165820-78-0

Basic information

• Product Name: N¹,N³,N⁵-tris(4-tert-butylphenyl)benzene-1,3,5-triamine
• Synonyms: N¹,N³,N⁵-tris(4-tert-butylphenyl)benzene-1,3,5-triamine
• CAS NO: 165820-78-0
• Molecular Weight: 519.773
• Mol File: 165820-78-0.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: N¹,N³,N⁵-tris(4-tert-butylphenyl)benzene-1,3,5-triamine(CAS DataBase Reference)
• NIST Chemistry Reference: N¹,N³,N⁵-tris(4-tert-butylphenyl)benzene-1,3,5-triamine(165820-78-0)
• EPA Substance Registry System: N¹,N³,N⁵-tris(4-tert-butylphenyl)benzene-1,3,5-triamine(165820-78-0)

Safety Data

• Hazardous Substances Data: 165820-78-0(Hazardous Substances Data)

Upstream product

• 108-73-6 3,5-dihydroxyphenol 
• 769-92-6 4-tert-Butylaniline 
• 626-39-1 1,3,5-trisbromobenzene 
• 3972-65-4 1-bromo-4-tert-butylbenzene 
• 638-09-5 benzene-1,3,5-triamine trihydrochloride 

Downstream Products

• 165820-83-7 N¹,N¹,N³,N³,N⁵,N⁵-hexakis(4-(tert-butyl)phenyl)benzene-1,3,5-triamine 

Relevant articles and documents

Helically Twisted Benzene-1,3,5-triamine-fused Porphyrin Dimers

NiII-2,18-dibromo-20-chloroporphyrin was fused with N 1,N 3,N 5-triaryl-1,3,5-benzenetriamine via t-BuONa-promoted one-pot reaction to give a helically twisted nitrogen-doped fused porphyrin dimer with high selectivity instead of a trimeric porphyrin. The dimer shows a red-shifted and broad electronic absorption spectrum and negatively shifted multi-stage oxidation behavior owing to the significant electronic effect of the embedded amine-type nitrogen atoms and inter-porphyrinic interaction. Bis-NiII-dimer was successfully converted to the corresponding bis-ZnII-complex, which exhibits fluorescence at around 650700 nm.

NOVEL 1,3,5-TRIS(ARYLAMINO)BENZENE

The invention provides 1,3,5-tris(arylamino)benzenes represented by the general formula (I) wherein A is naphthyl, anthryl, phenanthryl, biphenylyl or terphenylyl group, and R is alkyl having 1-6 carbon atoms or cycloalkyl group having five or six carbon