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Borate(1-), tetrakis[4-(trifluoroMethyl)phenyl]-,sodiuM (1:1)

Base Information Edit
  • Chemical Name:Borate(1-), tetrakis[4-(trifluoroMethyl)phenyl]-,sodiuM (1:1)
  • CAS No.:22533-15-9
  • Molecular Formula:C28H16 B F12 . Na
  • Molecular Weight:614.217
  • Hs Code.:
  • Mol file:22533-15-9.mol
Borate(1-), tetrakis[4-(trifluoroMethyl)phenyl]-,sodiuM (1:1)

Synonyms:Borate(1-),tetrakis(a,a,a-trifluoro-p-tolyl)-, sodium (8CI); NSC 123497; Sodium tetrakis(4-trifluoromethylphenylborate)

Suppliers and Price of Borate(1-), tetrakis[4-(trifluoroMethyl)phenyl]-,sodiuM (1:1)
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 11 raw suppliers
Chemical Property of Borate(1-), tetrakis[4-(trifluoroMethyl)phenyl]-,sodiuM (1:1) Edit
Chemical Property:
  • Boiling Point:°Cat760mmHg 
  • Flash Point:°C 
  • PSA:0.00000 
  • Density:g/cm3 
  • LogP:9.96030 
Purity/Quality:

99%, *data from raw suppliers

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

SDS file from LookChem

Useful:
Technology Process of Borate(1-), tetrakis[4-(trifluoroMethyl)phenyl]-,sodiuM (1:1)

There total 2 articles about Borate(1-), tetrakis[4-(trifluoroMethyl)phenyl]-,sodiuM (1:1) 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 sodium hydroxide; In diethyl ether; below 25°C by the in situ method; reaction mixture is poured onto crushed ice made slightly alkaline with NaOH;
DOI:10.1016/S0003-2670(01)81750-5
Guidance literature:
In methanol; treating ammonium salt in methanol with NaOCH3 in anhydrous CH3OH; after removal of CH3OH at 70°C under vac.; residue is dissolved in ether and passed through filled column; the ether eluate is evapd. under vac. at 80°C; dried over P4O10 under vac. at 80°C;
DOI:10.1016/S0003-2670(01)81750-5
Guidance literature:
With triphenyl-arsane; palladium diacetate; diisopropylamine; In 1,4-dioxane; at 110 ℃; stereoselective reaction; Schlenk technique; Inert atmosphere; Sealed tube;
DOI:10.1039/d0ob01226b
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