72659-53-1

Basic information

• Product Name: 1,2-Bis<β,β'-(p-bromophenoxy)ethoxy>ethane
• Synonyms: 1,2-Bis<β,β'-(p-bromophenoxy)ethoxy>ethane
• CAS NO: 72659-53-1
• Molecular Weight: 460.162
• Mol File: 72659-53-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1,2-Bis<β,β'-(p-bromophenoxy)ethoxy>ethane(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-Bis<β,β'-(p-bromophenoxy)ethoxy>ethane(72659-53-1)
• EPA Substance Registry System: 1,2-Bis<β,β'-(p-bromophenoxy)ethoxy>ethane(72659-53-1)

Safety Data

• Hazardous Substances Data: 72659-53-1(Hazardous Substances Data)

Upstream product

• 106-41-2 4-bromo-phenol 
• 112-26-5 1,2-bis(2-chloroethoxy)ethane 
• 19249-03-7 triethylene glycol di-(p-toluenesulfonate) 
• 112-27-6 2,2'-[1,2-ethanediylbis(oxy)]bisethanol 

Downstream Products

• 216307-18-5 1,8-bis{4-[5-(4-aminophenyl)-cyclohepta-1,3,6-trien-1-yl]phenoxy}-3,6-dioxaoctane 
• 216307-22-1 1,8-bis{4-[3-(4-aminophenyl)-cyclohepta-1,4,6-trien-1-yl]phenoxy}-3,6-dioxaoctane 
• 216307-23-2 1,8-bis{4-[3-(4-ethylaminophenyl)-cyclohepta-1,4,6-trien-1-yl]phenoxy}-3,6-dioxaoctane 
• 216307-19-6 1,8-bis{4-[5-(4-ethylaminophenyl)-cyclohepta-1,3,6-trien-1-yl]phenoxy}-3,6-dioxaoctane 
• 72659-57-5 1,2-Bis<β,β'-(p-diphenyphosphinophenoxy)ethoxy>ethane 

Relevant articles and documents

Design and synthesis of polymeric chiral bicyclo[3.3.0] diene as reusable ligand for rhodium-catalyzed asymmetric 1,4-addition

A series of A-B type sterically regular bicyclio[3.3.0] diene-based polymers were designed and synthesized as immobilized chiral diene ligands for asymmetric catalysis. With polymeric diene 6b, good to excellent enantioselectivities can be achieved in Rh-catalyzed asymmetric 1,4-addition of arylboronic acids to α,β-unsaturated ketones. A series of A-B type sterically regular bicyclio[3.3.0] diene-based polymers were designed and synthesized as immobilized chiral diene ligands for asymmetric catalysis. By using polymeric diene, good to excellent enantioselectivities can be achieved in Rh-catalyzed asymmetric 1,4-addition of arylboronic acids to α,β-unsaturated ketones. Copyright

Polyethers. 1. Preparation of ω,ω'-Bis(triphenylphosphine) Polyethers

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