726-28-3

Upstream product

• 620-51-9 N,N'-di(3-methylphenyl)thiourea 
• 621-29-4 3-tolyl isocyanate 
• 620-50-8 N,N'-di(m-tolyl)urea 
• 35843-75-5 N-triphenylphosphoranylidene-m-toluidine 
• 75-15-0 carbon disulfide 

Downstream Products

• 344954-40-1 Cp₂Zr(N(t-Bu)C=N(m-Tol)N(m-Tol)) 
• 1261527-56-3 5-methyl-1-m-tolyl-2-(piperidin-1-yl)-1H-benzo[d]imidazole 
• 1352008-26-4 (Z)-3-methyl-N-(1-m-tolyl-1H-benzo[d][1,3]oxazin-2(4H)-ylidene)aniline 
• 1215222-94-8 C₂₃H₁₉N₅O₂ 
• 1215222-95-9 C₂₃H₁₉N₅O₂ 
• 859932-58-4 N-anilino-N',N''-di-m-tolyl-guanidine 

Relevant academic research and scientific papers

Pushing back the limits of hydrosilylation: Unprecedented catalytic reduction of organic ureas to formamidines

Pushing back the limits: A novel catalytic transformation has been designed to prepare formamidine derivatives by reduction of substituted ureas with hydrosilanes. Simple iron catalysts based on commercially available iron salts and phosphine ligands prov

Copper(II) acetate/oxygen-mediated nucleophilic addition and intramolecular C-H activation/C-N or C-C bond formation: One-pot synthesis of benzimidazoles or quinazolines

Diarylcarbodiimides or benzylphenylcarbodiimides are converted to 1,2-disubstituted benzimidazoles or 1,2-disustituted quinazolines via addition/intramolecular C-H bond activation/C-N or C-C bond forming reaction using copper(II) acetate/oxygen [Cu(OAc)2/O2] as the oxidant at 100°C in one-pot cascade procedure. Copyright

O-Iodoxybenzoic acid mediated oxidative desulfurization of 1,3-disubstituted thioureas to carbodiimides

An efficient and mild oxidative desulfurization procedure using o-iodoxybenzoic acid has been developed for the synthesis of carbodiimides starting from easily synthesizable 1,3-disubstituted thioureas.