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3,5-Bis(trifluoromethyl)benzeneboronic acid

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3,5-Bis(trifluoromethyl)benzeneboronic acid Basic information

Product Name:
3,5-Bis(trifluoromethyl)benzeneboronic acid
Synonyms:
  • RARECHEM AH PB 0029
  • 3,5-Bis(trifluoromethyl)benzeneboronic acid, 97+%
  • 3,5-Bis(trifluoromethyl)phenylboranic acid
  • Boric acid 3,5-bis(trifluoromethyl)phenyl ester
  • 3,5-Bis(trifluoromethyl)benzeneboronic acid,95%
  • 3,4-Bis(trifluoromethyl) phenylboronic acid
  • 5-Bis(trifluoroMethyl)phenylboronic acid
  • 3,5-Bis(trifloroMethyl)phenylboronic acid
CAS:
73852-19-4
MF:
C8H5BF6O2
MW:
257.93
EINECS:
642-864-7
Product Categories:
  • Substituted Boronic Acids
  • blocks
  • BoronicAcids
  • FluoroCompounds
  • Boric Acid
  • Boronic Acid series
  • Fluorides
  • Fluorin-contained phenyl boronic acid series
  • Boronic Acid
  • Aryl
  • B (Classes of Boron Compounds)
  • Boronic Acids
  • Boronic Acids
  • Boronic Acids and Derivatives
  • Organoborons
  • Trifluoromethyl
  • Boronate Ester
  • Potassium Trifluoroborate
Mol File:
73852-19-4.mol
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3,5-Bis(trifluoromethyl)benzeneboronic acid Chemical Properties

Melting point:
217-220 °C (lit.)
Boiling point:
248.1±50.0 °C(Predicted)
Density 
1.50±0.1 g/cm3(Predicted)
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
solubility 
soluble in Methanol
form 
Crystals or Powder
pka
6.57±0.10(Predicted)
color 
White to light yellow
BRN 
7379990
InChIKey
BPTABBGLHGBJQR-UHFFFAOYSA-N
CAS DataBase Reference
73852-19-4(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
37/39-26
WGK Germany 
3
TSCA 
No
HazardClass 
IRRITANT
HS Code 
29163990

MSDS

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3,5-Bis(trifluoromethyl)benzeneboronic acid Usage And Synthesis

Chemical Properties

Off-white Cryst

Uses

suzuki reaction

Uses

Reactant involved in the synthesis of:

  • Methylene-arylbutenones via carbonylative arylation of allenols
  • 4-aminoquinoline analogs via Ullman / Suzuki / Negishi coupling
  • Primary amino acid derivatives with anticonvulsant activity
  • Alkyl arylcarbamates via Cu-catalyzed coupling with potassium cyanate
  • Aryl-substituted succinimides and cyclic ketones by asymmetric conjugate addition
  • Axially chiral dicarboxylic acids for asymmetric Mannich-type reactions

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