4-Bromophenylboronic Acid CAS 5467-74-3 Purity >99.5% (HPLC) Factory High Quality

Chemical Name: 4-Bromophenylboronic Acid  CAS: 5467-74-3 Purity: >99.5% (HPLC) Appearance: White to Off-White Crystal Powder High Quality, Commercial Production E-Mail: alvin@ruifuchem.com

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Chemical Properties:

Package: Bottle, Aluminium foil bag, 25kg/Cardboard Drum, or according to customer's requirement. Storage Condition: Store in sealed containers at cool and dry place; Protect from light and moisture.Manufacturer Supply With High Quality, Commercial Production  Chemical Name: 4-Bromophenylboronic Acid CAS: 5467-74-3
Item Specifications
Appearance White to Off-White Crystal Powder
Purity / Analysis Method >99.5% (HPLC)
Melting Point 284.0~288.0℃
Specific Gravity (25/25℃) 0.866~0.869
Loss on Drying <0.50%
Single Impurity <0.30%
Total Impurities <0.50%
Heavy Metals (as Pb) <20ppm
Test Standard Enterprise Standard
Usage Pharmaceutical Intermediates; OLED Intermediates

Description:

Specifications:

Package & Storage:

Chemical Name 4-Bromophenylboronic Acid
Synonyms 4-Bromobenzeneboronic Acid
CAS Number 5467-74-3
CAT Number RF-PI1273
Stock Status In Stock, Production Scale Up to 25 Tons/Month
Molecular Formula C6H6BBrO2
Molecular Weight 200.83
Solubility Soluble in Methanol; Insoluble in Water
Brand Ruifu Chemical

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Application:

4-Bromophenylboronic Acid (CAS: 5467-74-3) is mainly used as organic synthesis intermediates, pharmaceutical intermediates and OLED intermediates, liquid crystal intermediates or display materials. 4-Bromophenylboronic 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.

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