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4-Methoxybenzeneboronic acid, 97+%, Thermo Scientific Chemicals
43.42 € - 401.00 €
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 |
Product Code | Brand | Quantity | Price | Quantity & Availability | |||||
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Product Code | Brand | Quantity | Price | Quantity & Availability | |||||
11461778
|
Thermo Scientific Alfa Aesar
A14462.03 |
1 g |
43.42 €
1g |
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11471778
|
Thermo Scientific Alfa Aesar
A14462.06 |
5 g |
168.84 €
5g |
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11481778
|
Thermo Scientific Alfa Aesar
A14462.14 |
25 g |
401.00 €
25g |
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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.
Applications4-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.
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% |
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
RUO – Research Use Only