1438900-61-8

Basic information

• Product Name: N⁴,N⁴,N^4',N^4'-tetrabenzyl-2,2'-dichloro-[1,1'-biphenyl]-4,4'-diamine
• Synonyms: N⁴,N⁴,N^4',N^4'-tetrabenzyl-2,2'-dichloro-[1,1'-biphenyl]-4,4'-diamine
• CAS NO: 1438900-61-8
• Molecular Weight: 613.629
• Mol File: 1438900-61-8.mol

Chemical Properties

• CAS DataBase Reference: N⁴,N⁴,N^4',N^4'-tetrabenzyl-2,2'-dichloro-[1,1'-biphenyl]-4,4'-diamine(CAS DataBase Reference)
• NIST Chemistry Reference: N⁴,N⁴,N^4',N^4'-tetrabenzyl-2,2'-dichloro-[1,1'-biphenyl]-4,4'-diamine(1438900-61-8)
• EPA Substance Registry System: N⁴,N⁴,N^4',N^4'-tetrabenzyl-2,2'-dichloro-[1,1'-biphenyl]-4,4'-diamine(1438900-61-8)

Safety Data

• Hazardous Substances Data: 1438900-61-8(Hazardous Substances Data)

Upstream product

• 89170-76-3 N,N-dibenzyl-3-chlorobenzenamine 

Relevant articles and documents

Electrochemical synthesis of symmetrical benzidines through dehydrogenative cross-coupling reaction

Synthesis of diversely functionalized symmetrical benzidines through electrochemical dehydrogenative cross-coupling reaction of two N,N-disubstituted anilines, is described. The reactions conducted under mild conditions with no oxidizing reagents and transition metal catalysts.

Synthesis of benzidine derivatives via FeCl3·6H 2O-promoted oxidative coupling of anilines

Under open-flask conditions in the presence of commercially available FeCl3·6H2O, N,N-disubstituted anilines can be converted into diversely functionalized benzidines with yields of up to 99%. Oxidative coupling was extended to N-monosubstituted anilines, and the method was applied to the efficient preparation of 6,6′-biquinoline. Mechanistic investigations have also been performed to explain the observed reactivities.