690666-83-2

Basic information

• Product Name: 1-(2-aminophenyl)-1-(2,4,6-trimethoxyphenyl)ethanol
• CAS NO: 690666-83-2
• Molecular Weight: 303.358
• Mol File: 690666-83-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1-(2-aminophenyl)-1-(2,4,6-trimethoxyphenyl)ethanol(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(2-aminophenyl)-1-(2,4,6-trimethoxyphenyl)ethanol(690666-83-2)
• EPA Substance Registry System: 1-(2-aminophenyl)-1-(2,4,6-trimethoxyphenyl)ethanol(690666-83-2)

Safety Data

• Hazardous Substances Data: 690666-83-2(Hazardous Substances Data)

Upstream product

• 1131-40-4 2-bromo-1,3,5-trimethoxybenzene 
• 551-93-9 2-aminoacetophenone 

Downstream Products

• 690666-85-4 N-{2-[1-(2,4,6-trimethoxyphenyl)ethenyl]phenyl}formamide 
• 690666-66-1 1-isocyano-2-[1-(2,4,6-trimethoxyphenyl)ethenyl]benzene 
• 690666-84-3 1-amino-2-[1-(2,4,6-trimethoxyphenyl)ethenyl]benzene 

Relevant articles and documents

An Efficient Synthesis of 2,4-Disubstituted Quinolines by Electrophile-Mediated Cyclization Reactions of 2-Isocyanostyrene Derivatives

A novel quinoline synthesis starting with 2-isocyanostyrene derivatives is described. The treatment of 2-isocyanostyrene derivatives with aldehydes (or acetone) in the presence of a catalytic amount of diethyl ether-boron trifluoride afforded quinoline derivatives carrying a 1-hydroxyalkyl substituent at the 2-position. The use of acetaldehyde diethyl acetal or phenyloxirane as an electrophile under the same conditions gave the corresponding quinoline derivatives, carrying the 1-ethoxyethyl or 2-hydroxy-2-phenylethyl substituent at the 2-position, respectively. 2-Isocyanostyrene derivatives reacted with N,N-dimethyliminium salts without any catalyst to give 2-(1-dimethylaminoalkyl)quinolines.