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4-Methoxybenzeneboronic acid, 97+%, Thermo Scientific Chemicals
Catalog number: A14462.03
1 g, Each
Thermo Scientific Chemicals
4-Methoxybenzeneboronic acid, 97+%, Thermo Scientific Chemicals
Catalog number: A14462.03
1 g, Each
Quantity
Catalog number: A14462.03
also known as A14462-03
Price (USD)
37.20
Each
Quantity
-
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Chemical Identifiers
CAS
5720-07-0
IUPAC Name
(4-methoxyphenyl)boronic acid
Molecular Formula
C7H9BO3
InChI Key
VOAAEKKFGLPLLU-UHFFFAOYSA-N
SMILES
COC1=CC=C(C=C1)B(O)O
Specifications
Specification SheetAssay (Aqueous acid-base Titration)
≥97.0%
Assay (HPLC)
≥97.0%
Identification (FTIR)
Conforms
Proton NMR
Conforms to structure
Appearance (Color)
White to pale cream to pale brown
Description
4-Methoxybenzeneboronic acid is used for Suzuki-Miyaura cross-coupling reactions, Pd-catalyzed direct arylation, Highly effective synthesis using palladium-catalyzed arylation Suzuki-Miyaura cross-coupling in water, Palladium-catalyzed stereoselective Heck-type reaction, Tandem-type Pd(II)-catalyzed oxidative Heck reaction and intramolecular C-H amidation sequence, Copper-mediated ligandless aerobic fluoroalkylation of arylboronic acids with fluoroalkyl iodides, Ruthenium catalyzed direct arylation, Rh-catalyzed asymmetric conjugate addition, Ligand-free copper-catalyzed coupling.
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
4-Methoxybenzeneboronic acid is used for Suzuki-Miyaura cross-coupling reactions, Pd-catalyzed direct arylation, Highly effective synthesis using palladium-catalyzed arylation Suzuki-Miyaura cross-coupling in water, Palladium-catalyzed stereoselective Heck-type reaction, Tandem-type Pd(II)-catalyzed oxidative Heck reaction and intramolecular C-H amidation sequence, Copper-mediated ligandless aerobic fluoroalkylation of arylboronic acids with fluoroalkyl iodides, Ruthenium catalyzed direct arylation, Rh-catalyzed asymmetric conjugate addition, Ligand-free copper-catalyzed coupling.
Solubility
Soluble in dimethyl sulfoxide and methanol.
Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place.
4-Methoxybenzeneboronic acid is used for Suzuki-Miyaura cross-coupling reactions, Pd-catalyzed direct arylation, Highly effective synthesis using palladium-catalyzed arylation Suzuki-Miyaura cross-coupling in water, Palladium-catalyzed stereoselective Heck-type reaction, Tandem-type Pd(II)-catalyzed oxidative Heck reaction and intramolecular C-H amidation sequence, Copper-mediated ligandless aerobic fluoroalkylation of arylboronic acids with fluoroalkyl iodides, Ruthenium catalyzed direct arylation, Rh-catalyzed asymmetric conjugate addition, Ligand-free copper-catalyzed coupling.
Solubility
Soluble in dimethyl sulfoxide and methanol.
Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place.
RUO – Research Use Only
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