123824-57-7

Basic information

• Product Name: 1-bromo-9-phenyl-3,6,9-trioxanonane
• Synonyms: 1-bromo-9-phenyl-3,6,9-trioxanonane
• CAS NO: 123824-57-7
• Molecular Weight: 289.169
• Mol File: 123824-57-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1-bromo-9-phenyl-3,6,9-trioxanonane(CAS DataBase Reference)
• NIST Chemistry Reference: 1-bromo-9-phenyl-3,6,9-trioxanonane(123824-57-7)
• EPA Substance Registry System: 1-bromo-9-phenyl-3,6,9-trioxanonane(123824-57-7)

Safety Data

• Hazardous Substances Data: 123824-57-7(Hazardous Substances Data)

Upstream product

• 104-68-7 2-(2-phenoxyethoxy)ethanol 
• 123824-56-6 1-bromo-6-phenyl-3,6-dioxahexane 
• 7204-16-2 2-(2-(2-phenoxyethoxy)ethoxy)ethan-1-ol 

Downstream Products

• 333382-87-9 2-(2-(2-(2-(4-bromophenoxy)ethoxy)ethoxy)ethoxy)ethan-1-ol 
• 125808-05-1 1-bromo-4-(2-(2-(2-methoxyethoxy)ethoxy)ethoxy)benzene 
• 36366-93-5 2-<2-<2-(2-phenoxyethoxy)ethoxy>ethoxy>ethanol 
• 80392-33-2 1-(2-(2-(2-methoxyethoxy)ethoxy)ethoxy)benzene 

Relevant articles and documents

SELECTIV BROMINATION OF THE AROMATIC RING IN ω-PHENYLPOLYOXAALKANES AND ALKANOLS IN MICELLES

The regioselecticity of bromination of ω-phenylpolyoxaalkanes and alkanols by bromine in aqueous solution of dodecyl sulfate (SDS) and aqueous solution of cetyltrimethylammonium bromide (CTAB) are shown to be related to the average orientation of substrate as indicated by 1H NMR studies.Thus ortho-bromination is promoted at higher concentrations of the surfactant relative to pure water.In contrast, at an equal ratio of the surfactant and substrate para-bromination is promoted.The results are discussed with respect to the average orientation of substrate in a micellar microenvironment and the formation of an ether-bromine comples as possible bromination agent.