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

Catalog Number p-7043609
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Quantity:
1 g
5 g
25 g
This item is not returnable. View return policy
5467-74-3
C6H6BBrO2
200.83
MFCD00002104
QBLFZIBJXUQVRF-UHFFFAOYSA-N
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
79599
(4-bromophenyl)boronic acid
OB(O)C1=CC=C(Br)C=C1
This item is not returnable. View return policy
5467-74-3
C6H6BBrO2
200.83
MFCD00002104
QBLFZIBJXUQVRF-UHFFFAOYSA-N
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
79599
(4-bromophenyl)boronic acid
OB(O)C1=CC=C(Br)C=C1

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.

Applications
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.

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
TRUSTED_SUSTAINABILITY
Melting Point 282°C to 286°C
Quantity 1 g
Beilstein 2936347
Solubility Information Soluble in methanol. Insoluble in water.
Formula Weight 200.83
Percent Purity ≥97%
Chemical Name or Material 4-Bromobenzeneboronic acid

RUO – Research Use Only

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