missing translation for 'onlineSavingsMsg'
Learn More
  1. Home
  2. Products
  3. Chemicals
  4. Organic compounds
  5. Organic acids and derivatives
  6. Boronic acid derivatives
  7. 2-Methylbenzeneboronic acid, 98%

2-Methylbenzeneboronic acid, 98%

Product Code. 11456386
Change view
Click to view available options
Quantity:
1 g
5 g
25 g
Unit Size:
1g
25g
5g
3 product options available for selection
Product selection table with 3 available options. Use arrow keys to navigate and Enter or Space to select.
Product Code. Quantity unitSize
11456386 25 g 25g
11436386 1 g 1g
11446386 5 g 5g
Use arrow keys to navigate between rows. Press Enter or Space to select a product option. 3 options available.
3 options
This item is not returnable. View return policy
Product Code. 11456386 Supplier Thermo Scientific Alfa Aesar Supplier No. B23154.14
Request Bulk or Custom Formats

Please to purchase this item. Need a web account? Register with us today!

This item is not returnable. View return policy

Description

CAS: 16419-60-6 | C7H9BO2 | 135.96 g/mol

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.
TRUSTED_SUSTAINABILITY

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

Specifications

Melting Point ∼162°C to 164°C
Quantity 25 g
Beilstein 2935796
Solubility Information Slightly soluble in water.
Formula Weight 135.96
Percent Purity 98%
Chemical Name or Material 2-Methylbenzeneboronic acid

RUO – Research Use Only

Product Title
Select an issue

By clicking Submit, you acknowledge that you may be contacted by Fisher Scientific in regards to the feedback you have provided in this form. We will not share your information for any other purposes. All contact information provided shall also be maintained in accordance with our Privacy Policy.