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557706 Sigma-Aldrich

4-Propoxyphenylboronic 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   SOKFEJKZYHYKSY-UHFFFAOYSA-N
mp   123-126 °C (lit.)

Description

Application

Reactant for:
• Synthesis of obovatol derivatives as anti-platelet activity
• Suzuki-Miyaura reaction with chloro arenes using (phenylphosphine)palladium catalyst
• Preparation of bisaryl substituted thiazoles and oxazoles as selective peroxisome proliferator-activated receptor δ (PPARδ) agonists
• Selective BACE1 inhibitors using regioselective Suzuki coupling
• Preparation of dichroic fluorescent benzothiadiazole dyes

Packaging

5 g in glass bottle

Other Notes

Contains varying amounts of anhydride.

Safety & Documentation

Safety Information

RIDADR 
NONH for all modes of transport
WGK Germany 
3
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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