4-(Methylsulfonyl)phenylboronic Acid CAS 149104-88-1 Purity >99.5% (HPLC)

Short Description:

Chemical Name: 4-(Methylsulfonyl)phenylboronic Acid

CAS: 149104-88-1

Purity: >99.5% (HPLC)

Appearance: White to Off-White Powder

High Quality, Commercial Production

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Product Detail

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Description:

Manufacturer Supply With High Quality, Commercial Production
Chemical Name: 4-(Methylsulfonyl)phenylboronic Acid
CAS: 149104-88-1

Chemical Properties:

Chemical Name	4-(Methylsulfonyl)phenylboronic Acid
Synonyms	4-(Methanesulfonyl)phenylboronic Acid; 4-(Methanesulfonyl)benzeneboronic Acid
CAS Number	149104-88-1
CAT Number	RF-PI1284
Stock Status	In Stock, Production Scale Up to 25 Tons/Month
Molecular Formula	C7H9BO4S
Molecular Weight	200.02
Melting Point	275.0~277.0℃
Solubility	Soluble in Methanol
Brand	Ruifu Chemical

Specifications:

Item	Specifications
Appearance	White to Off-White Powder
Purity / Analysis Method	>99.5% (HPLC)
Purity / Analysis Method	98.0~102.0% (Titration by NaOH)
Loss on Drying	<0.50%
Single Impurity	<0.50%
Heavy Metals (as Pb)	<20ppm
Infrared Spectrum	Conforms to Structure
Proton NMR Spectrum	Conforms to Structure
Test Standard	Enterprise Standard
Usage	Pharmaceutical 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:

FAQ:

Application:

4-(Methylsulfonyl)phenylboronic Acid (CAS: 149104-88-1) is a derivative of boric acid and the downstream products are very rich. 4-(Methylsulfonyl)phenylboronic Acid may be used as reagent for: sequential Suzuki cross-coupling reactions; Copper-catalyzed oxidative trifluoromethylthiolation of aryl boronic acids; directed metalation and regioselective functionalization of 3-bromofuran and related heterocycles; Barton-Zard pyrrole cyclocondensations and Baeyer-Villiger oxidations; diplar cycloaddition and palladium-catalyzed cross-coupling processes; continuous flow Suzuki reactions for odanacatib intermediate synthesis.