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4-Bromobenzeneboronic acid, 97+%
CAS: 5467-74-3 | C6H6BBrO2 | 200.83 g/mol
$45.73 - $690.23
Chemical Identifiers
| CAS | 5467-74-3 |
|---|---|
| Molecular Formula | C6H6BBrO2 |
| Molecular Weight (g/mol) | 200.83 |
| MDL Number | MFCD00002104 |
| InChI Key | QBLFZIBJXUQVRF-UHFFFAOYSA-N |
| Synonym | 4-bromophenyl boronic acid, 4-bromobenzeneboronic acid, 4-bromophenylboric acid, p-bromophenylboronic acid, p-bromophenylboric acid, p-bromobenzeneboronic acid, boronic acid, 4-bromophenyl, benzeneboronic acid, p-bromo, p-bromophenyl boronic acid, 4-bromo phenyl boronic acid |
| PubChem CID | 79599 |
| IUPAC Name | (4-bromophenyl)boronic acid |
| SMILES | OB(O)C1=CC=C(Br)C=C1 |
| Catalog Number | Mfr. No. | Quantity | Price | Quantity | |||||
|---|---|---|---|---|---|---|---|---|---|
| Catalog Number | Mfr. No. | Quantity | Price | Quantity | |||||
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AAL0156503
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Thermo Scientific Chemicals
L0156503 |
1 g |
Each for $45.73
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AAL0156506
|
Thermo Scientific Chemicals
L0156506 |
5 g |
Each for $145.81
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AAL0156514
|
Thermo Scientific Chemicals
L0156514 |
25 g |
Each for $690.23
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Description
4-Bromobenzeneboronic acid is a reagent used for Palladium catalyzed Suzuki-Miyaura cross-couplings, Tandem-type Pd(II)-catalyzed oxidative Heck reaction and intramolecular C-H amidation sequence. It is also used in the preparation of Protein modulators and enzymatic and kinase inhibitors, Gallate-based obovatol analogs with potential anti-tumor activity. It is used as a reagent for Copper-mediated ligandless aerobic fluoroalkylation of arylboronic acids with fluoroalkyl iodides, Pd-catalyzed arylative cyclization of alkyne-tethered enals or enones via carbopalladation of alkynes, Copper-catalyzed cross-couplings.
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-Bromobenzeneboronic acid is a reagent used for Palladium catalyzed Suzuki-Miyaura cross-couplings, Tandem-type Pd(II)-catalyzed oxidative Heck reaction and intramolecular C-H amidation sequence. It is also used in the preparation of Protein modulators and enzymatic and kinase inhibitors, Gallate-based obovatol analogs with potential anti-tumor activity. It is used as a reagent for Copper-mediated ligandless aerobic fluoroalkylation of arylboronic acids with fluoroalkyl iodides, Pd-catalyzed arylative cyclization of alkyne-tethered enals or enones via carbopalladation of alkynes, Copper-catalyzed cross-couplings.
Solubility
Soluble in methanol. Insoluble in water.
Notes
Store in a cool and dark place. Store away from incompatible materials such as oxidizing agents. Incompatible with Oxidizing agents, Acids, Bases, Alcohols
Chemical Identifiers
| 5467-74-3 | |
| 200.83 | |
| QBLFZIBJXUQVRF-UHFFFAOYSA-N | |
| 79599 | |
| OB(O)C1=CC=C(Br)C=C1 |
| C6H6BBrO2 | |
| MFCD00002104 | |
| 4-bromophenyl boronic acid, 4-bromobenzeneboronic acid, 4-bromophenylboric acid, p-bromophenylboronic acid, p-bromophenylboric acid, p-bromobenzeneboronic acid, boronic acid, 4-bromophenyl, benzeneboronic acid, p-bromo, p-bromophenyl boronic acid, 4-bromo phenyl boronic acid | |
| (4-bromophenyl)boronic acid |
Specifications
| 5467-74-3 | |
| C6H6BBrO2 | |
| 1 g | |
| 4-bromophenyl boronic acid, 4-bromobenzeneboronic acid, 4-bromophenylboric acid, p-bromophenylboronic acid, p-bromophenylboric acid, p-bromobenzeneboronic acid, boronic acid, 4-bromophenyl, benzeneboronic acid, p-bromo, p-bromophenyl boronic acid, 4-bromo phenyl boronic acid | |
| QBLFZIBJXUQVRF-UHFFFAOYSA-N | |
| (4-bromophenyl)boronic acid | |
| 79599 | |
| ≥97% |
| 282°C to 286°C | |
| MFCD00002104 | |
| 2936347 | |
| Soluble in methanol. Insoluble in water. | |
| OB(O)C1=CC=C(Br)C=C1 | |
| 200.83 | |
| 200.83 | |
| 4-Bromobenzeneboronic 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
EINECSNumber : 226-779-9
RTECSNumber : CY8650000
TSCA : No
Recommended Storage : Ambient temperatures
RUO – Research Use Only