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ChemicalBook >  Product Catalog >  Chemical Reagents >  Organic reagents >  Borane >  4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)CHLOROBENZENE

4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)CHLOROBENZENE

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4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)CHLOROBENZENE Basic information

Product Name:
4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)CHLOROBENZENE
Synonyms:
  • 2-(4-Chlorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
  • 4-Chlorobenzeneboronic acid, pinacol ester
  • 4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)CHLOROBENZENE
  • 4-CHLOROPHENYLBORONIC ACID, PINACOL ESTER
  • 4-Chlorophenylboronic acid pinacol ester 97%
  • Pinacol (4-chlorophenyl)boronate
  • Pinac
  • 1,3,2-Dioxaborolane, 2-(4-chlorophenyl)-4,4,5,5-tetramethyl-
CAS:
195062-61-4
MF:
C12H16BClO2
MW:
238.52
Product Categories:
  • Chemical Synthesis
  • Organometallic Reagents
  • Aryl Boronate Esters
  • Boronate Esters
  • Boronic Acids and Derivatives
Mol File:
195062-61-4.mol
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4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)CHLOROBENZENE Chemical Properties

Melting point:
50-55 °C(lit.)
Boiling point:
308.7±25.0 °C(Predicted)
Density 
1.10±0.1 g/cm3(Predicted)
Flash point:
>230 °F
storage temp. 
2-8°C
solubility 
soluble in Methanol
form 
Solid
color 
White to pale brown
InChIKey
NYARTXMDWRAVIX-UHFFFAOYSA-N
CAS DataBase Reference
195062-61-4
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Safety Information

Hazard Codes 
Xn
Risk Statements 
22
Safety Statements 
36
WGK Germany 
3
HS Code 
2931900090

MSDS

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4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)CHLOROBENZENE Usage And Synthesis

Uses

4-Chlorophenylboronic acid pinacol ester can be used as a reagent in Suzuki-Miyaura cross-coupling reaction to form C-C bonds by reacting with different aryl halides over palladium catalysts.
It can also be used as a reactant:

  • To prepare 2-(4-chlorophenyl)-4H-chromen-4-one by treating with 4-chromanone via one-pot palladium-catalyzed dehydrogenation and oxidative boron-Heck coupling reaction.
  • In the ligand-enabled C-H bond activation reaction in the presence of a palladium catalyst.
  • To synthesize biaryl amides via Cu-catalyzed C-H bond coupling of aryl arylamides.

4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)CHLOROBENZENESupplier

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