38573-62-5

Usage

Uses

Used in Pharmaceutical Synthesis:
2,4-dibromo-N-(2,4-dibromophenyl)aniline is used as a key intermediate in the synthesis of pharmaceuticals for its ability to participate in various chemical reactions, contributing to the development of new drugs with potential therapeutic applications.
Used in Agrochemical Production:
In the agrochemical industry, 2,4-dibromo-N-(2,4-dibromophenyl)aniline is utilized as a precursor in the production of pesticides and other agrochemicals, leveraging its reactivity to create compounds that can protect crops from pests and diseases.
Used in Dye Manufacturing:
2,4-dibromo-N-(2,4-dibromophenyl)aniline is employed as a starting material in the manufacturing of dyes, where its chemical structure allows for the creation of a range of colored compounds used in various industries, including textiles and printing.
Used in Organic Chemistry Research:
As an intermediate in the production of other complex organic compounds, 2,4-dibromo-N-(2,4-dibromophenyl)aniline is also used in organic chemistry research to explore new synthetic pathways and develop novel chemical entities.
Safety Note:
It is crucial to handle 2,4-dibromo-N-(2,4-dibromophenyl)aniline with care due to its toxic nature, which can pose risks to human health and the environment if not managed properly. Appropriate safety measures and disposal methods should be strictly adhered to during its use in any application.

Upstream product

• 64-19-7 acetic acid 
• 64-17-5 ethanol 
• 7726-95-6 bromine 
• 122-39-4 diphenylamine 
• 67-66-3 chloroform 
• 382165-80-2 N-nitrosodiphenylamine 
• 60-29-7 diethyl ether 
• 712-51-6 Diphenylaminoxid-Radikal 
• 7732-18-5 water 
• 4733-19-1 10-hydroxy-5,10-dihydrophenarsazine 5-oxide 
• 578-94-9 adamsite 
• 552-82-9 benzhydrylidene(methyl)amine 

Downstream Products

• 64524-09-0 bis(2,4,6-tribromophenyl)amine 
• 1181972-74-6 bis(2,4-dibromophenyl)(4-nitrophenyl)amine 
• 1181972-62-2 bis(2,4-dibromophenyl)(methoxylmethyl)amine 
• 949586-28-1 C₆H₁₃N(C₆H₃Br)2BC₆H₂(CH(CH₃)2)3 
• 949586-25-8 C₆H₁₃N(C₆H₃Br)2BC₆H₂(CH₃)3 
• 93994-38-8 bis(2,4-dibromophenyl)hexylamine 
• 3666-93-1 N-ethyl-2,2',4,4'-tetrabromodiphenylamine 

Relevant academic research and scientific papers

ORGANIC ELECTROLUMINESCENCE DEVICE AND ORGANIC COMPOUND FOR ORGANIC ELECTROLUMINESCENCE DEVICE

The organic electroluminescent device according to an embodiment 1 is an n-type electrode. The EML includes 2 electrodes and an emitting layer disposed between the (1 and 2) th electrodes, and the EML includes the compound represented by Formula 1, and the EML may exhibit high emission efficiency characteristics and improved lifetime characteristics. Chemical Formula 1. Wherein each substituent in Formula 1 is as defined in the description of the invention.

Silicon Substitution in Oxazine Dyes Yields Near-Infrared Azasiline Fluorophores That Absorb and Emit beyond 700 nm

Exchanging the bridging oxygen atom in rhodamine dyes with a dimethylsilyl group red-shifts their excitation and emission spectra, transforming orange fluorescent rhodamines into far-red Si-rhodamines. To study the effect of this substitution in other dye

PHOSPHORESCENT EMITTERS CONTAINING DIBENZO[1,4]AZABORININE STRUCTURE

PROBLEM TO BE SOLVED: To provide a compound comprising dibenzo[1,4]azaborine useful as emitters in organic light emitting devices. SOLUTION: There is provided a compound comprising dibenzo[1,4]azaborine in a ligand represented by the compounds 1-11 and 1-

ORGANIC ELECTROLUMINESCENCE ELEMENT AND MATERIAL FOR ORGANIC ELECTROLUMINESCENCE ELEMENT

Provided are a novel organic electroluminescent device material and an organic electroluminescent device using the same. The organic electroluminescent device material includes a compound represented by the following formula (1). The organic electrolumine

A facile, regioselective and controllable bromination of aromatic amines using a CuBr2/Oxone system

A combination of cupric bromide and Oxone serves as a facile, mild and effective reagent for the bromination of aromatic amines. Primary, secondary and tertiary aromatic amines are all suitable substrates. The reaction possesses high regioselectivity and functional group tolerance, and mono- and multi-brominated products can be obtained controllably in moderate to excellent yields. The Royal Society of Chemistry 2013.

Halogenation Using Quaternary Ammonium Polyhalides. VI. Bromination of Aromatic Amines by Use of Benzyltrimethylammonium Tribromide

The reaction of aromatic amines with benzyltrimethylammonium tribromide in dichloromethane-methanol containing calcium carbonate powder for 0.5 h at room temperature gave bromo-substituted aromatic amines in good yields.

REGIOSELECTIVE MONOBROMINATION OF AROMATIC AMINES WITH TETRABUTYLAMMONIUM TRIBROMIDE

A simple and efficient method for monobromination of aromatic amines predominantly in the para position is reported.Tetrabutylammonium tribromide is used at 20 deg C and yields of parabromoanilines are higher than 90percent.