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718572 Sigma-Aldrich

Potassium [4-(phenylaminomethyl)phenyl]trifluoroborate

97%

  • Empirical Formula (Hill Notation) C13H12BF3KN

  • Molecular Weight 289.15

  •  MDL number MFCD11052774

  •  PubChem Substance ID 329763590

  •  NACRES NA.22

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Properties

Related Categories Aryl Trifluoroborate Salts, Boronic Acids and Derivatives, Chemical Synthesis, Organometallic Reagents, Trifluoroborate Salts More...
Quality Level   100
assay   97%
mp   254-258 °C
SMILES string   [K+].F[B-](F)(F)c1ccc(CNc2ccccc2)cc1
InChI   1S/C13H12BF3N.K/c15-14(16,17)12-8-6-11(7-9-12)10-18-13-4-2-1-3-5-13;/h1-9,18H,10H2;/q-1;+1
InChI key   GLMXEGXYEWHGJO-UHFFFAOYSA-N

Description

Packaging

1 g in glass bottle

Safety & Documentation

Safety Information

Symbol 
GHS07  GHS07
Signal word 
Warning
Hazard statements 
Precautionary statements 
RIDADR 
NONH for all modes of transport
WGK Germany 
WGK 3
Flash Point(F) 
Not applicable
Flash Point(C) 
Not applicable

Documents

Certificate of Analysis (COA)

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Protocols & Articles

Articles

Organotrifluoroborates as Coupling Partners in Suzuki-Miyaura Reactions

Suzuki-Miyaura cross-coupling reactions are some of the most common methods for the formation of C–C bonds in organic chemistry. The use of some boronic acids is complicated by their instability and ...
Josephine Nakhla
Chemfiles Volume 10 Article 3
Keywords: Addition reactions, Chemfiles, Coupling reactions, Cross couplings, Methods, Precipitation

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