41757-99-7

Basic information

• Product Name: 1,2-bis[2-(2-hydroxyethoxy)ethoxy]benzene
• Synonyms: 1,2-bis[2-(2-hydroxyethoxy)ethoxy]benzene
• CAS NO: 41757-99-7
• Molecular Weight: 286.325
• Mol File: 41757-99-7.mol
• Article Data: 22

Chemical Properties

• CAS DataBase Reference: 1,2-bis[2-(2-hydroxyethoxy)ethoxy]benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-bis[2-(2-hydroxyethoxy)ethoxy]benzene(41757-99-7)
• EPA Substance Registry System: 1,2-bis[2-(2-hydroxyethoxy)ethoxy]benzene(41757-99-7)

Safety Data

• Hazardous Substances Data: 41757-99-7(Hazardous Substances Data)

Usage

Physical state

Clear, colorless liquid

Odor

Faint

Solubility

Soluble in water and many organic solvents

Uses

a. Solvent in manufacturing of paints, coatings, and inks
b. Cleaning products
c. Industrial fluids
d. Chemical intermediate in production of other compounds

Boiling point

High

Volatility

Low

Safety

May cause skin and eye irritation upon direct contact

Upstream product

• 63175-02-0 C₂₄H₃₈O₈ 
• 120-80-9 benzene-1,2-diol 
• 628-89-7 2-(2-Chloroethoxy)ethanol 
• 75-21-8 oxirane 
• 1243655-69-7 1,2-dibromo-4,5-bis[2'-(2-benzyloxyethoxy)ethoxy]benzene 
• 2563-26-0 4,5-dibromobenzene-1,2-diol 
• 118591-58-5 5-tosyloxy-3-oxapentanol 

Downstream Products

• 351183-42-1 1,2-bis(5-hydroxy-3-oxa-1-pentyloxy)-4-(9-anthrylmethyl)benzene 
• 293762-86-4 1,2-bis[2-(2-hydroxyethoxy)ethoxy]-4-nitrobenzene 
• 848640-74-4 C₅₀H₆₂O₁₄S₄ 
• 848640-72-2 2-(2-{2-[2-(2-{3-[2-(2-{2-[2-(2-hydroxy-ethoxy)-ethoxy]-phenoxy}-ethoxy)-ethylsulfanylmethyl]-benzylsulfanyl}-ethoxy)-ethoxy]-phenoxy}-ethoxy)-ethanol 
• 601491-87-6 1,2-bis-[3,6-dioxa-undec-10-enoxy]benzene 
• 357609-92-8 2-[2-(2-{2-[2-(6-Bromohexyloxy)ethoxy]ethoxy}phenoxy)ethoxy]ethanol 
• 72216-45-6 2,3-benzo-1,4,7,10,13,16,19,22-octaoxa-2-cyclotetraeicosene 
• 41024-87-7 1,2-bis(5-hydroxy-3-oxa-1-pentyloxy)benzene ditosylate 
• 114085-83-5 1,2-bis<2-<2-(cinnamoyl)ethoxy>ethoxy>benzene 
• 14098-44-3 2,3,5,6,8,9,11,12-octahydro-1,4,7,10,13-benzopentaoxacyclopentadecin 
• 87117-64-4 2,2'-<1,2-Phenylenbis(oxy-2,1-ethandiyloxy)bisethanol>-didodecylether 
• 1418017-55-6 1,2-dicyano-4,5-bis[2'-(2''-tosyloxyethoxy)ethoxy]benzene 
• 1418017-52-3 1,2-dicyano-4,5-bis[2′-(2′′-hydroxyethoxy)ethoxy]benzene 
• 161807-05-2 1,2-bis<2'-(2''-hydroxyethoxy)ethoxy>-4,5-dibromobenzene 

Relevant articles and documents

The crown ether size and stereochemistry affect the self-assembly, hydrogelation, and cellular interactions of crown ether/peptide conjugates

The discovery of crown ethers and their unique interactions with ions make them play a key role in supramolecular chemistry. In this study, we have developed a new type of amphiphilic crown ether (DB18C6, DB24C8)-conjugated phenylalanine dipeptides for th

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.

Strong induced-fit binding of viologen and pyridine derivatives in adjustable porphyrin cavities

The synthesis and binding properties of new porphyrin cage compounds consisting of a rigid diphenylglycoluril part, which is connected via flexible bis(ethyleneoxy) spacers to a (metallo)porphyrin "roof", are reported. Binding of viologen guests and pyrid