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657093 Sigma-Aldrich

Potassium 3-formylphenyltrifluoroborate

95%

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Properties

Related Categories Aldehydes, Aryl Trifluoroborate Salts, Boronic Acids and Derivatives, Building Blocks, C7,
assay   95%
mp   >300 °C
SMILES string   [K+].F[B-](F)(F)c1cccc(C=O)c1
InChI   1S/C7H5BF3O.K/c9-8(10,11)7-3-1-2-6(4-7)5-12;/h1-5H;/q-1;+1
InChI key   ZUJWOVZZESBYHA-UHFFFAOYSA-N

Description

Packaging

1, 5 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

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Protocols & Articles

Articles

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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