89500-36-7

Basic information

• Product Name: 4-chloro-N-(1-(4-chlorophenyl)ethyl)aniline
• Synonyms: 4-chloro-N-(1-(4-chlorophenyl)ethyl)aniline
• CAS NO: 89500-36-7
• Molecular Weight: 266.17
• Mol File: 89500-36-7.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: 4-chloro-N-(1-(4-chlorophenyl)ethyl)aniline(CAS DataBase Reference)
• NIST Chemistry Reference: 4-chloro-N-(1-(4-chlorophenyl)ethyl)aniline(89500-36-7)
• EPA Substance Registry System: 4-chloro-N-(1-(4-chlorophenyl)ethyl)aniline(89500-36-7)

Safety Data

• Hazardous Substances Data: 89500-36-7(Hazardous Substances Data)

Upstream product

• 3391-10-4 1-(p-chlorophenyl)ethyl alcohol 
• 106-47-8 4-chloro-aniline 
• 99-91-2 para-chloroacetophenone 
• 1073-67-2 4-vinylbenzyl chloride 
• 114200-18-9 1-(p-chlorophenyl)ethyl p-nitrobenzenesulfonate 
• 114200-17-8 1-(p-chlorophenyl)ethyl p-chlorobenzenesulfonate 
• 114200-15-6 1-(p-chlorophenyl)ethyl tosylate 
• 114200-16-7 1-(p-chlorophenyl)ethyl benzenesulfonate 
• 25287-47-2 (E)-4-chloro-N-(1-(4-chlorophenyl)ethylidene)aniline 
• 1184002-62-7 1-amino-1,1-bis(4-chlorophenyl)ethane 
• 80-06-8 chlorfenethol 

Relevant articles and documents

Iodine-mediated 1,2-aryl migration of primary benzhydryl amines

An iodine-mediated 1,2-aryl migration reaction of primary benzhydryl amines under transition metal-free conditions has been achieved. The crude imines generated by this rearrangement reaction can be directly transformed into various aromatic secondary ami

N,N-coordination Rh complex as well as synthesis method and application thereof

The invention belongs to the technical field of synthesis of organic metal compounds and particularly relates to an N,N-coordination Rh complex as well as a synthesis method and an application thereof. Firstly, a ligand is synthesized from methyl 1H-pyrrole-2-carboxylate as an initial raw material and further reacts with Rh(COD)2Cl, and a metal complex with Rh as a central atom is obtained. The synthesis method is simple, the complex as a catalyst can be used for catalyzing a series of reductive amination reactions of derivatives of acetophenone and aniline, and the product yield is good and is 90% or above.

Proton-catalyzed hydroamination and hydroarylation reactions of anilines and alkenes: A dramatic effect of counteranions on reaction efficiency

The anilinium salt, [PhNH3][B(C6F5)4], has been identified as a catalyst for the hydroamination and hydroarylation of several different types of alkenes with anilines. The weakly coordinating counterion of this