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
  • CAS No.:195062-61-4
Other grades of this product :
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
EINECS:
Product Categories:Chemical Synthesis;Organometallic Reagents;Aryl Boronate Esters;Boronate Esters;Boronic Acids and Derivatives
Mol File:195062-61-4.mol
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)
Fp >230 °F
storage temp. 2-8°C
solubility soluble in Methanol
form Solid
color White to pale brown
InChIKeyNYARTXMDWRAVIX-UHFFFAOYSA-N
CAS DataBase Reference195062-61-4
Safety Information
Hazard Codes Xn
Risk Statements 22
Safety Statements 36
WGK Germany 3
HS Code 2931900090
MSDS Information
ProviderLanguage
SigmaAldrich English
4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)CHLOROBENZENE Usage And Synthesis
Uses4-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.

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