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524697 Sigma-Aldrich

2,3,5-Trifluorophenylboronic acid

≥95%

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Properties

Related Categories Aryl Boronic Acids, Boronic Acids, Boronic Acids and Derivatives, Chemical Synthesis, Organometallic Reagents,
Quality Level   100
assay   ≥95%
mp   221 °C (dec.) (lit.)
SMILES string   OB(O)c1cc(F)cc(F)c1F
InChI   1S/C6H4BF3O2/c8-3-1-4(7(11)12)6(10)5(9)2-3/h1-2,11-12H
InChI key   IRMUMGKQAXLGHK-UHFFFAOYSA-N

Description

Application

Reactant involved in the synthesis of biologically active compounds:
• Pyrazole-acids to be used as agonists of human orphan GPCR GPR109a
• Bicyclic pyrazole carboxylic acid derivatives as a niacin receptor agonist
• 5-Alkyl and 5-aryl-pyrazole-tetrazoles as agonists of human orphan GPCR GPR109a

Packaging

5 g in glass bottle

Other Notes

Contains varying amounts of anhydride

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

Articles

Boronic Acids - ChemFiles 2007

Most boronic acids readily undergo dehydration reactions to give a cyclic (trimer) anhydride. Our selection of boronic acids may contain varying amounts of this cyclic anhydride. Fortunately, the aci...
ChemFiles 2007, 7.7, 3.
Keywords: Coupling reactions, Dehydration reaction, Suzuki coupling

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