190661-29-1
190661-29-1
Chemical Structure
2-Benzyloxyphenylboronic acid
- CAS No.: 190661-29-1
- Formula:C13H13BO3
- Molecular Weight:228.06
IUPAC Name: (2-(benzyloxy)phenyl)boronic acid
InChIKey: MCAIDINWZOCYQK-UHFFFAOYSA-N
SMILES: OB(O)C1=CC=CC=C1OCC2=CC=CC=C2
Biological Activity: 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].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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2-Benzyloxyphenylboronic acid | 99.65% | 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. | ||||||||||||||||||||
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References
- [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. [Content Brief]
