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542458 Sigma-Aldrich

3-Isopropoxyphenylboronic acid

≥95%

Synonym: 3-(1-Methylethoxy)phenylboronic acid, 3-(1-Methylethyl)oxyphenylboronic acid, 3-Isopropoxybenzeneboronic 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   UKZVUHVNTYDSOP-UHFFFAOYSA-N
assay   ≥95%
form   powder
mp   76-81 °C (lit.)

Description

Application

Reactant for synthesis of:
• Heteroaryl benzylureas with glycogen synthase kinase 3 (GSK-3) inhibitory activity
• Modulators of survival motor neuron (SMN) protein
• Inhibitors of cholesteryl ester transfer protein (CETP)
• Selective sphingosine-1-phosphate receptor subtype-1 agonists
• Cytotoxic open lactone analogs of Lamellarin D

Packaging

1, 10 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

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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