Basic information Safety Supplier Related

4-(TERT-BUTYLDIMETHYLSILYLOXY)PHENYLBORONIC ACID

Basic information Safety Supplier Related

4-(TERT-BUTYLDIMETHYLSILYLOXY)PHENYLBORONIC ACID Basic information

Product Name:
4-(TERT-BUTYLDIMETHYLSILYLOXY)PHENYLBORONIC ACID
Synonyms:
  • oxy)phenyL
  • 4-(T-BUTYL DIMETHYLSILOXY) PHENYL BORONIC ACID
  • 4-(TERT-BUTYL DIMETHYLSILOXY)PHENYL BORONIC ACID
  • 4-(TERT-BUTYLDIMETHYLSILYLOXY)PHENYLBORONIC ACID
  • 4-(TERT-BUTYLDIMETHYLSILYOXY)PHENYLBORONIC ACID
  • AKOS BRN-0412
  • 4-(TERT-BUTYLDIMETHYLSILYOXY)PHENYLBORON
  • 4-(tert-Butyldimethylsilyloxy)benzeneboronic acid
CAS:
159191-56-7
MF:
C12H21BO3Si
MW:
252.19
Product Categories:
  • blocks
  • BoronicAcids
  • Aryl
  • Organoborons
  • Boronic acid
  • Boronic Acids
  • Boronic Acids
  • Boronic Acids and Derivatives
  • Aryl Boronic Acids
  • Boronic Acids and Derivatives
  • Chemical Synthesis
  • Monosubstituted Aryl Boronic Acids
  • Organometallic Reagents
Mol File:
159191-56-7.mol
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4-(TERT-BUTYLDIMETHYLSILYLOXY)PHENYLBORONIC ACID Chemical Properties

Melting point:
194-198 °C (lit.)
Boiling point:
321.4±44.0 °C(Predicted)
Density 
1.01±0.1 g/cm3(Predicted)
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
form 
powder to crystal
pka
8.68±0.16(Predicted)
color 
White to Almost white
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Safety Information

Hazard Codes 
Xi
WGK Germany 
3
HS Code 
2931900090

MSDS

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4-(TERT-BUTYLDIMETHYLSILYLOXY)PHENYLBORONIC ACID Usage And Synthesis

Uses

Reactant involved in:• ;Asymmetric addition reactions with β-substituted cyclic enones1• ;Hydroarylation and heterocyclization with phenylpropiolates2• ;Double Suzuki-Miyaura coupling reactions3Starting material for the synthesis of red electroluminescent polyfluorenes4Reactant involved in the synthesis of biologically active molecules including:• ;Phenylpyridone derivatives as MCH1R antagonists5• ;Atromentin and its O-alkylated derivatives3• ;Gelatinases and MT1-MMP inhibitors6

Uses

Reactant involved in:

  • Asymmetric addition reactions with β-substituted cyclic enones
  • Hydroarylation and heterocyclization with phenylpropiolates
  • Double Suzuki-Miyaura coupling reactions

Starting material for the synthesis of red electroluminescent polyfluorenes

Reactant involved in the synthesis of biologically active molecules including:
  • Phenylpyridone derivatives as MCH1R antagonists
  • Atromentin and its O-alkylated derivatives
  • Gelatinases and MT1-MMP inhibitors

4-(TERT-BUTYLDIMETHYLSILYLOXY)PHENYLBORONIC ACIDSupplier

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