16292-17-4

Basic information

• Product Name: BIS(4-BROMOPHENYL)AMINE
• Synonyms: 4,4'-DIBROMODIPHENYLAMINE;BIS(4-BROMOPHENYL)AMINE;4,4μ-Dibromodiphenylamine, N-phenyl-4,4μ-dibromoaniline;N-phenyl-4,4μ-dibromoaniline;Bis(4-bromophenyl)amine,4,4′-Dibromodiphenylamine, N-phenyl-4,4′-dibromoaniline;BenzenaMine,4-broMo-N-(4-broMophenyl)-;Double(4-BroMophenyl)aMine;Bis(p-bromophenyl)amine
• CAS NO: 16292-17-4
• Molecular Formula: C₁₂H₉Br₂N
• Molecular Weight: 327.01
• EINECS: 1312995-182-4
• Mol File: 16292-17-4.mol
• Article Data: 49

Chemical Properties

• Melting Point: 106 °C
• Boiling Point: 380.5 °C at 760 mmHg
• Flash Point: 183.9 °C
• Appearance: /
• Density: 1.74 g/cm³
• Vapor Pressure: 5.42E-06mmHg at 25°C
• Refractive Index: 1.68
• Storage Temp.: Keep in dark place,Inert atmosphere,Room temperature
• Solubility: soluble in Methanol
• PKA: -0.55±0.40(Predicted)
• CAS DataBase Reference: BIS(4-BROMOPHENYL)AMINE(CAS DataBase Reference)
• NIST Chemistry Reference: BIS(4-BROMOPHENYL)AMINE(16292-17-4)
• EPA Substance Registry System: BIS(4-BROMOPHENYL)AMINE(16292-17-4)

Safety Data

• Hazard Codes: Xn
• Statements: 22-41
• Safety Statements: 26-36/39
• WGK Germany: 3
• Hazardous Substances Data: 16292-17-4(Hazardous Substances Data)

Usage

Chemical Properties

Off-white powder

InChI:InChI=1/C12H9Br2N/c13-9-1-5-11(6-2-9)15-12-7-3-10(14)4-8-12/h1-8,15H

Upstream product

• 122-39-4 diphenylamine 
• 5149-12-2 4,4'-dibromodiphenylnitrosamine 
• 589-87-7 1,4-bromoiodobenzene 
• 589-21-9 (4-bromophenyl)hydrazine 
• 65178-51-0 N-allyldiphenylamine 
• 106-95-6 allyl bromide 
• 583-55-1 1-Bromo-2-iodobenzene 
• 615-36-1 2-bromoaniline 
• 5467-74-3 4-Bromophenylboronic acid 
• 106-40-1 4-bromo-aniline 
• 673-40-5 4-bromobenzenediazonium tetrafluoroborate 
• 5149-08-6 1,1-bis(4-bromophenyl)hydrazine 
• 621-23-8 1,2,3-trimethoxybenzene 
• 4051-56-3 N,N-diphenylbenzamide 

Downstream Products

• 99234-92-1 N,N-bis-(4-bromophenyl)benzamide 
• 55245-35-7 N,N-bis(4-bromophenyl)carbamoyl chloride 
• 197144-27-7 4,4’-dibromo-N-(tert-butoxycarbonyl)phenylaniline 
• 144393-34-0 4-bromo-N-(4-bromophenyl)-N-(4-nitrophenyl)amine 
• 1322090-89-0 bis[(biphenyl-1',2',3',5',6'-d5)-4-yl]amine 
• 1322090-90-3 4,4'-bis{bis[(biphenyl-1',2',3',5',6'-d5)-4-yl]amino}biphenyl 
• 102113-98-4 bis(biphenyl-4-yl)amine 
• 100308-69-8 4,4′-dibromo-4′′-methoxytriphenylamine 
• 1581259-05-3 ethyl 2-[N,N-bis(4-bromophenyl)sulfamoyl]-2-diazoacetate 
• 1581258-82-3 ethyl 5-bromo-1-(4-bromophenyl)-1,3-dihydrobenzo[c]isothiazole-3-carboxylate 2,2-dioxide 
• 1581259-52-0 ethyl 2-[N,N-bis(4-bromophenyl)sulfamoyl]acetate 
• 25069-38-9 N,N-bis(4-bromophenyl)aminobenzaldehyde 
• 113664-28-1 4-cyano-4′,4′′-dibromotriphenylamine 

Relevant articles and documents

Perovskite Solar Cells Based on Oligotriarylamine Hexaarylbenzene as Hole-Transporting Materials

A cobalt-catalyzed cyclotrimerization of bis(aryl)alkyne is used as an innovative tool to obtain hole-transport materials (HTMs). The novel HTM containing six units of oligotriarylamine (HAB1), characterized by UV-vis, cyclic voltammetry, DFT, and thermogravimetric analysis, confirms its suitability as an efficient HTM in PSCs. A PCE of 17.5% was obtained in HAB1-containing PSCs, a performance comparable to that obtained with spiro-OMeTAD and with slightly better thermal stability.

DMSO-allyl bromide: A mild and efficient reagent for atom economic one-pot: N -allylation and bromination of 2°-aryl amines, 2-aryl aminoamides, indoles and 7-aza indoles

A mixture DMSO-allyl bromide has been developed as a reagent for an atom economic one-pot N-allylation and aryl bromination under basic conditions. Utilizing this reagent, N-allylation-bromination of a number of 2°-aryl amines, aryl aminoamides, indoles, and 7-aza indoles has been achieved. The scope of the substrates and limitations, the synthetic utility of the products, and a plausible reaction mechanism have been proposed.

High-Throughput Mass Spectrometry Screening Platform for Discovering New Chemical Reactions under Uncatalyzed, Solvent-Free Experimental Conditions

A gas-phase high-throughput reaction screening platform was developed for the first time to study chemical structures of closely related functional groups and for the discovery of novel organic reaction pathways. Experiments were performed using the contained atmospheric pressure chemical ionization (APCI) source that enabled nonthermal, nonequilibrium plasma chemistry to be monitored by mass spectrometry (MS) in real time. This contained-APCI MS platform allowed an array of reagents to be tested, resulting in the studies of multiple gas-phase reactions in parallel. By exposing headspace vapor of the selected reagents to corona discharge, solvent-free Borsche-Drecsel cyclization reaction, Katritzky chemistry, and Paal-Knorr pyrrole synthesis were examined in the gas phase, outside the high vacuum environment of the mass spectrometer. A new radical-mediated hydrazine coupling reaction was also discovered, which provided a selective pathway to synthesize secondary amines without using a catalyst. The mechanisms of these atmospheric pressure gas-phase reactions were explored through the direct capture of intermediates and via comparison with the corresponding bulk solution and droplet-phase reactions.