Downstream Products

• 34650-00-5 para-⁽³⁾H-anisole 
• 81617-36-9 ortho-⁽³⁾H-anisole 
• 81617-35-8 meta-⁽³⁾H-anisole 
• 3042-22-6 2-phenyl-1H-pyrrole 
• 5145-65-3 N-benzoylpyrrole 
• 7697-46-3 phenyl(1H-pyrrol-2-yl)methanone 
• 27649-43-0 3-phenyl-1H-pyrrole 
• 7126-41-2 3-benzoylpyrrole 
• 635-90-5 1-phenylpyrrole 
• 92-52-4 biphenyl 

Relevant academic research and scientific papers

Investigation of Ion-Molecular Reactions of Nucleogenic Phenyl Cations with 1,4-Diazine Derivatives

The use of nuclear-chemical synthesis, based on the generation of free nucleogenic phenyl cations, allowed for the direct phenylation of the nitrogen atom in 1,4-diazines. The presence of two methyl substituents in the quinoxaline substrate leads to a mar

Preparation of N-phenyl-substituted quinolinium derivatives labeled with tritium by chemonuclear synthesis

A chemonuclear method of synthesis is proposed for obtaining difficultly available phenyl-substituted derivatives of quinoline labeled with tritium. The ion-molecule reaction of free phenyl cations, generated on β-decay of tritium, with the nucleophilic c

Preparation of n-phenylbenzo[h]quinolinium derivatives labeled with tritium

The possibility of a direct phenylation of benzoquinoline nitrogen atom with nucleogenic phenyl cations has been demonstrated. A simple method has been developed for obtaining previously unknown tritium labeled N-phenyl derivatives of benzo[h]quinolinium, which are promising radioactive markers for studying the biological action mechanisms of medicinal substances containing the benzoquinolinium structure.