2-Benzyloxyphenylboronic acid

2-Benzyloxyphenylboronic acid is a biochemical reagent that can be used as a biological material or organic compound for life science related research. 2-Benzyloxyphenylboronic acid is also a substrate used in asymmetric Suzuki coupling reactions. 2-Benzyloxyphenylboronic acid can be utilized in the synthesis of other active compounds[1][2].

Product Specifications

CAS Number

[190661-29-1]

UNSPSC

12352200

Hazard Statement

H302, H315, H319, H335

Target

Biochemical Assay Reagents

Type

Biochemical Assay Reagents

Related Pathways

Others

Field of Research

Others

Assay Protocol

https://www.medchemexpress.com/2-benzyloxyphenylboronic-acid.html

Purity

99.66

Solubility

10 mM in DMSO

Smiles

OB(O)C1=CC=CC=C1OCC2=CC=CC=C2

Molecular Formula

C13H13BO3

Molecular Weight

228.06

Precautions

H302, H315, H319, H335

References & Citations

[1]Zhang Y, et al. Enantioselective Syntheses of Axially Chiral Phosphonates or Phosphine Oxides via Asymmetric Suzuki Reactions with Chiral Sulfinamide Monophosphine Ligands. ChemistrySelect, 2019, 4 (17) : 5122-5125.|[2]Presset M, et al. Copper-mediated radical trifluoromethylation of unsaturated potassium organotrifluoroborates. J Org Chem. 2013 Dec 20;78 (24) :12837-43.