Welcome to LookChem.com Sign In|Join Free
  • or
Benzenamine, 4-bromo-N-(4-methylphenyl)-N-phenyl-, also known as 4-bromo-N,N-diphenylaniline, is a chemical compound with the molecular formula C19H16BrN. It is a derivative of aniline, featuring a bromine atom and two aromatic rings attached to its nitrogen atom. Benzenamine, 4-bromo-N-(4-methylphenyl)-N-phenylis characterized by its unique structure and versatile reactivity, making it a valuable intermediate in the synthesis of various organic compounds.

183798-74-5

Post Buying Request

183798-74-5 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

183798-74-5 Usage

Uses

Used in Pharmaceutical Synthesis:
Benzenamine, 4-bromo-N-(4-methylphenyl)-N-phenylis used as a key intermediate in the synthesis of various pharmaceuticals. Its unique structure allows for the development of new drugs with potential therapeutic applications, such as anti-inflammatory, analgesic, and antipyretic agents.
Used in Agrochemical Production:
Benzenamine, 4-bromo-N-(4-methylphenyl)-N-phenylis also utilized in the production of agrochemicals, including pesticides and herbicides. Its reactivity and stability make it suitable for the development of effective and environmentally friendly agrochemicals.
Used in Dye and Pigment Manufacturing:
Benzenamine, 4-bromo-N-(4-methylphenyl)-N-phenylis used as a building block in the preparation of dyes and pigments. Its aromatic rings and bromine atom contribute to the color and stability of these compounds, making them suitable for various applications, such as textiles, plastics, and printing inks.
Used in Material Science:
In the field of material science, Benzenamine, 4-bromo-N-(4-methylphenyl)-N-phenylis employed as a reagent in chemical reactions for the production of organic compounds. Its unique structure and reactivity enable the synthesis of new materials with specific properties, such as conductivity, magnetism, or optical activity.
Used in the Preparation of Biologically Active Compounds:
Benzenamine, 4-bromo-N-(4-methylphenyl)-N-phenylis also used as a building block in the preparation of various biologically active compounds and materials. Its versatility allows for the development of new compounds with potential applications in medicine, agriculture, and other fields.

Check Digit Verification of cas no

The CAS Registry Mumber 183798-74-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,3,7,9 and 8 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 183798-74:
(8*1)+(7*8)+(6*3)+(5*7)+(4*9)+(3*8)+(2*7)+(1*4)=195
195 % 10 = 5
So 183798-74-5 is a valid CAS Registry Number.

183798-74-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(4-bromophenyl)-4-methyl-N-phenylaniline

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:183798-74-5 SDS

183798-74-5Relevant academic research and scientific papers

The main body of the triphenylamine constructing macrocyclic and a plurality of lateral branch hole transport material, triphenylamine

-

, (2017/02/28)

The invention provides a hole-transporting material with main body big ring built by triphenylamine and replaced by a plurality of triphenylamine lateral branches. 2-bromine fluorenone is built to triphenylamine monomer containing functional groups capable of reacting with each other, three molecules of monomers are further cyclized, and at least three triphenylamine lateral branch structures are built at the side of the big ring to form electron-rich hole-transporting material containing a plurality of main body big ring and lateral branches built by triphenylamine through simple chemical reaction. The electron-rich formulae a, b and c big ring type triarylamine compounds have approximate three-dimensional spherical structures. The synthetic electron-rich big ring type triarylamine compounds have high glass transition temperature, can form stable and uniform amorphous form film, do not emit fluorescence with the wavelength of more than 420 nanometers and can be used in a photovoltaic conversion device as the hole-transporting material.

Chemically doped and cross-linked hole-transporting materials as an efficient anode buffer layer for polymer solar cells

Sun, Ying,Chien, Shang-Chieh,Yip, Hin-Lap,Zhang, Yong,Chen, Kung-Shih,Zeigler, David F.,Chen, Fang-Chung,Lin, Baoping,Jen, Alex K.-Y.

, p. 5006 - 5015 (2012/04/04)

A series of cross-linkable hole-transporting materials (X-HTMs) consisting of indacenodithiophene, bithiophene, and thiophene units bookended by two triarylamine groups have been designed and synthesized to investigate their suitability as new anode buffe

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 183798-74-5