4-Bromophenylboronic Acid CAS 5467-74-3 In Stock With Good Quality And Price

4-Bromophenylboric acid CAS:5467-74-3 is used as reagent in various important catalytic reaction which includes: a).Palladium catalyzed Suzuki-Miyaura cross-couplings; b). Pd(II)-catalyzed diastereoselective conjugate additions; c). Palladium-catalyzed stereoselective Heck-type reaction of allylic esters with arylboronic acids; d).Tandem-type Pd(II)-catalyzed oxidative Heck reaction and intramolecular C-H amidation sequence; e). Copper-mediated ligandless aerobic fluoroalkylation of arylboronic acids with fluoroalkyl iodides; d). Pd-catalyzed arylative cyclization of alkyne-tethered enals or enones via carbopalladation of alkynes; e). Copper-catalyzed cross-couplings. 4-Bromophenylboric acid CAS:5467-74-3 is also used in Preparation of a). Gallate-based obovatol analogs with potential anti-tumor activity and b). Protein modulators and enzymatic and kinase inhibitors. 4-Bromophenylboric acid is used in the preparation of arylboronates as inhibitors of fatty acid amide hydrolase.
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Product Details

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Product Description

Name

4-Bromophenylboronic acid CAS 5467-74-3 in stock with good quality

Other name

(4-Bromophenyl)boronic acid ; 4-Bromobenzeneboronic acid

CAS

5467-74-3

Applications

Organic intermediate 

Appearance

off-white powder

4-Bromophenylboric acid CAS:5467-74-3 is used as reagent in various important catalytic reaction which includes: a).Palladium catalyzed Suzuki-Miyaura cross-couplings; b). Pd(II)-catalyzed diastereoselective conjugate additions; c). Palladium-catalyzed stereoselective Heck-type reaction of allylic esters with arylboronic acids; d).Tandem-type Pd(II)-catalyzed oxidative Heck reaction and intramolecular C-H amidation sequence; e). Copper-mediated ligandless aerobic fluoroalkylation of arylboronic acids with fluoroalkyl iodides; d). Pd-catalyzed arylative cyclization of alkyne-tethered enals or enones via carbopalladation of alkynes; e). Copper-catalyzed cross-couplings.
4-Bromophenylboric acid is also used in Preparation of a). Gallate-based obovatol analogs with potential anti-tumor activity and b). Protein modulators and enzymatic and kinase inhibitors.
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