299215-69-3

Basic information

• Product Name: (E)-1,2-bis(2-bromo-4,5-dimethoxyphenyl)-N,N-dimethylethenylamine
• Synonyms: (E)-1,2-bis(2-bromo-4,5-dimethoxyphenyl)-N,N-dimethylethenylamine
• CAS NO: 299215-69-3
• Molecular Weight: 501.215
• Mol File: 299215-69-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (E)-1,2-bis(2-bromo-4,5-dimethoxyphenyl)-N,N-dimethylethenylamine(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-1,2-bis(2-bromo-4,5-dimethoxyphenyl)-N,N-dimethylethenylamine(299215-69-3)
• EPA Substance Registry System: (E)-1,2-bis(2-bromo-4,5-dimethoxyphenyl)-N,N-dimethylethenylamine(299215-69-3)

Safety Data

• Hazardous Substances Data: 299215-69-3(Hazardous Substances Data)

Upstream product

• 120-14-9 3,4-dimethoxy-benzaldehyde 
• 54370-00-2 2-bromo-4,5-dimethoxybenzyl alcohol 
• 5392-10-9 2-bromo-4,5-dimethoxybenzaldehyde 
• 53207-00-4 1-bromo-2-(bromomethyl)-4,5-dimethoxybenzene 
• 193557-58-3 2-(2-bromo-4,5-dimethoxyphenyl)-2-(N,N-dimethylamino)acetonitrile 
• 54370-01-3 1-bromo-2-(chloromethyl)-4,5-dimethoxy-benzene 

Downstream Products

• 299216-00-5 4,5-bis(2-bromo-4,5-dimethoxyphenyl)isoxazole 
• 96756-82-0 2-bromo-4,5-dimethoxybenzyl 2-bromo-4,5-dimethoxyphenyl ketone 

Relevant articles and documents

A Convenient Strategy for the Synthesis of 4,5-Bis(o-haloaryl)isoxazoles

A series of new 1,2-bis(o-haloaryl)ethanones is efficiently prepared and applied to the synthesis of 4,5-bis(o-haloaryl)isoxazoles. Isolation of intermediate hydroxyisoxazolines, which are structurally examined, provides a definitive proof for a heterocyclization mechanism based on an amine exchange process. The isolation and X-ray crystallographic studies of significant side products such as benzamides and triarylpropionitriles are also described.