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Sodium tetrakis[3,5-bis(trifluoromethyl)phenyl]borate

ALDRICH/692360

Synonym: Benzene, 1,3-bis(trifluoromethyl)-, boron complex; NaBARF; Tetrakis[3,5-bis(trifluoromethyl)phenyl]boron sodium

CAS Number: 79060-88-1
Empirical Formula (Hill Notation): C32H12BF24Na
Molecular Weight: 886.20
MDL Number: MFCD00043323
Linear Formula: C32H12BF24Na
Product Type: Chemical

Catalog Number PKG Qty. Price Quantity
45-692360-250MG 250 mg
$186.00
1/EA
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45-692360-1G 1 g
$361.00
1/EA
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This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material. This image depicts SKU: 692360-250MG

 

form powder
InChI 1S/C32H12BF24.Na/c34-25(35,36)13-1-14(26(37,38)39)6-21(5-13)33(22-7-15(27(40,41)42)2-16(8-22)28(43,44)45,23-9-17(29(46,47)48)3-18(10-23)30(49,50)51)24-11-19(31(52,53)54)4-20(12-24)32(55,56)57;/h1-12H;/q-1;+1
InChI key LTGMONZOZHXAHO-UHFFFAOYSA-N
reaction suitability core: sodium
  reagent type: catalyst
SMILES string [Na+].FC(F)(F)c1cc(cc(c1)C(F)(F)F)[B-](c2cc(cc(c2)C(F)(F)F)C(F)(F)F)(c3cc(cc(c3)C(F)(F)F)C(F)(F)F)c4cc(cc(c4)C(F)(F)F)C(F)(F)F
Application: The TFPB anion can be used to catalyze:

• In-situ diazo-coupling and N- and C-nitrosations.
• Synthesis of oxirane from different carbonyl substrates and trimethylsulfonium chloride via phase-transfer catalysis.
• Synthesis of ion selective membranes9
General description: Sodium tetrakis[3,5-bis(trifluoromethyl)phenyl]borate, also known as NaBArF, is widely used as a catalyst in the cyclopolymerization of functionalized trienes. NaBArF also acts as a precursor to synthesize other tetrakis[3,5-bis(trifluoromethyl)phenyl]borate (TFPB)-based reagents.Sodium tetrakis[3,5-bis(trifluoromethyl)phenyl]borate, also known as NaBAr′4, is a stable and highly soluble compound that has been used as a source of the [BArF] counterion in chemical synthesis. It has been found to be resistant to degradation by various oxidants and highly lipophilic. This compound has been used as a convenient reagent for the generation and stabilization of cationic electrophilic metal alkyl complexes. It has also been used in the living polymerization of ethylene, oligomerization of α-olefins, and olefin hydrogenation and hydrosilylation.
Packaging: 1 g in glass bottle
Packaging: 250 mg in glass bottle
RIDADR NONH for all modes of transport
WGK Germany WGK 3
Flash Point(F) Not applicable
Flash Point(C) Not applicable
UNSPSC 12161600

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