81865-10-3

Basic information

• Product Name: 2-(4-aminophenyl)ethyl chloride
• Synonyms: 2-(4-aminophenyl)ethyl chloride
• CAS NO: 81865-10-3
• Molecular Weight: 155.627
• Mol File: 81865-10-3.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 2-(4-aminophenyl)ethyl chloride(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(4-aminophenyl)ethyl chloride(81865-10-3)
• EPA Substance Registry System: 2-(4-aminophenyl)ethyl chloride(81865-10-3)

Safety Data

• Hazardous Substances Data: 81865-10-3(Hazardous Substances Data)

Upstream product

• 64-17-5 ethanol 
• 20264-95-3 2-(4-nitrophenyl)ethyl chloride 
• 32327-70-1 1-chloro-4-(2-chloroethyl)benzene 
• 937-20-2 p-chlorophenacyl chloride 
• 108-90-7 chlorobenzene 
• 622-24-2 2-phenylethyl chloride 

Downstream Products

• 391901-45-4 YM-208876 
• 1245920-69-7 C₁₁H₁₃ClN₂O₄S 
• 501-94-0 p-hydroxyphenethyl alcohol 
• 396124-19-9 N-{4-[2-(5-amino-2-furan-2-yl-pyrazolo[4,3-e][1,2,4]triazolo[1,5-c]pyrimidin-7-yl)-ethyl]-phenyl}-acetamide 
• 52273-67-3 N-[4-(2-chloro-ethyl)-phenyl]-acetamide 
• 396124-50-8 2-[4-(N,N-bis-β-hydroxyetylamino)phenyl]ethyl chloride 
• 28145-35-9 4-(2-chloroethyl)phenol 

Relevant articles and documents

Synthetic method of 2-bromo-4-(2-chloro-ethyl)-aniline

The invention relates to a synthetic method of 2-bromo-4-(2-chloro-ethyl)-aniline and belongs to the field of chemical synthesis. The method comprises the following steps: using chlorobenzene and anhydrous AlCl2 as raw materials, dropwise adding chloroacetyl chloride, using ice water and hydrochloric acid, stirring and reacting, carrying out suction filtration, washing with sodium hydroxide and deionized water, carrying out vacuum suction filtration and collecting chlorobenzene, carrying out rotary evaporation until collecting 4-chloro-benzeneacetyl chloride, heating a 4-chloro-benzeneacetyl chloride solution, hydrazine hydrate and diglycol and carrying out reflux reaction, collecting 1-chloro-4-(2-chloroethyl)benzene and drying under reduced pressure to prepare light yellow powder, carrying out a bromination reaction and dropwise adding a sodium hypochlorite solution and an ammonium sulfite solution, washing and collecting saffron yellow particles so as to prepare 2-bromo-4-(2-chloro-ethyl)-aniline.