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510122 Aldrich

3-(Trifluoromethoxy)phenylboronic acid

Synonym: 3-Trifluoromethoxybenzeneboronic acid

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Properties

Related Categories Aryl Boronic Acids, Boronic Acids, Boronic Acids and Derivatives, Chemical Synthesis, Monosubstituted Aryl Boronic Acids,
InChI Key   UWDFWVLAHRQSKK-UHFFFAOYSA-N
mp   84-89 °C(lit.)

Description

Other Notes

Contains varying amounts of anhydride

Packaging

5 g in glass bottle

Application

Precursor commonly used in the synthesis of biologically active compounds including:
• Multisubstituted purines for use as P2X7 antagonists in the treatment of pain
• Heteroaryl substituted tetrahydropyrroloijquinolinone derivatives as aldosterone synthase inhibitors
• Fluorohydroquinolineethanol as a CETP inhibitor
• Biaryl amides with muscarinic acetylcholine receptor subtype M1 agonist activity
• C2-aryl pyrrolobenzodiasepine antitumor agents
• Piperazine-bisamide for obesity treatments

Price and Availability


Cross-Coupling Guide
Safety & Documentation

Safety Information

RIDADR 
NONH for all modes of transport
WGK Germany 
3
Protocols & Articles

Articles

Arylboronic Acids

Aldrich is pleased to present its complete selection of arylboronic acids, the building blocks of the Suzuki coupling experiment. Most arylboronic acids readily undergo dehydration reactions to give ...
Aldrich ChemFiles 2001, 1.1, 5.
Keywords: Building blocks, Coupling reactions, Dehydration reaction, Suzuki coupling

Boronic Acids

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...
Aldrich ChemFiles 2007, 7.7, 3.
Keywords: Chemfiles, Coupling reactions, Dehydration reaction, Suzuki coupling

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