4671-23-2

Upstream product

• 831-84-5 1-phenyl-propan-2-one semicarbazone 
• 100-63-0 phenylhydrazine 
• 108-88-3 toluene 
• 103-79-7 1-phenyl-acetone 
• 10147-11-2 propargyl benzene 

Downstream Products

• 4757-69-1 2-methyl-3-phenyl-1H-indole 
• 54124-02-6 5-benzyl-2-phenyl-2H-[1,2,3]diazarsole 
• 85-99-4 2-acetamidobenzophenone 
• 131366-47-7 1-Benzyl-1-phenylazo-aethyl-isocyanat 
• 131366-89-7 1-benzyl-5-methyl-2-phenyl-1,2-dihydro-[1,2,4]triazol-3-one 
• 381730-41-2 5-methyl-3,6-diphenyl-3,6-dihydro-[1,3,4]oxadiazin-2-one 
• 3377-72-8 2-benzylindole 
• 80278-91-7 5-Benzyl-3-(4-methoxy-phenyl)-2-phenyl-2,4-dihydro-[1,2,3]diazaphosphole 3-sulfide 
• 106032-46-6 6-Methyl-5-phenyl-1-phenylamino-2,3-dihydro-1H-pyridin-4-one 
• 131366-36-4 5-Benzyl-5-methyl-2-phenyl-1,2,4-triazolidin-3-one 

Relevant academic research and scientific papers

Zirconium complexes stabilized by amine-bridged bis(phenolato) ligands as precatalysts for intermolecular hydroamination reactions

A series of zirconium complexes bearing amine-bridged bis(phenolato) ligands of different steric and electronic properties have been synthesized, and their activities in catalyzing intermolecular hydroamination reactions have been studied and compared. In

New heterocyclic precursors for thermal generation of reactive, electron-rich 1,2-diaza-1,3-butadienes

Figure presented The preparation and thermolysis of new stable heterocyclic precursors of 1,2-diaza-1,3-butadienes is described. The resulting reactive diazadienes are trapped in situ with N-phenyldiazamaleimide. The effect of precursor structure on the temperature at which the diazadienes are generated is discussed.