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598062 Sigma-Aldrich

3,5-Dimethyl-4-methoxyphenylboronic acid

≥95%

Synonym: 4-Methoxy-3,5-dimethylbenzeneboronic acid, 4-Methoxy-3,5-dimethylphenylboronic acid

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Properties

Related Categories Aryl Boronic Acids, Boronic Acids, Boronic Acids and Derivatives, Chemical Synthesis, Organometallic Reagents,
assay   ≥95%
mp   235-242 °C (lit.)
SMILES string   COc1c(C)cc(cc1C)B(O)O
InChI   1S/C9H13BO3/c1-6-4-8(10(11)12)5-7(2)9(6)13-3/h4-5,11-12H,1-3H3
InChI key   WZUCSPWZHRVOSD-UHFFFAOYSA-N

Description

Application

Reactant for:
• Preparation of biologically and pharmacologically active molecules
• Suzuki and Stille cross-coupling reaction
• Mizoroki-Heck arylation
• Baeyer-Villiger oxidation
• Rhodium-catalyzed asymmetric conjugate addition reactions

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
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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