2-Phenoxybenzeneboronic acid, 98%
2-Phenoxybenzeneboronic acid, 98%
2-Phenoxybenzeneboronic acid, 98%
Thermo Scientific Chemicals

2-Phenoxybenzeneboronic acid, 98%

CAS: 108238-09-1 | C12H11BO3 | 214.03 g/mol
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Quantity:
1 g
5 g
Catalog number H53264.03
also known as H53264-03
Price (USD)
40.20
Each
Quantity:
1 g
Request bulk or custom format
Price (USD)
40.20
Each
Chemical Identifiers
CAS108238-09-1
IUPAC Name(2-phenoxyphenyl)boronic acid
Molecular FormulaC12H11BO3
InChI KeyAVOWPOFIQZSVGV-UHFFFAOYSA-N
SMILESOB(O)C1=CC=CC=C1OC1=CC=CC=C1
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SpecificationsSpecification SheetSpecification Sheet
Assay (HPLC)≥97.5%
Appearance (Color)White
FormPowder
Proton NMR≥97.5% ¹H nmr
Reactant for palladium catalyzed cross-coupling reactions, trifluoromethylation via copper-mediated oxidative cross-coupling, preparation of biologically and pharmacologically active molecules, preparation of pyridazine-based scaffolds as a-helix mimetics.

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
Reactant for palladium catalyzed cross-coupling reactions, trifluoromethylation via copper-mediated oxidative cross-coupling, preparation of biologically and pharmacologically active molecules, preparation of pyridazine-based scaffolds as a-helix mimetics.

Solubility
Slightly soluble in water.

Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Store away from strong oxidizing agents.
RUO – Research Use Only
Bin, H.-R.; et al. Palladium-catalyzed peripheral arylation of 5-pyrazolones via enolizable bond protection Synthesis. 2011, volume 1783-1791.