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4-Methoxybenzeneboronic acid, 97+%, Thermo Scientific Chemicals

Catalog Number 11481778
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Quantity:
1 g
5 g
25 g
This item is not returnable. View return policy
5720-07-0
C7H9BO3
151.96
MFCD00039139
VOAAEKKFGLPLLU-UHFFFAOYSA-N
4-methoxyphenyl boronic acid, 4-methoxybenzeneboronic acid, p-anisylboronic acid, p-methoxyphenylboronic acid, p-methoxybenzeneboronic acid, 4-methoxyphenyl boranediol, benzeneboronic acid, p-methoxy, 4-boronoanisole, 4-methoxyphenylboronicacid
201262
(4-methoxyphenyl)boronic acid
COC1=CC=C(C=C1)B(O)O
This item is not returnable. View return policy
5720-07-0
C7H9BO3
151.96
MFCD00039139
VOAAEKKFGLPLLU-UHFFFAOYSA-N
4-methoxyphenyl boronic acid, 4-methoxybenzeneboronic acid, p-anisylboronic acid, p-methoxyphenylboronic acid, p-methoxybenzeneboronic acid, 4-methoxyphenyl boranediol, benzeneboronic acid, p-methoxy, 4-boronoanisole, 4-methoxyphenylboronicacid
201262
(4-methoxyphenyl)boronic acid
COC1=CC=C(C=C1)B(O)O

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.
TRUSTED_SUSTAINABILITY
Melting Point 202°C to 208°C
Quantity 25 g
Beilstein 2936912
Solubility Information Soluble in dimethyl sulfoxide and methanol.
Formula Weight 151.96
Percent Purity ≥97%
Chemical Name or Material 4-Methoxybenzeneboronic acid

RUO – Research Use Only

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