61613-22-7

Basic information

• Product Name: 2-Bromodiphenylamine
• Synonyms: 2-Bromodiphenylamine;2-BDPA;2-bromo-n-phenylaniline;2-bromo-N-phenylbenzenamine;Benzenamine, 2-bromo-N-phenyl-
• CAS NO: 61613-22-7
• Molecular Formula: C₁₂H₁₀BrN
• Molecular Weight: 248.1185
• Mol File: 61613-22-7.mol
• Article Data: 46

Chemical Properties

• Melting Point: 49 °C
• Boiling Point: 323.2±25.0 °C(Predicted)
• Appearance: /
• Density: 1.445±0.06 g/cm3(Predicted)
• Refractive Index: 1.66
• Storage Temp.: Keep in dark place,Inert atmosphere,Room temperature
• PKA: -1.00±0.20(Predicted)
• CAS DataBase Reference: 2-Bromodiphenylamine(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Bromodiphenylamine(61613-22-7)
• EPA Substance Registry System: 2-Bromodiphenylamine(61613-22-7)

Safety Data

• Hazardous Substances Data: 61613-22-7(Hazardous Substances Data)

Usage

General Description

2-Bromodiphenylamine is a chemical compound used primarily in the pharmaceutical and chemical industries. It functions as an important intermediate in the production of a variety of pharmaceutical drugs and fine chemicals. The compound has the molecular formula C12H10BrN and is known for its high reactivity. Handling and usage of this chemical require appropriate safety measures due to its potentially harmful effects on human health and the environment. It is not naturally occurring and is usually produced through the bromination of diphenylamine. Its properties and exact uses can depend on the grade of purity.

Upstream product

• 108-86-1 bromobenzene 
• 615-36-1 2-bromoaniline 
• 622-37-7 Phenyl azide 
• 602-56-2 9-phenylacridine 
• 62-53-3 aniline 
• 122-39-4 diphenylamine 
• 98-95-3 nitrobenzene 
• 244205-40-1 (2-bromophenyl)boronic acid 
• 577-19-5 2-nitrophenyl bromide 
• 98-80-6 phenylboronic acid 
• 19519-75-6 1-bromo-2-nitrosobenzene 
• 586-96-9 Nitrosobenzene 
• 88284-48-4 2-(trimethylsilyl)phenyl trifluoromethanesulfonate 
• 583-55-1 1-Bromo-2-iodobenzene 

Downstream Products

• 1507400-93-2 N-(2-bromophenyl)-N-phenylcyanamide 
• 1290129-46-2 N-2-bromophenyl-N-phenylaminomethane 
• 1484-12-4 N-methylcarbazole 
• 1592-95-6 3-bromo-9H-carbazole 
• 99941-46-5 9-methyl-9-phenyl-10-methyl-9,10-dihydroacridine 
• 87043-43-4 9-ethyl-9-phenyl-10-methyl-9,10-dihydroacridine 
• 1290129-51-9 1,1,1,3,3,3-hexafluoro-2-(2-(methyl(phenyl)amino)phenyl)propan-2-ol 
• 1290129-48-4 9-isopropyl-9,10-dimethyl-9,10-dihydroacridine 

Relevant articles and documents

Highly efficient blue organic light-emitting diodes from pyrimidine-based thermally activated delayed fluorescence emitters

Three highly efficient blue thermally activated delayed fluorescence (TADF) emitters, 2SPAc-HPM, 2SPAc-MPM and 2SPAc-PPM, have been synthesised based on pyrimidine (PM), 2-methylpyrimidine (MPM) and 2-phenylpyrimidine (PPM) as the acceptor and 10H-spiro[acridan-9,9′-fluorene] (2SPAc) as the donor moiety. With their appropriate molecular design, these emitters successfully achieve small singlet-triplet splitting energies for efficient reverse intersystem crossing, and exhibit high photoluminescence quantum yields. As a result, TADF OLEDs based on 2SPAc-HPM, 2SPAc-MPM and 2SPAc-PPM emit blue light peaking at 479-489 nm and generate very high external quantum efficiencies of 25.56%, 24.34% and 31.45%, respectively. The 2SPAc-PPM-based TADF OLED is also one of the very few blue TADF emitters with an external quantum efficiency of more than 30%, and it has the best OLED performance among the pyrimidine-based TADF emitters.

HETEROCYCLIC COMPOUND AND ORGANIC LIGHT EMITTING DEVICE COMPRISING THE SAME

The present specification relates to a heterocyclic compound of Formula 1 and an organic light emitting device including the same.

Chitosan nanoparticles functionalized poly-2-hydroxyaniline supported CuO nanoparticles: An efficient heterogeneous and recyclable nanocatalyst for N-arylation of amines with phenylboronic acid at ambient temperature

The present study aims to prepare an effective and eco-friendly nanocatalyst for the Chan–Lam coupling reaction of phenylboronic acid and amine in aerobic conditions. For this purpose, chitosan was extracted from shrimp shells waste by demineralization, deproteinization, and deacetylation processes and then converted to chitosan nanoparticles (CSN) by the ionic gelation with tripolyphosphate anions. Afterward, poly-2-hydroxyaniline (P2-HA) was grafted to chitosan nanoparticles (NPs) to employ as the support for CuO NPs. Characterization of the nanocatalyst was done using Fourier transform infrared (FT-IR), X-ray powder diffraction (XRD), scanning electron microscopy (SEM), mapping, energy-dispersive X-ray spectroscopy (EDS), transmission electron microscopy (TEM), and thermogravimetric analysis (TGA). The CuO NPs were identified in the spherical shape with an average size of 17 nm. The prepared nanocatalyst exhibited excellent catalytic performance with a high turnover number (TON) and turnover frequency (TOF) for the Chan–Lam coupling reaction of phenyl boronic acid and amines with different electronic properties. The prepared catalyst could be readily recovered and reused for at least five runs without any noticeable change in structure and catalytic performance. Chitosan (CS) was prepared via demineralization, deproteinization, and deacetylation of shrimp shell and chitosan nanoparticles (CSN) were prepared via ionic gelation process. Polymerization of 2-HA on the CSN surface was done to increase functional groups and create active sites for CuO NPs attachments. CuO NPs-P2-HA-CSN nanocomposite has been shown high efficiently for the Chan–Lam coupling reaction.