779-76-0

Upstream product

• 79370-00-6 N,N-bis-(2-chloro-phenyl)-benzamide 
• 615-41-8 2-iodochlorobenzene 
• 95-51-2 o-chloroaniline 
• 694-80-4 2-bromo-1-chlorobenzene 
• 57-13-6 urea 
• 1020-39-9 N-(2-chlorophenyI)benzamide 
• 15999-92-5 (Z)-N-(2-chlorophenyl)benzimidoyl chloride 
• 79369-98-5 N-(2-Chlorphenyl)benzimidsaeure-(2-chlorphenyl)ester 
• 15999-92-5 N-(2-chloro-phenyl)-benzimidoyl chloride 
• 79369-98-5 N-(2-chloro-phenyl)-benzimidic acid-(2-chloro-phenyl ester) 

Downstream Products

• 118508-11-5 Bis(2-chlorphenyl)-trimethylsilyl-amin 
• 79370-05-1 N,N-Bis(2-chlorphenyl)-N',N'-dimethyl-1,3-propandiamin 
• 885-33-6 2-chloro-N-(2-chlorophenyl)-N-methylaniline 
• 1379372-41-4 tris(2-mercaptophenyl)amine 
• 1379372-40-3 tris(2-isopropylthiophenyl)amine 
• 1379372-39-0 bis(2-isopropylthiophenyl)amine 
• 1484-12-4 N-methylcarbazole 

Relevant academic research and scientific papers

COMPOUND FOR ORGANIC ELECTRONIC ELEMENT, ORGANIC ELECTRONIC ELEMENT COMPRISING THE SAME, AND ELECTRONIC DEVICE THEREOF

With a compound represented by formula 1, electrode number 1, number 2 and number 1 and number 2 electrode including a solvent for organic electroluminescence device including electronic device element and which is disclosure, a compound represented by formula 1 organic layer, organic of the electrical component to a predetermined driving voltage, luminous efficiency can be on the organic layer. (by machine translation)

Development of a catalytic electron transfer system mediated by transition metal ate complexes: Applicability and tunability of electron-releasing potential for organic transformations

We have developed a catalytic electron transfer (ET) system composed of a transition metal ate complex (Me3M(II)Li; M = Co(II), Mn(II), Fe(II)) and magnesium. This system (catalytic Me3M(II)Li/Mg) turned out to be effective for various ET reactions, such as the desulfonylation of N-phenylsulfonyl amides, and others (the chemoselective cleavage of O-allyl groups, the reduction of nitro groups, the partial reduction of diketones, and the reductive coupling of diphenyliodonium salt). The ET ability of this system can be tuned by changing the ligands of the ate complexes. This tunability was experimentally and electrochemically demonstrated: alkoxy-ligated and dianion-type ET ate complexes showed attenuated and enhanced reducing abilities, respectively. The modification of the ET abilities was evaluated by means of electrochemical measurements and chemical reactions. These results provide a basis for the design of various tailor-made ET ate complexes.

Variation of xantphos-based ligands in the palladium-catalyzed reaction of aryl halides with ureas

A series of Xantphos-based ligands containing various substituents in the diphenylphosphino groups were synthesized, and their effect on the product yield and ratio in the palladium-catalyzed arylation of ureas with nonactivated aryl halides was studied. The arylation of urea and phenylurea in the presence of Pd2(dba)3-CHCl3, 3,5-(CF3) 2Xantphos, and Cs2CO3 in dioxane at 100°C gave the corresponding N,N′-diarylureas in 62-98% yield.