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Benzenamine, 4-chloro-N-(4-chlorophenyl)-N-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

20440-96-4

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20440-96-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 20440-96-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,4,4 and 0 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 20440-96:
(7*2)+(6*0)+(5*4)+(4*4)+(3*0)+(2*9)+(1*6)=74
74 % 10 = 4
So 20440-96-4 is a valid CAS Registry Number.

20440-96-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-chloro-N-(4-chlorophenyl)-N-phenylaniline

1.2 Other means of identification

Product number -
Other names 4.4'-Dichlor-TPA

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:20440-96-4 SDS

20440-96-4Relevant academic research and scientific papers

Halogen-substituted triphenylamine derivatives with intense mechanoluminescence properties

Tu, Jin,Fan, Yunhao,Wang, Jiaqiang,Li, Xiaoyu,Liu, Fan,Han, Mengmeng,Wang, Can,Li, Qianqian,Li, Zhen

, p. 12256 - 12262 (2019)

Three triphenylamine (TPA) derivatives, constructed by the introduction of halogen atoms in TPA, show strong mechanoluminescence emissions, partially due to their various electronic configurations by virtue of the electron withdrawing ability of halogen atoms. Careful investigation of their single crystals and the density functional theory (DFT) calculations based on the crystal structure demonstrate that the enhanced intermolecular interactions and the twisted molecular structure contribute to their strong ML emission.

Synthesis of Triarylamines via Sequential C-N Bond Formation

Modha, Sachin G.,Popescu, Mihai V.,Greaney, Michael F.

, p. 11933 - 11938 (2017/11/24)

A one-pot domino N-arylation protocol is described using diaryliodonium reagents under copper catalysis. The reaction uses both aryl groups of the diaryliodonium reagent to generate triarylamines starting from simple anilines, representing an atom-economical preparation of an important class of organic material building blocks.

Copper-catalyzed synthesis of triarylamines from aryl halides and arylamines

Qian, Cunwei,Xu, Shaojie,Zong, Qianshou,Fang, Dong

, p. 1881 - 1885 (2012/10/29)

A simple and efficient methodology for the synthesis of triphenylamines has been demonstrated using copper catalyst with a ligand and tripotassium phosphate as the base. The effect of parameters such as catalyst precursors, ligands, bases and solvents were studied and a series of triphenylamines were obtained with moderate to excellent yields in DMF. This reaction displays great functional groups compatibility in the presence of a broad range of functional groups.

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