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

29.75 EUR - 389.94 EUR

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 acidShow MoreShow Less
PubChem CID 79599
IUPAC Name (4-bromophenyl)boronic acid
SMILES OB(O)C1=CC=C(Br)C=C1
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Products 3
Product Code Brand Quantity Price Quantity & Availability  
Product Code Brand Quantity Price Quantity & Availability  
11301337
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Thermo Scientific Alfa Aesar
L01565.03
1 g
29.75 EUR
1g
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11311337
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Thermo Scientific Alfa Aesar
L01565.06
5 g
95.48 EUR
5g
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11321337
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Thermo Scientific Alfa Aesar
L01565.14
25 g
389.94 EUR
25g
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Description

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.

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
Specifications
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Safety and Handling

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

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missing translation for 'rtecsNumber' : CY8650000

missing translation for 'tsca' : No

Recommended Storage : Ambient temperatures

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Product Certifications

RUO – Research Use Only

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