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4-Methoxybenzeneboronic acid, 97+%, Thermo Scientific Chemicals
$66.05 - $643.49
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 |
| Catalog Number | Mfr. No. | Quantity | Price | Quantity | |||||
|---|---|---|---|---|---|---|---|---|---|
| Catalog Number | Mfr. No. | Quantity | Price | Quantity | |||||
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AAA1446203
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Thermo Scientific Chemicals
A1446203 |
1 g |
Each for $66.05
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AAA1446206
|
Thermo Scientific Chemicals
A1446206 |
5 g |
Each for $171.51
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AAA1446214
|
Thermo Scientific Chemicals
A1446214 |
25 g |
Each for $643.49
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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 | |
| 1 g | |
| 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% |
| 202°C to 208°C | |
| MFCD00039139 | |
| 2936912 | |
| Soluble in dimethyl sulfoxide and methanol. | |
| COC1=CC=C(C=C1)B(O)O | |
| 151.96 | |
| 151.96 | |
| 4-Methoxybenzeneboronic acid |
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
RTECSNumber : CY8975000
TSCA : No
Recommended Storage : Ambient temperatures
RUO – Research Use Only