165820-83-7

Basic information

• Product Name: N¹,N¹,N³,N³,N⁵,N⁵-hexakis(4-(tert-butyl)phenyl)benzene-1,3,5-triamine
• Synonyms: N¹,N¹,N³,N³,N⁵,N⁵-hexakis(4-(tert-butyl)phenyl)benzene-1,3,5-triamine
• CAS NO: 165820-83-7
• Molecular Weight: 916.389
• Mol File: 165820-83-7.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: N¹,N¹,N³,N³,N⁵,N⁵-hexakis(4-(tert-butyl)phenyl)benzene-1,3,5-triamine(CAS DataBase Reference)
• NIST Chemistry Reference: N¹,N¹,N³,N³,N⁵,N⁵-hexakis(4-(tert-butyl)phenyl)benzene-1,3,5-triamine(165820-83-7)
• EPA Substance Registry System: N¹,N¹,N³,N³,N⁵,N⁵-hexakis(4-(tert-butyl)phenyl)benzene-1,3,5-triamine(165820-83-7)

Safety Data

• Hazardous Substances Data: 165820-83-7(Hazardous Substances Data)

Upstream product

• 626-44-8 1,3,5-Triiodobenzene 
• 4627-22-9 bis(4-tert-butylphenyl)amine 
• 626-39-1 1,3,5-trisbromobenzene 
• 769-92-6 4-tert-Butylaniline 
• 35779-04-5 1-tert-butyl-4-iodobenzene 
• 165820-78-0 N¹,N³,N⁵-tris(4-tert-butylphenyl)benzene-1,3,5-triamine 

Relevant articles and documents

Carbazole-Based DABNA Analogues as Highly Efficient Thermally Activated Delayed Fluorescence Materials for Narrowband Organic Light-Emitting Diodes

Carbazole-based DABNA analogues (CzDABNAs) were synthesized from triarylamine by regioselective one-shot single and double borylation. The reaction proceeded selectively at the ortho position of the carbazolyl group, where the highest occupied molecular o

Syntheses and Redox Properties of Di-, Tri-, Tetra-, and Pentaamines

A series of di-, tri-, tetra-, and pentaamines were synthesized as precursors for corresponding di-, tri-, tetra-, and penta(aminium radical-cations) by the aryl-N bond formation reaction between aryl iodides and in situ prepared copper amide in refluxing pyridine.Cyclic voltammograms of meta-connected derivatives consisted of irreversible waves which imply side reactions in addition to oxidation to aminium radical-cations.

Cation Radicals of 1,3,5-Tris(diarylamino)benzenes

Cyclic voltametry and ESR studies reveal the nature of the cation radicals of some 1,3,5-tris(diarylamino)benzenes.Results show effectively delocalized radical cations with long solution lifetimes in cold media but with much less kinetic stability at ambi