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

47.50 EUR - 439.00 EUR

Chemical Identifiers

CAS 5720-07-0
Molecular Formula C7H9BO3
Molecular Weight (g/mol) 151.96
MDL Number MFCD00039139
InChI Key VOAAEKKFGLPLLU-UHFFFAOYSA-N
Synonym 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
PubChem CID 201262
IUPAC Name (4-methoxyphenyl)boronic acid
SMILES COC1=CC=C(C=C1)B(O)O
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Products 3
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Thermo Scientific Alfa Aesar
A14462.03
1 g
47.50 EUR
1g
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Thermo Scientific Alfa Aesar
A14462.06
5 g
185.00 EUR
5g
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Thermo Scientific Alfa Aesar
A14462.14
25 g
439.00 EUR
25g
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Description

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.
Specifications

Chemical Identifiers

5720-07-0
151.96
VOAAEKKFGLPLLU-UHFFFAOYSA-N
201262
COC1=CC=C(C=C1)B(O)O
C7H9BO3
MFCD00039139
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
(4-methoxyphenyl)boronic acid

Specifications

5720-07-0
C7H9BO3
2936912
Soluble in dimethyl sulfoxide and methanol.
COC1=CC=C(C=C1)B(O)O
151.96
151.96
4-Methoxybenzeneboronic acid
202°C to 208°C
MFCD00039139
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
VOAAEKKFGLPLLU-UHFFFAOYSA-N
(4-methoxyphenyl)boronic acid
201262
≥97%
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Safety and Handling

Safety and Handling

GHS H Statement
H315-H319-H335
Causes skin irritation.
Causes serious eye irritation.
May cause respiratory irritation.

P261-P264b-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P332+P313-P362-P501c

H315-H319-H335

missing translation for 'rtecsNumber' : CY8975000

missing translation for 'tsca' : No

Recommended Storage : Ambient temperatures

SDS
Documents

Documents

Product Certifications

RUO – Research Use Only