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2-Acetylbenzeneboronic acid, 97%
CAS: 308103-40-4 | C8H9BO3 | 163.97 g/mol
$305.40 - $1209.23
Chemical Identifiers
| CAS | 308103-40-4 |
|---|---|
| Molecular Formula | C8H9BO3 |
| Molecular Weight (g/mol) | 163.97 |
| MDL Number | MFCD01321263 |
| InChI Key | ZKAOVABYLXQUTI-UHFFFAOYSA-N |
| Synonym | 2-acetylphenyl boronic acid, boronic acid, 2-acetylphenyl, 2'-boronoacetophenone, 1-2-boronophenyl ethan-1-one, 2-acetylbenzeneboronic acid, 2-acetylbenzenboronicacid, 1-2-dihydroxyboranyl phenyl ethan-1-one, 2-acetylphenylboronicacid, pubchem5373, acmc-1agh6 |
| PubChem CID | 2734309 |
| IUPAC Name | (2-acetylphenyl)boronic acid |
| SMILES | CC(=O)C1=CC=CC=C1B(O)O |
| Catalog Number | Mfr. No. | Quantity | Price | Quantity | |||||
|---|---|---|---|---|---|---|---|---|---|
| Catalog Number | Mfr. No. | Quantity | Price | Quantity | |||||
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AAH2732706
|
Thermo Scientific Chemicals
H2732706 |
5 g |
Each for $305.40
|
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AAH2732714
|
Thermo Scientific Chemicals
H2732714 |
25 g |
Each for $1,209.23
|
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Description
2-Acetylphenylboronic acid is a reactant used for a variety of coupling reactions, as well as synthesis and hydroxy masking, Suzuki-Miyaura cross-coupling reactions, rhodium-catalyzed annulation of ynamides, transient masking of hydroxy groups, cationic palladium complex-catalyzed diastereoselective tandem annulation, hydrogen peroxide mediated formation of heteroaryl ethers and copper-catalyzed transmetalation and homocoupling.
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.
Applications2-Acetylphenylboronic acid is a reactant used for a variety of coupling reactions, as well as synthesis and hydroxy masking, Suzuki-Miyaura cross-coupling reactions, rhodium-catalyzed annulation of ynamides, transient masking of hydroxy groups, cationic palladium complex-catalyzed diastereoselective tandem annulation, hydrogen peroxide mediated formation of heteroaryl ethers and copper-catalyzed transmetalation and homocoupling.
Solubility
Slightly soluble in water.
Notes
Store away from oxidizing agents. Keep the container tightly closed and place it in a cool, dry and well ventilated condition.
Chemical Identifiers
| 308103-40-4 | |
| 163.97 | |
| ZKAOVABYLXQUTI-UHFFFAOYSA-N | |
| 2734309 | |
| CC(=O)C1=CC=CC=C1B(O)O |
| C8H9BO3 | |
| MFCD01321263 | |
| 2-acetylphenyl boronic acid, boronic acid, 2-acetylphenyl, 2'-boronoacetophenone, 1-2-boronophenyl ethan-1-one, 2-acetylbenzeneboronic acid, 2-acetylbenzenboronicacid, 1-2-dihydroxyboranyl phenyl ethan-1-one, 2-acetylphenylboronicacid, pubchem5373, acmc-1agh6 | |
| (2-acetylphenyl)boronic acid |
Specifications
| 308103-40-4 | |
| C8H9BO3 | |
| 5 g | |
| Slightly soluble in water. | |
| CC(=O)C1=CC=CC=C1B(O)O | |
| 163.97 | |
| 163.97 | |
| 2-Acetylbenzeneboronic acid |
| ∽170°C (decomposition) | |
| MFCD01321263 | |
| 2-acetylphenyl boronic acid, boronic acid, 2-acetylphenyl, 2'-boronoacetophenone, 1-2-boronophenyl ethan-1-one, 2-acetylbenzeneboronic acid, 2-acetylbenzenboronicacid, 1-2-dihydroxyboranyl phenyl ethan-1-one, 2-acetylphenylboronicacid, pubchem5373, acmc-1agh6 | |
| ZKAOVABYLXQUTI-UHFFFAOYSA-N | |
| (2-acetylphenyl)boronic acid | |
| 2734309 | |
| 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
TSCA : No
RUO – Research Use Only