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9,9'-Diphenyl-9H,9'H-3,3'-bicarbazole

Base Information Edit
  • Chemical Name:9,9'-Diphenyl-9H,9'H-3,3'-bicarbazole
  • CAS No.:57102-62-2
  • Molecular Formula:C36H24N2
  • Molecular Weight:484.6
  • Hs Code.:
  • Mol file:57102-62-2.mol
9,9'-Diphenyl-9H,9'H-3,3'-bicarbazole

Synonyms:

Suppliers and Price of 9,9'-Diphenyl-9H,9'H-3,3'-bicarbazole
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • TCI Chemical
  • 9,9'-Diphenyl-9H,9'H-3,3'-bicarbazole >98.0%(HPLC)
  • 1g
  • $ 296.00
  • TCI Chemical
  • 9,9'-Diphenyl-9H,9'H-3,3'-bicarbazole >98.0%(HPLC)
  • 5g
  • $ 885.00
  • AK Scientific
  • 9,9'-Diphenyl-9H,9'H-3,3'-bicarbazole
  • 1g
  • $ 465.00
  • Activate Scientific
  • 9,9'-Diphenyl-9H,9'H-3,3'-bicarbazole 98%
  • 1 g
  • $ 224.00
Total 13 raw suppliers
Chemical Property of 9,9'-Diphenyl-9H,9'H-3,3'-bicarbazole Edit
Chemical Property:
  • Melting Point:204.0 to 208.0 °C 
  • Boiling Point:721.9±60.0 °C(Predicted) 
  • Density:1.19±0.1 g/cm3(Predicted) 
Purity/Quality:

97% *data from raw suppliers

9,9'-Diphenyl-9H,9'H-3,3'-bicarbazole >98.0%(HPLC) *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Description 9,9'-Diphenyl-9H,9'H-3,3'-bicarbazole (BCzPh), with two conjugated carbazole units, is an electron-rich host material used for phosphorescent organic light-emitting diodes (PHOLEDs). Being electron-rich, BCzPh is also used as an electron donor to form exciplexes either as an emitting layer or host material for highly-efficient fluorescent and phosphorescent OLED devices.
Technology Process of 9,9'-Diphenyl-9H,9'H-3,3'-bicarbazole

There total 10 articles about 9,9'-Diphenyl-9H,9'H-3,3'-bicarbazole which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
N-phenylcarbazole; With methanesulfonic acid; In dichloromethane; at 0 ℃; Inert atmosphere;
With 2,3-dicyano-5,6-dichloro-p-benzoquinone; In dichloromethane; at 20 ℃; for 0.0166667h; Reagent/catalyst; regioselective reaction; Inert atmosphere;
DOI:10.1021/acs.joc.8b02322
Guidance literature:
bromobenzene; 9-phenyl-3,3'-bicarbazole; With potassium tert-butylate; In toluene; for 0.5h; Inert atmosphere;
With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; XPhos; In toluene; for 7h; Reflux;
Guidance literature:
With tetrakis(triphenylphosphine) palladium(0); potassium carbonate; In tetrahydrofuran; water; at 80 ℃; for 12h; Inert atmosphere;
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