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Azobenzene, 2,2',3,3',5,5',6,6'-octafluoro-4,4'-dinitro-

Base Information Edit
  • Chemical Name:Azobenzene, 2,2',3,3',5,5',6,6'-octafluoro-4,4'-dinitro-
  • CAS No.:74632-45-4
  • Molecular Formula:C12F8N4O4
  • Molecular Weight:416.14
  • Hs Code.:
  • DSSTox Substance ID:DTXSID901038899
  • Mol file:74632-45-4.mol
Azobenzene, 2,2',3,3',5,5',6,6'-octafluoro-4,4'-dinitro-

Synonyms:74632-45-4;Azobenzene, 2,2',3,3',5,5',6,6'-octafluoro-4,4'-dinitro-;DTXSID901038899;Diazene, bis(2,3,5,6-tetrafluoro-4-nitrophenyl)- (9CI)

Suppliers and Price of Azobenzene, 2,2',3,3',5,5',6,6'-octafluoro-4,4'-dinitro-
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
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  • price
Total 0 raw suppliers
Chemical Property of Azobenzene, 2,2',3,3',5,5',6,6'-octafluoro-4,4'-dinitro- Edit
Chemical Property:
  • Vapor Pressure:7.18E-10mmHg at 25°C 
  • Boiling Point:506.2°Cat760mmHg 
  • Flash Point:259.9°C 
  • Density:1.96g/cm3 
  • XLogP3:4.2
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:14
  • Rotatable Bond Count:2
  • Exact Mass:415.97917979
  • Heavy Atom Count:28
  • Complexity:552
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:C1(=C(C(=C(C(=C1F)F)[N+](=O)[O-])F)F)N=NC2=C(C(=C(C(=C2F)F)[N+](=O)[O-])F)F
Technology Process of Azobenzene, 2,2',3,3',5,5',6,6'-octafluoro-4,4'-dinitro-

There total 2 articles about Azobenzene, 2,2',3,3',5,5',6,6'-octafluoro-4,4'-dinitro- 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:
With chlorosulfonic acid; at 60 - 70 ℃; for 0.5h;
Guidance literature:
Multi-step reaction with 2 steps
1: 63 percent / tert-butyl hypochlorite / CCl4 / 3 h / 30 °C
2: 3 percent / 300 h / 20 °C / sealed tube
With tert-butylhypochlorite; In tetrachloromethane;
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