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Purity 98% 2 3 4 5 6 Pentafluorophenyl Borane CAS No 1109-15-5

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Product Details

Mat no.10011001 Tris(2,3,4,5,6-pentafluorophenyl)borane CAS No.1109-15-5 White to light yellow Powder Purity 98%

Basic information of Tris(2,3,4,5,6-pentafluorophenyl)borane

English synonyms PERFLUOROTRIPHENYLBORANE ; TRIS(PENTAFLUOROPHENYL)BORANE ; TRIS(PENTAFLUOROPHENYL)BORON ; Tris(2,3,4,5,6-pentafluorophenyl)borane ; TRIS(PENTAFLUOROPHENYL)BORANE SOLUTION, ~3% IN ISOPAR TORRIS,HENENTBOLUTION, ~3% IN ISOPAR ; TORRIS(PENTAFLUOROPHENYL) +% ; Tris(Pentafluorophenyl)Borate ; Tris(pentafluorophenyl)boron,min.97%
CAS No. 1109-15-5
Molecular formula C18BF15
Molecular weight 511.98


Tris(2,3,4,5,6-pentafluorophenyl)borane properties

Melting point 126-131 °C (lit.)
Boiling point 327.3±42.0 °C(Predicted)
density 0.73 g/mL at 20 °C
Refractive index n20/D 1.41
Flash point 7 °C
Storage conditions Inert atmosphere,Store in freezer, under -20°C
Solubility Soluble in hexane, chloroform, dichloromethane, toluene, and polar solvents.
form Powder
color White to light yellow-beige
proportion 1.7
Maximum wavelength (λmax) 306nm(Toluene)(lit.)
Sensitivity Moisture Sensitive
Hydrolysis sensitivity 4: no reaction with water under neutral conditions
Merck 14,9755
BRN 2931347

 

Use and production method of Tris(2,3,4,5,6-pentafluorophenyl)borane

Introduction Trans (pentafluorophenyl) boron is also called tris (pentafluorophenyl) borane. Compared with traditional Lewis acid, it has the advantages of stable chemical properties, strong acidity and convenient use. It is called non-traditional Lewis chemical Book acid. The application field of trans (pentafluorophenyl) boron has developed from the initial olefin polymerization Co catalyst to other fields of organic chemistry and polymer chemistry. The reaction catalyzed by tris (pentafluorophenyl) borane is very different from that catalyzed by traditional Lewis acid in reaction mechanism and reaction results.
use

Common reagents are used to prepare d0 aromatics and other organometallic complexes, as well as polymerization catalysts.

Production method After adding pentafluorobromobenzene (0.09mol, 22.2g) into a three port bottle (250ml), add 2 ‑ methyltetrahydrofuran (100ml). N ‑ Buli (2.5m, 0.09mol, 36ml) was added dropwise at 25 ℃. After 6.0h of reaction, trimethyl borate (0.03mol, 3.1g) was added dropwise at 25 ℃ for 10min. After 16 chemicalbookh at 25 ℃, the reaction was monitored by GC. Pour the reaction solution into water, extract it with 2 ‑ methyltetrahydrofuran twice, combine the organic layer, wash it with water twice, wash it with saturated salt water once, dry the organic layer with sodium sulfate, evaporate 2 ‑ methyltetrahydrofuran under reduced pressure, and recover 2 ‑ methyltetrahydrofuran to obtain crude product. Recrystallize with n-hexane to obtain trans (pentafluorobenzene) boron (0.0049mol, 2.48g), with a yield of 16.2%.

 

Security Information

Dangerous Goods Sign Xi,T,N,Xn,F
Dangerous goods transport number UN 1268 3/PG 2
WGK Germany 3
TSCA No
HazardClass 6.1
HS code 29039990




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