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Diboron tetrafluoride

Base Information Edit
  • Chemical Name:Diboron tetrafluoride
  • CAS No.:13965-73-6
  • Molecular Formula:B2F4
  • Molecular Weight:97.6156
  • Hs Code.:
  • DSSTox Substance ID:DTXSID80161143
  • Nikkaji Number:J1.411.353C
  • Wikipedia:Diboron tetrafluoride
  • Wikidata:Q2183990
  • Mol file:13965-73-6.mol
Diboron tetrafluoride

Synonyms:Diboron tetrafluoride;13965-73-6;difluoroboranyl(difluoro)borane;difluoroboranyl-difluoro-borane;B2F4;Tetrafluorodiborane(4);Diborane(4), tetrafluoro-;DTXSID80161143;FT-0777907;Q2183990

Suppliers and Price of Diboron tetrafluoride
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 6 raw suppliers
Chemical Property of Diboron tetrafluoride Edit
Chemical Property:
  • Melting Point:-56°C 
  • Boiling Point:-34°C (estimate) 
  • PSA:0.00000 
  • Density:1.036g/cm3 
  • LogP:0.91920 
  • Water Solubility.:reac H2O [CRC10]Density, g/L: 3.990 [CRC10] 
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:0
  • Exact Mass:98.0122230
  • Heavy Atom Count:6
  • Complexity:26.5
Purity/Quality:

99%, *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:B(B(F)F)(F)F
Technology Process of Diboron tetrafluoride

There total 11 articles about Diboron tetrafluoride 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 neat (no solvent); byproducts: CBr3Cl; heating of B2F4 and CFBr3 in a sealed tube at 130°C for 2,5 h; fractionation at -160 and -95°C yielded B2F4;
Guidance literature:
In trichlorofluoromethane; byproducts: CCl4; B2Cl4 and 10-fold excess CCl3F were heated in a sealed tube at 90°C for 61 h; partially septd. by fractionation at -95 to -160°C; products detected by (19)F- and (11)B-NMR, CCl4 by (13)C-NMR;
Guidance literature:
byproducts: CBr4; B2Br4 and CFBr3 were reacted in a NMR-tube at ambient temp. for 9,75 h; products detected by (19)F- and (11)B-NMR, CBr4 by (13)C-NMR;
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