35648-87-4

Basic information

• Product Name: 1,4-BIS[2-(2-HYDROXYETHOXY)ETHOXY] BENZENE
• Synonyms: 1,4-BIS[2-(2-HYDROXYETHOXY)ETHOXY] BENZENE;2,2'-[1,4-phenylenebis(oxy-2,1-ethanediyloxy)] bis[ethanol];2-[2-[4-[2-(2-hydroxyethoxy)ethoxy]phenoxy]ethoxy]ethanol
• CAS NO: 35648-87-4
• Molecular Formula: C₁₄H₂₂O₆
• Molecular Weight: 286.32
• Mol File: 35648-87-4.mol
• Article Data: 7

Chemical Properties

• Melting Point: 78 °C
• Boiling Point: 454.5±45.0 °C(Predicted)
• Appearance: /
• Density: 1.172±0.06 g/cm3(Predicted)
• PKA: 14.06±0.10(Predicted)
• CAS DataBase Reference: 1,4-BIS[2-(2-HYDROXYETHOXY)ETHOXY] BENZENE(CAS DataBase Reference)
• NIST Chemistry Reference: 1,4-BIS[2-(2-HYDROXYETHOXY)ETHOXY] BENZENE(35648-87-4)
• EPA Substance Registry System: 1,4-BIS[2-(2-HYDROXYETHOXY)ETHOXY] BENZENE(35648-87-4)

Safety Data

• Hazardous Substances Data: 35648-87-4(Hazardous Substances Data)

Usage

Type of compound

Aromatic compound

Structure

Contains benzene and multiple hydroxyethoxy groups

Common uses

Component in the production of polycarbonate and epoxy resins
Manufacturing of coatings, adhesives, and sealants
Production of electrical components and electronic devices
Precursor in the synthesis of pharmaceuticals

Industrial and commercial applications

Plays a critical role due to its unique chemical properties and versatility

Upstream product

• 628-89-7 2-(2-Chloroethoxy)ethanol 
• 123-31-9 hydroquinone 
• 118591-58-5 5-tosyloxy-3-oxapentanol 

Downstream Products

• 135974-68-4 C₃₆H₃₂N₄⁽⁴⁺⁾*C₃₂H₆₂O₆Si₂*4F₆P^(1-) 
• 135974-63-9 1,4-bis<2-<2<oxy>ethoxy>ethoxy>benzene 
• 53914-95-7 bis(p-phenylene)[34]crown-10 
• 135974-61-7 1,4-bis[2-(2-hydroxyethoxy)ethoxy]benzene bis(4-methylbenzenesulfonate) 
• 134881-64-4 1,4-bis<2-<2-<2-<2-(4-benzyloxyphenoxy)ethoxy>ethoxy>ethoxy>ethoxy>benzene 
• 175447-66-2 [2-(2-{4-[2-(2-Carboxymethoxy-ethoxy)-ethoxy]-phenoxy}-ethoxy)-ethoxy]-acetic acid 
• 93179-57-8 p-bis<2-(2'-chloroethoxy)ethoxy>benzene 
• 175732-70-4 [2-(2-{4-[2-(2-Chlorocarbonylmethoxy-ethoxy)-ethoxy]-phenoxy}-ethoxy)-ethoxy]-acetyl chloride 
• 181725-39-3 N-{2-[2-(2-Methoxy-acetylamino)-phenoxy]-phenyl}-2-{2-[2-(4-{2-[2-({2-[2-(2-methoxy-acetylamino)-phenoxy]-phenylcarbamoyl}-methoxy)-ethoxy]-ethoxy}-phenoxy)-ethoxy]-ethoxy}-acetamide 
• 134940-40-2 1,4-Bis<2-<2-<2-<2-(4-hydroxyphenoxy)-ethoxy>ethoxy>ethoxy>ethoxy>benzol 
• 138611-00-4 1,4-bis<2-<2-<2-<2-<<2-<2-<2-<2-(4-benzyloxyphenoxy)ethoxy>ethoxy>ethoxy>ethoxy>phenoxy>ethoxy>ethoxy>ethoxy>ethoxy>benzene 
• 142879-02-5 1,4-bis<2-<2-<2-<2-<<2-(2-hydroxyethoxy)ethoxy>phenoxy>ethoxy>ethoxy>ethoxy>ethoxy>benzene 
• 144654-24-0 1,4-bis<2-<2-(o-formylphenoxy)ethoxy>ethoxy>benzene 
• 123995-68-6 C₂₂H₃₀O₁₀ 

Relevant articles and documents

Systematically Studying the Effect of Fluoride on the Properties of Cyclophanes Bearing Naphthalene Diimide and Dialkoxyaryl Groups

Anion–π interactions between the Lewis basic anion fluoride and π-acidic naphthalene diimide was systematically studied in a series of cyclophanes in which the properties are modulated through the influence of a second, electron-rich aromatic unit. The sy

A new class of flavonoids bearing macrocyclic polyethers by stereoselective photochemical cycloaddition reaction

A new class of flavonoids bearing cyclic polyethers involving a phenyl ring was conveniently provided by the intramolecular photochemical dimerization of 2-chromonecarboxylic esters. Irradiation of 2-chromonecarboxylate with a polyether tethered at both ends promoted intramolecular [2 + 2] cyclobutane formation leading to 14- to 27-membered cyclic polyethers. The efficiency depended on the substituted position of the phenyl ring, with ortho- and meta-substituted derivatives giving cycloadducts in good chemical yields and quantum efficiencies, whereas the para-derivatives were inert toward photolysis. X-ray crystallographic analysis revealed that the stereochemistry of the macrocyclic cycloadducts exhibited C2-symmetry.

A highly selective and sensitive polymer-based fluorescence sensor for Hg2+-ion detection via click reaction

Mercury rising: A Highly Selective and sensitive polymer-based fluorescence sensor synthesized using click reactions affords the most-pronounced fluorescence response to Hg2+ ions.