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ChemicalBook >  Product Catalog >  Organic Chemistry >  Organic fluorine compound >  Fluorophenyl boronic acid series >  2,3,4,5,6-PENTAFLUOROBENZENEBORONIC ACID

2,3,4,5,6-PENTAFLUOROBENZENEBORONIC ACID

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2,3,4,5,6-PENTAFLUOROBENZENEBORONIC ACID Basic information

Product Name:
2,3,4,5,6-PENTAFLUOROBENZENEBORONIC ACID
Synonyms:
  • Perfluorophenylboronic acid
  • Te5152
  • PERFLUOROPHENYLBORONIC ACID;RARECHEM AH PB 0049;
  • Perfluorobenzeneboronic acid
  • 2,3,4,5,6-Pentafluorobenzeneboronic acid (Free of Anhydride)
  • RARECHEM AH PB 0049
  • PENTAFLUOROPHENYLBORONIC ACID
  • PENTAFLUOROBENZENEBORONIC ACID
CAS:
1582-24-7
MF:
C6H2BF5O2
MW:
211.88
EINECS:
627-867-3
Product Categories:
  • Aryl
  • Boronic Acids
  • blocks
  • BoronicAcids
  • Heterocyclic Compounds
  • Boronic Acids and Derivatives
Mol File:
1582-24-7.mol
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2,3,4,5,6-PENTAFLUOROBENZENEBORONIC ACID Chemical Properties

Melting point:
176-179°C
Boiling point:
244.0±50.0 °C(Predicted)
Density 
1.61±0.1 g/cm3(Predicted)
storage temp. 
Inert atmosphere,Store in freezer, under -20°C
solubility 
Miscible with alcohols, acetonitrile and dichloromethane.
pka
6.13±0.58(Predicted)
form 
powder
color 
White to Almost white
Sensitive 
Moisture Sensitive
BRN 
3033960
InChI
InChI=1S/C6H2BF5O2/c8-2-1(7(13)14)3(9)5(11)6(12)4(2)10/h13-14H
InChIKey
VASOMTXTRMYSKD-UHFFFAOYSA-N
SMILES
B(C1=C(F)C(F)=C(F)C(F)=C1F)(O)O
CAS DataBase Reference
1582-24-7(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36/37/39-36
WGK Germany 
3
HazardClass 
IRRITANT
HS Code 
29319090

MSDS

  • Language:English Provider:ALFA
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2,3,4,5,6-PENTAFLUOROBENZENEBORONIC ACID Usage And Synthesis

Chemical Properties

White solid

Uses

2,3,4,5,6-Pentafluorobenzeneboronic acid is utilized in the palladium-catalyzed Suzuki reaction to synthesize several cross-coupled aromatic compounds, for example bis(pentafluorophenyl)-substituted thiophene and selenophene derivatives. It serves as an intermediate and raw material in pharmaceutical and chemical industry. It is also used in dyes and pigments. It can be used to prepare cyclic boronates of bifunctional compounds.

Uses

Reactant for:

  • Preparation of phenylboronic catechol esters as promising anion receptors for polymer electrolytes
  • Preparation of biaryls via palladium-catalyzed homocoupling reaction
  • Prepartion of quaternary a,a-heterodiaryl carboxylic esters via rhodium-catalyzed cross-coupling
  • C-C cross-coupling reactions

2,3,4,5,6-PENTAFLUOROBENZENEBORONIC ACIDSupplier

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