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441686 Sigma-Aldrich

3-Methoxyphenylboronic acid

Synonym: (m-Methoxyphenyl)boronic acid, 3-Methoxybenzeneboronic acid, m-Methoxybenzeneboronic acid, m-Anisylboronic acid

  • CAS Number 10365-98-7

  • Linear Formula CH3OC6H4B(OH)2

  • Molecular Weight 151.96

  •  Beilstein/REAXYS Number 2831223

  •  MDL number MFCD00161359

  •  PubChem Substance ID 24867696

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Properties

Related Categories Aryl Boronic Acids, Boronic Acids, Boronic Acids and Derivatives, Chemical Synthesis, Monosubstituted Aryl Boronic Acids,
InChI Key   NLLGFYPSWCMUIV-UHFFFAOYSA-N
mp   160-163 °C (lit.)

Description

Packaging

1, 10 g in glass bottle

Other Notes

Contains varying amounts of anhydride

Safety & Documentation

Safety Information

Personal Protective Equipment 
RIDADR 
NONH for all modes of transport
WGK Germany 
3

Documents

Certificate of Analysis

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Certificate of Origin

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Protocols & Articles

Articles

Arylboronic Acids

We are 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 a cy...
ChemFiles 2001, 1.1, 5.
Keywords: Building blocks, Coupling reactions, Dehydration reaction, Suzuki coupling

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

Peer-Reviewed Papers
15

References

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