69448-36-8

Upstream product

• 20115-81-5 1,2-bis(o-hydroxyphenoxy)ethane 
• 79-08-3 bromoacetic acid 
• 105-36-2 ethyl bromoacetate 
• 73961-19-0 2,2'-(Ethylendioxy)diphenoldibenzylether 

Downstream Products

• 211870-42-7 1,2-bis<2-(2-methylsulfonyloxyethyloxy)phenoxy>ethane 
• 68380-65-4 1,2-bis(2-ethoxyphenol)ethane 

Relevant academic research and scientific papers

Novel Dibenzopolyether Resin Possessing Dicarboxylic Acid Side Arm Fuctionality for Use in Specific Lead(II) Separation

A novel dibenzopolyether resin possessing dicarboxylic acid side arm functionality (EDPAR) was synthesized by condensation polymerization of ethylenedi(oxy-o-phenoxyacetic acid) with formaldehyde in formic acid.The exellent sorption for Pb(II) over Cu(II)

Calix[4]arene dibenzocrown ethers as caesium selective extractants

A series of 1,3-dialkyloxycalix[4]arene dibenzocrown ethers were synthesized in the fixed 1,3-alternate conformation with good yields by the reaction of 1,3-dialkyloxycalix[4]arenes with dibenzodimesylate in the presence of caesium carbonate. The three dimensional 1,3-alternate conformation was confirmed by X-ray crystal structure. Upon two phase extraction, NMR studies on the ligand-metal complex, single ion and competitive ion transport experiments through a bulk liquid membrane, 1,3-dipropyloxycalix[4]arene dibenzocrown-6, in which two benzo groups are symmetrically attached to the crown-6 linkage, gave one of the most efficient and selective extractabilities for caesium ion over other alkali metal ions. From supported liquid membrane experiments using 1 and 3 as organic carriers, permeation coefficients of the caesium ion were estimated to be 0.42 and 0.27 cm h-1, respectively. The selectivity of caesium over sodium ion was observed to increase with permeation time.

Studies on complexation of alkaline earth metal cations with acyclic polyether dicarboxylic acids

Acyclic polyether dicarboxylic acids having butyl and tetradecyl side alkyl chains at the α-position of the carboxylic acid sidearm unit were prepared by the reaction of bisphenol and 2-bromoalkanoic acid in the presence of sodium hydride with quantitativ

Calcium ionophores as cardiac stimulants. I. Diacids derived from dibenzo crown ethers

A series of calcium chelating agents has been prepared based on carboxylic derivatives of open chain 18-Crown-6 analogues. Most of these are efficient calcium binding agents, many form lipophilic calcium complexes, and some of these are capable of releasing Ca2+ from liposomes by ionophore action. The best of these is 1,2-bis-[2-(1-carboxydecyloxy)phenoxy]ethane. This compound is cardiotonic in vitro but in the dog vasoconstriction it is the predominant biological effect.