Substance
ID:341767
Names and Identifiers
IUPAC name
(2-methylphenyl)boronic acid
IUPAC Traditional name
2-methylphenylboronic acid
Synonyms
o-Boronotolueneo-Tolueneboronic acid2-Methylphenylboronic acid邻甲基苯硼酸o-Methylphenylboronic acido-Tolylboronic acid(2-Tolyl)boronic acid2-Tolueneboronic acid2-甲基苯硼酸2-Methyl-1-phenylboronic acid2-Methylbenzeneboronic acid
Properties
Safety Information
GHS Signal Word
Warning
GHS Pictograms
Acute toxicity (oral, dermal, inhalation), category 4
Skin irritation, category 2
Eye irritation, category 2
Skin sensitisation, category 1
Specific Target Organ Toxicity – Single exposure, category 3
GHS Hazard statements
H315-H319-H335
European Hazard Symbols
Irritant (Xi)Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
GHS Precautionary statements
P261-P305+P351+P338
Risk Statements
36/37/38
MSDS Link
Safety Statements
26-36
German water hazard class
3
Product Information
Purity
≥95.0%
Linear Formula
CH3C6H4B(OH)2
Physical Property
Melting Point
162-164 °C(lit.)
Molecule Details
Other Notes
Contains varying amounts of anhydride
Packaging
1, 5, 25 g in glass bottle
Application
Reagent used for
• Palladium-catalyzed direct arylation of pyrazoles with phenylboronic acids1
• Pd-catalyzed arylation using Suzuki-Miyaura cross-coupling in water2
• Ruthenium catalyzed direct arylation reactions3
• Ligand-free copper-catalyzed coupling reactions4
• Copper-catalyzed cross-coupling reactions of diaryl diselenides5
• Phosphine-free Suzuki-Miyaura cross-coupling reactions6
• Rhodium-catalyzed asymmetric 1,4-addition reactions7 Reagent used in Preparation of
• Chiral monophosphorus ligands in asymmetric Suzuki-Miyaura coupling reaction8
• Palladium nanoparticles immobilized by click ionic copolymers as recyclable catalysts for Suzuki-Miyaura cross-coupling reaction in water9
• Human farnesyl pyrophosphate synthase inhibitors as antitumor agents for multiple myeloma cells10
Contains varying amounts of anhydride
Packaging
1, 5, 25 g in glass bottle
Application
Reagent used for
• Palladium-catalyzed direct arylation of pyrazoles with phenylboronic acids1
• Pd-catalyzed arylation using Suzuki-Miyaura cross-coupling in water2
• Ruthenium catalyzed direct arylation reactions3
• Ligand-free copper-catalyzed coupling reactions4
• Copper-catalyzed cross-coupling reactions of diaryl diselenides5
• Phosphine-free Suzuki-Miyaura cross-coupling reactions6
• Rhodium-catalyzed asymmetric 1,4-addition reactions7 Reagent used in Preparation of
• Chiral monophosphorus ligands in asymmetric Suzuki-Miyaura coupling reaction8
• Palladium nanoparticles immobilized by click ionic copolymers as recyclable catalysts for Suzuki-Miyaura cross-coupling reaction in water9
• Human farnesyl pyrophosphate synthase inhibitors as antitumor agents for multiple myeloma cells10
Molecular Spectra
No Data Available
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References
No Data Available
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