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Bromo[bis(pentafluorophenyl)]thallane

Base Information Edit
  • Chemical Name:Bromo[bis(pentafluorophenyl)]thallane
  • CAS No.:1735-62-2
  • Molecular Formula:C12BrF10Tl
  • Molecular Weight:618.403
  • Hs Code.:
  • DSSTox Substance ID:DTXSID30499408
  • Mol file:1735-62-2.mol
Bromo[bis(pentafluorophenyl)]thallane

Synonyms:Bromo[bis(pentafluorophenyl)]thallane;1735-62-2;DTXSID30499408;bis(pentafluorophenyl) thallium(iii) bromide

Suppliers and Price of Bromo[bis(pentafluorophenyl)]thallane
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
Total 0 raw suppliers
Chemical Property of Bromo[bis(pentafluorophenyl)]thallane Edit
Chemical Property:
  • PSA:0.00000 
  • LogP:2.34680 
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:10
  • Rotatable Bond Count:2
  • Exact Mass:617.87680
  • Heavy Atom Count:24
  • Complexity:376
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1(=C(C(=C(C(=C1F)F)[Tl](C2=C(C(=C(C(=C2F)F)F)F)F)Br)F)F)F
Technology Process of Bromo[bis(pentafluorophenyl)]thallane

There total 2 articles about Bromo[bis(pentafluorophenyl)]thallane 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:
In toluene; addition of C6F5MgBr (in ether) to a solution of TlCl3 in boiling toluene;;
Guidance literature:
In diethyl ether; addition of TlCl3 to C6F5MgBr (molar ratio 3 : 8), 1.5 hours;;
Guidance literature:
In benzene; stirring for 5 h at 20°C;
DOI:10.1016/S0022-328X(00)84425-3
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