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654728 Sigma-Aldrich

Potassium 4-tert-butylphenyltrifluoroborate

95%

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Properties

Related Categories Aryl Trifluoroborate Salts, Boronic Acids and Derivatives, Chemical Synthesis, Organometallic Reagents, Trifluoroborate Salts More...
assay   95%
mp   >230 °C (lit.)
SMILES string   [K+].CC(C)(C)c1ccc(cc1)[B-](F)(F)F
InChI   1S/C10H13BF3.K/c1-10(2,3)8-4-6-9(7-5-8)11(12,13)14;/h4-7H,1-3H3;/q-1;+1
InChI key   RQPOMNZPBPIWDB-UHFFFAOYSA-N

Description

Packaging

1, 10 g in poly bottle

Safety & Documentation

Safety Information

Symbol 
GHS05  GHS05
Signal word 
Danger
Hazard statements 
Precautionary statements 
RIDADR 
UN 3261 8 / PGII
WGK Germany 
3
Protocols & Articles

Articles

New Trifl uoroborate Salts for Suzuki Coupling from Aldrich R&D

Trifluoroborates are air-stable alternatives to boronic acids in palladium-catalyzed Suzuki–Miyaura cross-coupling reactions.1,2 They are more robust, easier to handle, and less prone to protodeboron...
Aldrich ChemFiles 2005, 5.5, 11.
Keywords: Catalysis, Chemfiles, Coupling reactions, Cross couplings

Potassium Trifluoroborate Salts

Boronic acids, boronate esters, and organoboranes have been utilized for many years as the primary boron source in Suzuki–Miyaura-type reactions. These organoboron reagents have inherent limitations ...
ChemFiles Volume 5 Article 10
Keywords: Aldrichimica Acta, Coupling reactions, Cross couplings, Degradations, Epoxidations, Type

Professor and Product Portal - Gary Molander Group

From our library of Articles, Sigma-Aldrich presents Professor and Product Portal - Gary Molander Group
Keywords: Catalysis, Coupling reactions, Cross couplings, Transmetalation

Related Content

Organotrifluoroborates in Chemical Synthesis

Potent Boronic Acid Surrogates In the vast array of catalytic carbon-carbon bond forming reactions, the Suzuki-Miyaura protocol has proven to be a particularly attractive method.  The organoborane nu...
Keywords: Addition reactions, Catalysis, Coupling reactions, Cross couplings, Halogenations, Suzuki-Miyaura coupling

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