missing translation for 'onlineSavingsMsg'
Learn More
Please login to your online account to display your discounted pricing

2-Methylbenzeneboronic acid, 98%, Thermo Scientific Chemicals

$77.82 - $515.47

Chemical Identifiers

CAS 16419-60-6
Molecular Formula C7H9BO2
Molecular Weight (g/mol) 135.96
MDL Number MFCD00093526
InChI Key NSJVYHOPHZMZPN-UHFFFAOYSA-N
Synonym 2-tolylboronic acid, o-tolylboronic acid, 2-methylbenzeneboronic acid, 2-methylphenyl boronic acid, o-methylphenylboronic acid, 2-methylphenyl boranediol, tolylboronic acid, o-tolueneboronic acid, toluene-2-boronic acid, boronic acid, methylphenyl
PubChem CID 2733267
IUPAC Name (2-methylphenyl)boronic acid
SMILES CC1=CC=CC=C1B(O)O
View More Specs

Products 3
Catalog Number Mfr. No. Quantity Price Quantity  
Catalog Number Mfr. No. Quantity Price Quantity  
AAB2315403
View Documents
Thermo Scientific Chemicals
B2315403
1 g
Each for $77.82
 
AAB2315406
View Documents
Thermo Scientific Chemicals
B2315406
5 g
Each for $171.51
 
AAB2315414
View Documents
Thermo Scientific Chemicals
B2315414
25 g
Each for $515.47
 
Description

Description

2-Methylbenzeneboronic acid is a reagent used for Pd-catalyzed arylation using Suzuki-Miyaura cross-coupling in water, Ruthenium catalyzed direct arylation reactions, Ligand-free copper-catalyzed coupling reactions, Rhodium-catalyzed asymmetric 1,4-addition reactions. Reagent used in Preparation of chiral monophosphorus ligands in asymmetric Suzuki-Miyaura coupling reaction, Human farnesyl pyrophosphate synthase inhibitors as antitumor agents for multiple myeloma cells

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
2-Methylbenzeneboronic acid is a reagent used for Pd-catalyzed arylation using Suzuki-Miyaura cross-coupling in water, Ruthenium catalyzed direct arylation reactions, Ligand-free copper-catalyzed coupling reactions, Rhodium-catalyzed asymmetric 1,4-addition reactions. Reagent used in Preparation of chiral monophosphorus ligands in asymmetric Suzuki-Miyaura coupling reaction, Human farnesyl pyrophosphate synthase inhibitors as antitumor agents for multiple myeloma cells

Solubility
Slightly soluble in water.

Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Incompatible with oxidizing agent.
Specifications

Chemical Identifiers

16419-60-6
135.96
NSJVYHOPHZMZPN-UHFFFAOYSA-N
2733267
CC1=CC=CC=C1B(O)O
C7H9BO2
MFCD00093526
2-tolylboronic acid, o-tolylboronic acid, 2-methylbenzeneboronic acid, 2-methylphenyl boronic acid, o-methylphenylboronic acid, 2-methylphenyl boranediol, tolylboronic acid, o-tolueneboronic acid, toluene-2-boronic acid, boronic acid, methylphenyl
(2-methylphenyl)boronic acid

Specifications

16419-60-6
C7H9BO2
1 g
2-tolylboronic acid, o-tolylboronic acid, 2-methylbenzeneboronic acid, 2-methylphenyl boronic acid, o-methylphenylboronic acid, 2-methylphenyl boranediol, tolylboronic acid, o-tolueneboronic acid, toluene-2-boronic acid, boronic acid, methylphenyl
NSJVYHOPHZMZPN-UHFFFAOYSA-N
(2-methylphenyl)boronic acid
2733267
98%
∼162°C to 164°C
MFCD00093526
2935796
Slightly soluble in water.
CC1=CC=CC=C1B(O)O
135.96
135.96
2-Methylbenzeneboronic acid
Videos
Safety and Handling

Safety and Handling

GHS H Statement
H315-H319-H335
Causes skin irritation.
Causes serious eye irritation.
May cause respiratory irritation.

P261-P264b-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P312-P330-P332+P313-P362-P501c

H302-H315-H319-H335

EINECSNumber : 000-000-0

RTECSNumber : ED7777777

TSCA : No

Recommended Storage : Ambient temperatures

SDS
missing translation for 'documents'

missing translation for 'documents'

RUO – Research Use Only