4-Chlorophenylboronic Acid CAS 1679-18-1 Purity >99.5% (HPLC) Factory High Quality

Chemical Name: 4-Chlorophenylboronic Acid  CAS: 1679-18-1 Purity: >99.5% (HPLC) Appearance: White 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-Chlorophenylboronic Acid CAS: 1679-18-1
Item Specifications
Appearance White to Off-White Powder
Purity / Analysis Method >99.5% (HPLC)
Melting Point 284.0~289.0℃
Moisture (K.F) <0.50%
Residue on Ignition <0.20%
Single Impurity <0.50%
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-Chlorophenylboronic Acid
Synonyms 4-Chlorobenzeneboronic Acid; p-Chlorophenylboronic Acid
CAS Number 1679-18-1
CAT Number RF-PI1315
Stock Status In Stock, Production Scale Up to 25 Tons/Month
Molecular Formula C6H6BClO2
Molecular Weight 156.37 
Solubility Soluble in Methanol; Slightly Soluble in Water
Brand Ruifu Chemical

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Application:

4-Chlorophenylboronic Acid (CAS: 1679-18-1), can be used as pharmaceutical and material intermediates. It is also an important intermediate for the OLED production, widely used in electronic materials. 4-Chlorophenylboronic Acid can be used as a reactant in: Suzuki-Miyaura Cross Coupling Reaction; Palladium-catalyzed direct arylation; Cyclopalladation; Tandem-type Pd(II)-catalyzed oxidative Heck reaction and intramolecular C-H amidation; Copper-mediated ligandless aerobic fluoroalkylation; Pd-catalyzed arylative cyclization. Ruthenium catalyzed direct arylation; Ligand-free copper-catalyzed coupling reactions; Regioselective arylation and alkynylation by Suzuki-Miyaura and Sonogashira cross-coupling reactions. It can also be used to prepare: Substituted diarylmethylidenefluorenes via Suzuki coupling reaction; Baclofen lactam by Suzuki coupling of a pyrrolinyl tosylate, followed by hydrogenation reaction; Palladium(II) thiocarboxamide complexes as Suzuki coupling catalysts.

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