148077-54-7

Basic information

• Product Name: 4'-bromo-N,N-di-p-tolyl-[1,1'-biphenyl]-4-amine
• Synonyms: 4'-bromo-N,N-di-p-tolyl-[1,1'-biphenyl]-4-amine
• CAS NO: 148077-54-7
• Molecular Weight: 428.371
• Mol File: 148077-54-7.mol
• Article Data: 10

Chemical Properties

• CAS DataBase Reference: 4'-bromo-N,N-di-p-tolyl-[1,1'-biphenyl]-4-amine(CAS DataBase Reference)
• NIST Chemistry Reference: 4'-bromo-N,N-di-p-tolyl-[1,1'-biphenyl]-4-amine(148077-54-7)
• EPA Substance Registry System: 4'-bromo-N,N-di-p-tolyl-[1,1'-biphenyl]-4-amine(148077-54-7)

Safety Data

• Hazardous Substances Data: 148077-54-7(Hazardous Substances Data)

Upstream product

• 106-38-7 para-bromotoluene 
• 106-49-0 p-toluidine 
• 620-93-9 di-p-tolylamine 
• 105946-82-5 4-bromo-4'-iodobiphenyl 
• 92-86-4 4-(4-bromophenyl)bromobenzene 

Downstream Products

• 1088453-46-6 C₂₆H₂₄BNO₂ 
• 1259883-10-7 C₃₉H₃₀N₂O 
• 1259883-27-6 C₃₉H₃₀N₂S 
• 1259882-91-1 C₄₅H₃₅N₃ 
• 1311407-99-4 4’-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-N,N-di-p-tolyl-[1,1‘-biphenyl]-4-amine 
• 1311408-00-0 4-bromo-N,N-di-p-tolyl-[1,1':4',1-terphenyl]-4-amine 
• 108-88-3 toluene 
• 1622206-15-8 N,N-bis[4'-(N',N'-di-4-tolylamino)biphenyl-4-yl]-3-(1-trimethylsiloxy-1,3,3,3-tetrameth yldisiloxan-1-yl)aniline 

Relevant articles and documents

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Compounds according to Formulas 1-33 may be useful in electronic devices such as light-emitting devices. For example, they may be used as hole-transport materials.

Palladium-catalyzed formation of secondary and tertiary amines from aryl dihalides with air-stable ferrocenyl tri- and diphosphines: Synthesis and X-ray structure of efficient catalysts beyond [PdCl2(DPPF)]

Robust, air-stable tridentate and bidentate ferrocenylphosphines 1,2-bis(diphenylphosphino)-1′-(diisopropylphosphino)-4-tert- butylferrocene, L5, and 1,1′-bis(diisopropylphosphino)-3,3′- bis(tert-butyl)ferrocene, L9, combined with 1 mol% of [PdCl(η3- C3H5)]2 led to two new catalytic systems which allow the coupling of aniline derivatives with mono- and dihaloarenes to form functionalized diarylamines and triarylamines. The excellent selectivity of the reactions avoids the deleterious dehalogenation of the substrates and products. The X-ray structure characterization of the related complex [PdCl 2(L9)] is reported in which ligand L9 in its meso form is significantly distorted.

PHOTOTHERAPY METHODS AND DEVICES COMPRISING EMISSIVE ARYL-HETEROARYL COMPOUNDS

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