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

58047-41-9

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58047-41-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58047-41-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,0,4 and 7 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 58047-41:
(7*5)+(6*8)+(5*0)+(4*4)+(3*7)+(2*4)+(1*1)=129
129 % 10 = 9
So 58047-41-9 is a valid CAS Registry Number.

58047-41-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-chloro-N,N-di-p-tolylaniline

1.2 Other means of identification

Product number -
Other names 4-chloro-4',4''-dimethyltriphenylamine

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:58047-41-9 SDS

58047-41-9Downstream Products

58047-41-9Relevant academic research and scientific papers

Effects of solvent and base on the palladium-catalyzed amination: PdCl 2(Ph3P)2/Ph3P-catalyzed selective arylation of primary anilines with aryl bromides

Cai, Liangzhen,Qian, Xuanying,Song, Wenjing,Liu, Taoping,Tao, Xiaochun,Li, Wanfang,Xie, Xiaomin

, p. 4754 - 4759 (2014/06/24)

A readily accessible catalytic system, PdCl2(Ph 3P)2/Ph3P, was developed for the selective arylation of primary anilines with aryl bromides. The strong influence of solvents and bases on the catalytic activity was observed. In refluxing o-xylene, triphenylphosphine shows high efficiency for Pd-catalyzed intermolecular amination reactions. By changing the bases, mono- and diarylation of primary amines could be selectively achieved in high yields. Moreover, the catalytic system showed good toleration for the steric hindrance of anilines. A series of N,N,N′,N′-tetraaryl-1,1′-biphenyl-4,4′- diamines, important intermediates of OLED hole transport materials, were synthesized facilely via coupling reactions between 4,4′-diaminobiphenyls and aryl bromides.

N-ALKYLATION AND N-ARYLATION OF ANILINES STARTING FROM A MILD N-Mg REAGENT: ITS ACTIVATION CAUSING THE 'N-C' COUPLING TO EXTEND THE UNIFIED STRUCTURE-REACTIVITY RELATIONSHIP

Matsuo, Koji,Shichida, Yoshiaki,Nishida, Hiroshi,Nakata, Satsuki,Okubo, Masao

, p. 9 - 17 (2007/10/02)

New N-alkylation and N-arylation procedures starting from anilinomagnesium (ArNHMgBr) are reported.For N-alkylation with alkyl bromides, addition of hexamethylphosphoramide to an ArNHMgBr solution in tetrahydrofuran (THF) is effective.After heating at 55 deg C, N-monoalkylation product was obtained in 60-90percent yield, slight dialkylation taking place.The combined use of aryliminodimagnesium with α,ω-dibromoalkanes led to N-arylazacycloalkanes.For N-arylation with iodobenzene, replacement of THF with pyridine and additional use of copper(I) iodide are effective.After heating at 115 deg C with iodobenzene, mono- and diarylation products were obtained, the former being predominant.The combined use of ArNHMgBr and N,N,N',N'-tetramethylethylenediamine as the ligand of copper species is effective for elimination of diarylation and other undesired products, and leads to diarylamines in excellent yield.The method is of advantage over the conventional Ullmann and Chapman methods.The polar solvents and copper salt are effective additives for inducing 'inert combinations' of ArNHMgBr or ArN(MgBr)2 with alkyl and aryl halides into N-C coupling, to extend the unified view proposed for the reactivity of magnesium reagents.The difference in the roles of N-Mg and N-Cu species is discussed.

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