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542504 Sigma-Aldrich

4-Butoxyphenylboronic 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   QUPFQMXWFNJUNJ-UHFFFAOYSA-N
mp   106-108 °C (lit.)

Description

General description

Contains varying amounts of anhydride.

Application

Reactant for:
• Suzuki-Miyaura cross-coupling reactions
• Condensation reactions
• Synthesis of azobenzene-functionalized compounds
• Preparation of highly fluorescent diketopyrrolopyrrole derivatives
• Rhodium-catalyzed Suzuki-type cross-coupling
• Copper-catalyzed asymmetric conjugate reduction of coumarins

Packaging

1 g in glass bottle

Safety & Documentation

Safety Information

RIDADR 
NONH for all modes of transport
WGK Germany 
3

Documents

Certificate of Analysis

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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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