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571563 Sigma-Aldrich

Potassium 3,5-bis(trifluoromethyl)phenyltrifluoroborate

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Properties

Related Categories Aryl Trifluoroborate Salts, Boronic Acids and Derivatives, Chemical Synthesis, Organometallic Reagents, Trifluoroborate Salts More...
SMILES string   [K+].F[B-](F)(F)c1cc(cc(c1)C(F)(F)F)C(F)(F)F
InChI   1S/C8H3BF9.K/c10-7(11,12)4-1-5(8(13,14)15)3-6(2-4)9(16,17)18;/h1-3H;/q-1;+1
InChI key   WCHMTVMZBOZGCS-UHFFFAOYSA-N

Description

Packaging

1 g in poly bottle

Safety & Documentation

Safety Information

Symbol 
GHS07  GHS07
Signal word 
Warning
Hazard statements 
Precautionary statements 
Personal Protective Equipment 
RIDADR 
NONH for all modes of transport
WGK Germany 
3
Protocols & Articles

Articles

Chemfiles Volume 4 Article 2 - Potassium Trifluoroborates

Alkyl, aryl, and alkenyl trifluoroborate salts are compelling alternatives to boronic acids in Suzuki–Miyaura coupling and in rhodium catalyzed carbon-carbon bond forming reactions. These salts are a...
Chemfiles Volume 4 Article 2
Keywords: Catalysis, Cross couplings, Ligands

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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