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597929 Sigma-Aldrich

Potassium 2,6-difluorophenyltrifluoroborate

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Properties

Related Categories Aryl Trifluoroborate Salts, Boronic Acids and Derivatives, Chemical Synthesis, Organometallic Reagents, Trifluoroborate Salts More...
InChI Key   XUCOCDVVPJFGSH-UHFFFAOYSA-N
mp   >300 °C (lit.)

Description

Packaging

5 g in poly bottle

Application

Reactant for:
• Iron-promoted hydrolysis
• Microwave-accelerated cross-coupling reactions
• Ligand- and base-free Suzuki-Miyaura cross-coupling under microwave irradiation
• Microwave-assisted amination

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

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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