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637890 Sigma-Aldrich

Potassium methyltrifluoroborate

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Properties

Related Categories Alkyl Trifluoroborate Salts, Boronic Acids and Derivatives, Chemical Synthesis, Organometallic Reagents, Trifluoroborate Salts More...
Quality Level   100
impurities   ≤2 mol water
mp   168-183 °C
SMILES string   [K+].C[B-](F)(F)F
InChI   1S/CH3BF3.K/c1-2(3,4)5;/h1H3;/q-1;+1
InChI key   XMQFVHVGFQJMFF-UHFFFAOYSA-N

Description

Application

Reactant for:
• Preparation of modified purines via palladium-catalyzed cross-coupling reactions with halopurines
• Suzuki-Miyaura cross-coupling reactions with aryl chlorides

Packaging

1, 5 g in glass bottle

Safety & Documentation

Safety Information

Personal Protective Equipment 
RIDADR 
NONH for all modes of transport
WGK Germany 
WGK 3
Flash Point(F) 
Not applicable
Flash Point(C) 
Not applicable
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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