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
製品番号(カタログ番号) H53264.06
または、製品番号H53264-06
価格(JPY)
-
数量:
5 g
一括またはカスタム形式をリクエストする
化学物質識別子
CAS108238-09-1
IUPAC Name(2-phenoxyphenyl)boronic acid
Molecular FormulaC12H11BO3
InChI KeyAVOWPOFIQZSVGV-UHFFFAOYSA-N
SMILESOB(O)C1=CC=CC=C1OC1=CC=CC=C1
さらに表示
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.