161807-05-2

Basic information

• Product Name: 1,2-bis<2'-(2''-hydroxyethoxy)ethoxy>-4,5-dibromobenzene
• Synonyms: 1,2-bis<2'-(2''-hydroxyethoxy)ethoxy>-4,5-dibromobenzene
• CAS NO: 161807-05-2
• Molecular Weight: 444.117
• Mol File: 161807-05-2.mol

Chemical Properties

• CAS DataBase Reference: 1,2-bis<2'-(2''-hydroxyethoxy)ethoxy>-4,5-dibromobenzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-bis<2'-(2''-hydroxyethoxy)ethoxy>-4,5-dibromobenzene(161807-05-2)
• EPA Substance Registry System: 1,2-bis<2'-(2''-hydroxyethoxy)ethoxy>-4,5-dibromobenzene(161807-05-2)

Safety Data

• Hazardous Substances Data: 161807-05-2(Hazardous Substances Data)

Upstream product

• 54533-84-5 2-(2-(2-chloroethoxy)ethoxy)tetrahydro-2H-pyran 
• 2563-26-0 4,5-dibromobenzene-1,2-diol 
• 118591-58-5 5-tosyloxy-3-oxapentanol 
• 120-80-9 benzene-1,2-diol 
• 1243655-69-7 1,2-dibromo-4,5-bis[2'-(2-benzyloxyethoxy)ethoxy]benzene 
• 41757-99-7 1,2-bis[2-(2-hydroxyethoxy)ethoxy]benzene 

Downstream Products

• 161807-06-3 1,2-bis<2'-(2''-(p-toluenesulfonyloxy)ethoxy)ethoxy>-4,5-dibromobenzene 
• 300853-67-2 4,5-dibromo-1,2-bis{2'-[2''-(methylsulfonyloxy)ethoxy]ethoxy}benzene 
• 300853-68-3 1,2-(7-benzyl-7-aza-1,4,10,13-tetraoxatridecamethylene)-4,5-dibromobenzene 
• 300853-71-8 1,2-(7-benzyloxycarbonyl-7-aza-1,4,10,13-tetraoxatridecamethylene)-4,5-dibromobenzene 
• 300853-74-1 1,2-(7-benzyloxycarbonyl-7-aza-1,4,10,13-tetraoxatridecamethylene)-4,5-dicyanobenzene 
• 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 

Relevant articles and documents

Synthesis and properties of optically active 6,6′-didodecyl-1,1′-binaphthyl-phthalocyanine linked through crown ether units

A novel optically active 6,6′-didodecyl-1,1′-binaphthyl-metallophthalocyanine linked through crown ether units ((S)-Pc) has been synthesized. A stable monolayer of (S)-Pc that is able to bind metal ions can be formed at the air-water interface. Nonlinear

Synthesis and copper(I)-driven disaggregation of a zinc-complexed phthalocyanine bearing four lateral coordinating rings

A new zinc phthalocyaninate, bearing four flexible phenanthroline- containing 30-membered rings was synthesized by template condensation of a macrocyclic phthalonitrile. The resulting phthalocyanine was an insoluble aggregate. However, in the presence of CuI ions, the formation of a soluble complex was observed. UV/Vis and DOSY NMR spectroscopic studies showed a monomolecular state for this species in solution. 1H-1H ROESY demonstrated that the macrocyclic substituents adopt a folded conformation, giving the complex a globular shape. The folding originates from stacking interactions between the phthalocyanine core and peripheral copper(I)-phenanthroline complexes. Copyright

1,2-Dicyano-4,5-bis[2'-(2"-benzyloxyethoxy)ethoxy]benzene-precursor towards new functionalized phthalocyanines

1,2-Dicyano-4,5-bis[2'-(2"-benzyloxyethoxy)ethoxy]benzene can act as a precursor to new functionalized phthalocyanines with liquid crystal properties.

Synthesis of optically active 1,1′-binaphthyl-phthalocyanines linked via a crown ether unit

Novel optically active metal and metal-free phthalocyanines, substituted with 1,1′-binaphthyl crown ether units, have been synthesized and characterized.

Synthesis and supramolecular chemistry of novel liquid crystalline crown ether-substituted phthalocyanines: Toward molecular wires and molecular ionoelectronics

The synthesis of the metal-free and the dihydroxysilicon derivatives of tetrakis[4′,5′-bis(decoxy)benzo-18-crown-6]phthalocyanine is described. The metal-free phthalocyanine is liquid crystalline and exhibits a crystalline phase to mesophase transition at