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681342 Sigma-Aldrich

Potassium (bromomethyl)trifluoroborate

90%

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Properties

Related Categories Alkyl Trifluoroborate Salts, Boronic Acids and Derivatives, Chemical Synthesis, Organometallic Reagents, Trifluoroborate Salts More...
Quality Level   100
assay   90%
mp   225-230 °C
SMILES string   [K+].F[B-](F)(F)CBr
InChI   1S/CH2BBrF3.K/c3-1-2(4,5)6;/h1H2;/q-1;+1
InChI key   AZDFPIRYUOCVCJ-UHFFFAOYSA-N

Description

Application

Organotrifluoroborate involved in:
• Suzuki-Miyaura cross-coupling reactions
• Synthesis of functionalized ethyltrifluoroborates
• SN2 displacement with alkoxides

Organotrifluoroborates as versatile and stable boronic acid surrogates.

Versatile starting material for preparation of a variety of functionalized substrates for Suzuki coupling.

Packaging

1, 5 g in poly bottle

Safety & Documentation

Safety Information

Symbol 
GHS07  GHS07
Signal word 
Warning
Hazard statements 
Precautionary statements 
Target organs 
Respiratory system
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
Peer-Reviewed Papers
15

References

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