3-Chlorophenylboronic Acid CAS 63503-60-6 Purity >99.5% (HPLC) Factory High Quality

Short Description:

Chemical Name: 3-Chlorophenylboronic Acid 

CAS: 63503-60-6

Purity: >99.5% (HPLC)

Appearance: White Powder

High Quality, Commercial Production

E-Mail: alvin@ruifuchem.com


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Description:

Manufacturer Supply With High Quality, Commercial Production 
Chemical Name: 3-Chlorophenylboronic Acid CAS: 63503-60-6

Chemical Properties:

Chemical Name 3-Chlorophenylboronic Acid
Synonyms 3-Chlorobenzeneboronic Acid; m-Chlorophenylboronic Acid; m-Chlorobenzeneboronic Acid
CAS Number 63503-60-6
CAT Number RF-PI1320
Stock Status In Stock, Production Scale Up to 25 Tons/Month
Molecular Formula C6H6BClO2
Molecular Weight 156.37
Melting Point 185.0-189.0℃ (lit.) 
Solubility Soluble in Methanol, Ether, Tetrahydrofuran; Slightly Soluble in Water
Brand Ruifu Chemical

Specifications:

Item Specifications
Appearance White Powder
Purity / Analysis Method >99.5% (HPLC)
Loss on Drying <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

Package & Storage:

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.

Advantages:

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FAQ:

Application:

3-Chlorophenylboronic Acid (CAS: 63503-60-6) is used as pharmaceutical intermediates, OLED intermediates, liquid crystal intermediates, display material. Shanghai Ruifu Chemical Co., Ltd. is the leading manufacturer and supplier of 3-Chlorophenylboronic Acid with high quality. 3-Chlorophenylboronic Acid is employed as a reactant involved in 1,4-conjugate addition reactions with ethenesulfonamides to form arylethanesulfonamides, Suzuki-Miyaura reactions with dibromotrifluoromethylbenzene, cross-coupling reactions with diazoesters or potassium cyanate. It is involved in the synthesis of biarylketones and phthalides and synthesis of inhibitors including PDE4 inhibitors6 among others.

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