67242-17-5

Usage

Uses

Used in Chemical Industry:
Bis(2-bromophenyl)amine is used as a precursor in the synthesis of dyes and pigments for various applications, including coloring textiles, plastics, and other materials. Its chemical structure allows for the creation of a wide range of colorants with specific properties.
Used in Pharmaceutical Industry:
Although not explicitly mentioned in the provided materials, Bis(2-bromophenyl)amine, due to its chemical properties, could potentially be used in the pharmaceutical industry as an intermediate in the synthesis of certain drugs, given its reactive functional groups that can be further modified in chemical reactions.
Used in Research and Development:
In the field of research and development, Bis(2-bromophenyl)amine may be employed as a compound for studying the properties of brominated aromatic amines and their potential applications in new materials or chemical processes.

Upstream product

• 70787-28-9 N-(2-Bromphenyl)benzimidoylchlorid 
• 615-36-1 2-bromoaniline 
• 122-39-4 diphenylamine 
• 19519-75-6 1-bromo-2-nitrosobenzene 
• 244205-40-1 (2-bromophenyl)boronic acid 
• 583-53-9 2,3-dibromobenzene 
• 70787-29-0 N-(2-bromo-phenyl)-benzimidic acid-(2-bromo-phenyl ester) 
• 70787-29-0 N-(2-Bromphenyl)benzimidsaeure-(2-bromphenyl)ester 
• 70787-27-8 N-(2-bromophenyl)benzamide 
• 583-55-1 1-Bromo-2-iodobenzene 
• 70787-30-3 N,N-bis(2-bromophenyl)benzamide 

Downstream Products

• 62033-91-4 N-ethyl-2,2'-dibromodiphenylamine 
• 67242-18-6 2,2′,2''-tribromotriphenylamine 
• 118508-17-1 N,N-Bis(2-bromphenyl)-N,N'-tetramethylen-1,2-ethandiamin 
• 118508-20-6 N,N-Bis(2-bromphenyl)-N-(1-methylpiperidin-3-yl)methyl-amin 
• 111869-71-7 1-<3-propyl>piperidin 
• 118508-19-3 N,N-Bis(2-bromphenyl)-N,N'-dimethyl-2-methyl-1,3-propandiamin 
• 79370-04-0 N,N-Bis(2-bromphenyl)-N',N'-diethyl-1,3-propandiamin 
• 579-92-0 Vanadox 
• 239137-56-5 2,2'-Dibromo-N-(methylsulfonyl)diphenylamine 
• 579490-49-6 2,2'-bis(diphenylphosphino)diphenylamine 
• 18740-72-2 5-ethyl-10-methyl-10-phenyl-5,10-dihydro-phenazasiline 
• 76-51-7 5-ethyl-5,10-dihydro-10,10-diphenylphenazasiline 
• 24942-19-6 Aza-phospha-triptycen 
• 1427210-31-8 N,N-bis(2-vinylphenyl)methylamine 

Relevant academic research and scientific papers

BN-Embedded Polycyclic Aromatic Hydrocarbon Oligomers: Synthesis, Aromaticity, and Reactivity

BN-embedded oligomers with different pairs of BN units were synthesized by electrophilic borylation. Up to four pairs of BN units were incorporated in the large polycyclic aromatic hydrocarbons (PAHs). Their geometric, photophysical, electrochemical, and

Double CH Activation of a Masked Cationic Bismuth Amide

The transformation of C?H bonds into more reactive C?M bonds amenable to further functionalization is of fundamental importance in synthetic chemistry. We demonstrate here that the transformation of neutral bismuth compounds into their cationic analogues can be used as a strategy to facilitate CH activation reactions. In particular, the double CH activation of bismuth-bound diphenyl amide, (NPh2)?, is reported along with simple one-pot procedures for the functionalization of the activated positions. The organometallic products of the first and second CH activation steps were isolated in high yields. Analysis by NMR spectroscopy, single-crystal X-ray diffraction, and DFT calculations revealed unusual ground-state properties (e.g., ring strain, moderate heteroaromaticity), and provided mechanistic insight into the formation of these compounds.

Preparation method of 10,10 - diphenyl silicon heteroacridine

The invention discloses a preparation method of 10,10 - diphenylsilicon heteroacridine, and belongs to the field of fine chemical engineering. The technical problem to be solved by the invention is that the implementation cost is low. The method has the a

Tellurium(II)/Tellurium(III)-Catalyzed Cross-Dehydrogenative C?N Bond Formation

The TeII/TeIII-catalyzed dehydrogenative C?H phenothiazination of challenging phenols featuring electron-withdrawing substituents under mild aerobic conditions and with high yields is described. These unexpected TeII/Tesu

ORGANIC ELECTROLUMINESCENCE DEVICE AND FUSED POLYCYCLIC COMPOUND FOR ORGANIC ELECTROLUMINESCENCE DEVICE

An organic electroluminescence device of an embodiment includes oppositely disposed first electrode and second electrode, and a plurality of organic layers disposed between the first electrode and the second electrode, wherein at least one from among the organic layers includes a fused polycyclic compound represented by Formula 1 below, thereby showing improved emission efficiency.

Compound, display panel and display device

The present invention provides a compound used as a main material, and a display panel and a display device comprising the same, the compound having an azaspiro silicon ring structure represented by chemical formula 1, wherein A1 and A2 are electron accep

Synthesis of Di(hetero)arylamines from Nitrosoarenes and Boronic Acids: A General, Mild, and Transition-Metal-Free Coupling

The synthesis of di(hetero)arylamines by a transition-metal-free cross-coupling between nitrosoarenes and boronic acids is reported. The procedure is experimentally simple, fast, mild, and scalable and has a wide functional group tolerance, including carbonyls, nitro, halogens, free OH and NH groups. It also permits the synthesis of sterically hindered compounds.

Method for simply and efficiently synthesizing boron-nitrogen heteroaromatic hydrocarbons

The invention provides a method for simply and efficiently synthesizing a class of boron-nitrogen heteroaromatic hydrocarbons, wherein the general formula of the finally synthesized compound is defined in the specification, Ar1 and Ar2 are respectively in

SYNTHESIS OF SUBSTITUTED ACRIDINES

Disclosed is a method of making substituted acridines. The method includes the step of reacting a bis(halophenyl) amine with an alkyne for a time and at a temperature to yield a substituted acridine.

HETEROCYCLIC COMPOUND AND ORGANIC LIGHT-EMITTING DEVICE INCLUDING THE SAME

A heterocyclic compound and an organic light-emitting device including the same are provided. The heterocyclic compound may be represented by Formula 1. The substituents and variables of Formula 1 may be as defined in the present disclosure. The organic light-emitting device including the heterocyclic compound represented by Formula 1 may have a low driving voltage, high current density, and high efficiency.