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4-(METHYLSULFONYL)PHENYLBORONIC ACID

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4-(METHYLSULFONYL)PHENYLBORONIC ACID Basic information

Product Name:
4-(METHYLSULFONYL)PHENYLBORONIC ACID
Synonyms:
  • (4-methanesulfonylphenyl)boranediol
  • 4-(Methylsulfonyl)phenylboronic acid ,98%
  • 4-methylfulfonylphenylboronic acid
  • 4-[(Dioxo-lambda~6~-sulfanyl)methyl]phenylboronic acid
  • 4-Boronophenyl methyl sulphone~4-(Methylsulphonyl)phenylboronic acid
  • 4-(methylsulfonyloxy)phenylboronic acid
  • 4-(Methylsulphonyl)benzeneboronic acid
  • 4-Boronophenylmethylsulfone
CAS:
149104-88-1
MF:
C7H9BO4S
MW:
200.02
EINECS:
677-559-8
Product Categories:
  • Boronate Ester
  • Potassium Trifluoroborate
  • Aryl
  • B (Classes of Boron Compounds)
  • Boronic Acids & Esters
  • Phenyls & Phenyl-Het
  • blocks
  • BoronicAcids
  • Boronic Acids & Esters
  • Phenyls & Phenyl-Het
  • Boronic acids
  • Boronic Acid
  • Organoborons
  • Sulfonyl
Mol File:
149104-88-1.mol
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4-(METHYLSULFONYL)PHENYLBORONIC ACID Chemical Properties

Melting point:
275-277 °C
Boiling point:
445.5±51.0 °C(Predicted)
Density 
1.39±0.1 g/cm3(Predicted)
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
solubility 
soluble in Methanol
pka
7.22±0.10(Predicted)
form 
Powder
color 
Off-white
CAS DataBase Reference
149104-88-1(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
37/39-26-24/25-22
WGK Germany 
3
HazardClass 
IRRITANT
HS Code 
29163990

MSDS

  • Language:English Provider:ACROS
  • Language:English Provider:ALFA
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4-(METHYLSULFONYL)PHENYLBORONIC ACID Usage And Synthesis

Chemical Properties

Off-white powder

Uses

4-(Methylsulfonyl)phenylboronic Acid is a heteroaryl boronic acid that was tested for their in vitro hormone-sensitive lipase inhibitory properties.

Uses

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

General Description

Contains varying amounts of anhydride

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