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4-(Methanesulfonyl)phenylboronic acid

ALDRICH/675903 - ≥95.0%

Synonym: 4-(Methanesulfonyl)benzeneboronic acid; 4-(Methylsulfonyl)phenylboronic acid; 4-Methansulfonylphenylboronic acid

CAS Number: 149104-88-1
Empirical Formula (Hill Notation): C7H9BO4S
Molecular Weight: 200.02
MDL Number: MFCD01630820
Linear Formula: (H3CSO2)C6H4B(OH)2
Product Type: Chemical

Catalog Number PKG Qty. Price Quantity
45-675903-1G 1 g
$44.70
1/EA
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This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material. This image depicts SKU: 675903-1G
This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material. This image depicts SKU: 675903-5G

 

assay ≥95.0%
form solid
InChI 1S/C7H9BO4S/c1-13(11,12)7-4-2-6(3-5-7)8(9)10/h2-5,9-10H,1H3
InChI key VDUKDQTYMWUSAC-UHFFFAOYSA-N
mp 289-293 °C
SMILES string CS(=O)(=O)c1ccc(cc1)B(O)O
Application: 4-(Methanesulfonyl)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


Reagent used in Preparation of
• diarylaminopyridines as potential anti-malarial agents
• hydropyranopyrazine via chloropyrazinecarboxaldehyde and olefination
• biaryl sulfone derivatives as antagonists of the histamine H3 receptor
• novel kinase inhibitor scaffolds with potential antitumor effects
• Hepatitis C virus inhibition activity of N-hydroxyisoquinoline di
Application: Highly effective boronic acid used in a rhodium-catalyzed asymmetric 1,4-addition to 4-oxobutenamides.
General description: Contains varying amounts of anhydride
Packaging: 1, 5 g in glass bottle
RIDADR NONH for all modes of transport
WGK Germany WGK 3
Flash Point(F) Not applicable
Flash Point(C) Not applicable
Purity ≥95.0%
mp 289-293 °C
UNSPSC 12352103

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