ChemicalBook Product Catalog Chemical Reagents Organic reagents Boric acid 3,5-Bis(trifluoromethyl)benzeneboronic acid

3,5-Bis(trifluoromethyl)benzeneboronic acid

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 Acids;Boronic Acids and Derivatives;Boronic Acid;B (Classes of Boron Compounds);Boronic Acids;Aryl;Organoborons;Trifluoromethyl;Boronate Ester;Potassium Trifluoroborate
Mol File:73852-19-4.mol
3,5-Bis(trifluoromethyl)benzeneboronic acid Structure
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
pka6.57±0.10(Predicted)
form Crystals or Powder
color White to light yellow
BRN 7379990
InChIKeyBPTABBGLHGBJQR-UHFFFAOYSA-N
CAS DataBase Reference73852-19-4(CAS DataBase Reference)
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 Information
ProviderLanguage
ACROS English
SigmaAldrich English
ALFA English
3,5-Bis(trifluoromethyl)benzeneboronic acid Usage And Synthesis
Chemical PropertiesOff-white Cryst
UsesReactant 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
Usessuzuki reaction
3,5-Bis(trifluoromethyl)benzeneboronic acid Preparation Products And Raw materials
Preparation Products3,5-Bis(trifluoromethyl)phenol
2,5-BIS(TRIFLUOROMETHYL)BENZENEBORONIC ACID,2,5-BIS(TRIFLUOROMETHYL)-BENZENEBORONIC ACID, 97+% 3,4-Bis(trifluoroMethyl)phenylboronic acid 2,5-Bis-Thiopheneboronic acid pinacol ester 2,4-Bis(trifluoromethyl)benzeneboronic acid pinacol ester 2,4-Bis(trifluoromethyl)benzeneboronic acid 98%,2,4-BIS(TRIFLUOROMETHYL)BENZENEBORONIC ACID,2,4-Bis(trifluoromethyl)benzeneboronic acid, 97+% 3-(TRIFLUOROMETHYL)-5-METHYL-PHENYLBORONIC ACID 3-Difluoromethyl-phenylboronic acid ((4S,5S)-(-)-O-[1-BENZYL-1-(5-METHYL-2-PHENYL-4,5-DIHYDROOXAZOL-4-YL)-2-PHENYLETHYL]-DICYCLOHEXYL-PHOSPHINITE)(1,5-COD)IRIDIUM (I) TETRAKIS(3,5-BIS(TRIFLUOROMETHYL)PHENYLBORATE 3-Tolylboronic acid Methylboronic acid METHYL FLUORIDE 1,3-Bis(trifluoromethyl)-benzene Phenylboronic acid 3-(Trifluoromethyl)phenylboronic acid 3,5-Bis(trifluoromethyl)benzeneboronic acid 3,5-Dimethylphenylboronic acid 2,6-BIS(TRIFLUOROMETHYL)BENZENEBORONIC ACID
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