479213-74-6

Basic information

• Product Name: 1,3,5-tribromo-2-(allyloxymethyl)-4,6-bis((1S)'-methyl-2'-propenyloxymethyl)-benzene
• Synonyms: 1,3,5-tribromo-2-(allyloxymethyl)-4,6-bis((1S)'-methyl-2'-propenyloxymethyl)-benzene
• CAS NO: 479213-74-6
• Molecular Weight: 553.129
• Mol File: 479213-74-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1,3,5-tribromo-2-(allyloxymethyl)-4,6-bis((1S)'-methyl-2'-propenyloxymethyl)-benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3,5-tribromo-2-(allyloxymethyl)-4,6-bis((1S)'-methyl-2'-propenyloxymethyl)-benzene(479213-74-6)
• EPA Substance Registry System: 1,3,5-tribromo-2-(allyloxymethyl)-4,6-bis((1S)'-methyl-2'-propenyloxymethyl)-benzene(479213-74-6)

Safety Data

• Hazardous Substances Data: 479213-74-6(Hazardous Substances Data)

Upstream product

• 6118-13-4 S-(+)-1-buten-3-ol 
• 479213-71-3 1,3,5-tribromo-2-(allyloxymethyl)-4,6-bis(bromomethyl)benzene 
• 29165-34-2 1,3,5-tris(bromo)-2,4,6-tris(bromomethyl) benzene 
• 608-72-0 2,4,6-tribromomesitylene 

Relevant articles and documents

Intramolecular triple heck reaction. An efficient entry to fused tetracycles with a benzene core

Twelve examples of 1,3,5-tribromo-2,4,6-trienylbenzenes were easily synthesized by alkylation, etherification, and amination methods. Under conditions A and B, a series of tetracycles with a benzene core, i.e., fused 5,6,6-, 6,6,6-, and 6,6,7-tetracyclic compounds, were prepared efficiently via this intramolecular triple Heck reaction protocol.