3,4,5-Trifluorophenylboronic acid

3,4,5-Trifluorophenylboronic acid Basic information
Uses
Product Name:3,4,5-Trifluorophenylboronic acid
Synonyms:AKOS BRN-0138;3,4,5-TRIFLUOROPHENYLBORONIC ACID;3,4,5-TRIFLUOROBENZENEBORONIC ACID;3,4,5-Trifluorobenzeneboronic acid 97%;3,4,5-Trifluorobenzeneboronicacid97%;3,4,5-TRIFLUOROPHENYLBORONIC ACID MIN 96% HPLC;3,4,5-Trifluorophenylboronic Aicd;Boronic acid, B-(3,4,5-trifluorophenyl)-
CAS:143418-49-9
MF:C6H4BF3O2
MW:175.9
EINECS:604-355-8
Product Categories:Piperidines;Boronic Acids;Boronic Acids;Boronic Acids and Derivatives;Aryl;Fluorinated;Organoborons;Substituted Boronic Acids;Fluorin-contained phenyl boronic acid series;Boronic Acid;blocks;BoronicAcids;Boronic Acid series;Fluoro-Aromatics
Mol File:143418-49-9.mol
3,4,5-Trifluorophenylboronic acid Structure
3,4,5-Trifluorophenylboronic acid Chemical Properties
Melting point 290-295 °C (lit.)
Boiling point 263.6±50.0 °C(Predicted)
density 1,087g/cm
refractive index 1,423-1,425
storage temp. Keep in dark place,Sealed in dry,Room Temperature
solubility 18.43g/l
pka6.54±0.11(Predicted)
form Powder
color Tan
BRN 7371914
InChIKeyUHDDEIOYXFXNNJ-UHFFFAOYSA-N
CAS DataBase Reference143418-49-9(CAS DataBase Reference)
Safety Information
Hazard Codes N-Xn,Xi
Risk Statements 51/53-36-22-36/37/38
Safety Statements 61-26-37/39-36
RIDADR 3077
WGK Germany 3
HazardClass IRRITANT
HS Code 29163990
MSDS Information
ProviderLanguage
ACROS English
SigmaAldrich English
ALFA English
3,4,5-Trifluorophenylboronic acid Usage And Synthesis
UsesReactant involved in:
• Preparation of phenylboronic catechol esters and determination of Lewis acidity
• Synthesis of benzopyranone derivatives as GABAA receptor modulators
• Synthesis of multisubstituted olefins and conjugate dienes
• Suzuki cross-coupling reactions
• Preparation of fluorinated aromatic poly(ether-amide)s




Chemical PropertiesTan powder
UsesIntermediates of Liquid Crystals
UsesReactant involved in:
  • Preparation of phenylboronic catechol esters and determination of Lewis acidity
  • Synthesis of benzopyranone derivatives as GABAA receptor modulators
  • Synthesis of multisubstituted olefins and conjugate dienes
  • Suzuki cross-coupling reactions
  • Preparation of fluorinated aromatic poly(ether-amide)s
Usessuzuki reaction
3,4,5-Trifluorophenylboronic acid Preparation Products And Raw materials
Preparation Products3',4',5'-trifluorobiphenyl-2-aMine-->3,4,5-TRIFLUOROBENZOTRIFLUORIDE-->4-Bromo-2,3',4',5'-tetrafluorobiphenyl-->3',4',5'-Trifluorobiphenyl-4-ol
3,4,5-TRIFLUOROPHENYLBORONIC ACID, PINACOL ESTER 3,5-Difluorophenylboronic acid 2,3,6-Trifluorophenylboronic acid 2,3,4-Trifluorophenylboronic Acid (contains varying amounts of Anhydride),4-TRIFLUOROPHENYLBORONIC ACID,2,3,4-TRIFLUOROPHENYLBORONIC ACID 5-Bromo-2,3,4-Trifluorophenylboronic acid 2,3,6-TRIFLUOROPHENYLBORONIC ACID 2-TRIFLUOROPHENYLBORONIC ACID 3-BUTOXY-2,4,6-TRIFLUOROPHENYLBORONIC ACID 3-ETHOXY-2,4,6-TRIFLUOROPHENYLBORONIC ACID 3-ISOPROPOXY-2,4,6-TRIFLUOROPHENYLBORONIC ACID 3-METHOXY-2,4,6-TRIFLUOROPHENYLBORONIC ACID Phenylboronic acid 2,4,5-Trifluorophenylboronic acid 3-(4-Carboxybutoxy)-2,4,6-trifluorophenylboronic acid 6-Bromo-2,3,4-Trifluorophenylboronic acid 3-(tert-Butyldimethylsilyloxy)-2,4,6-trifluorophenylboronic acid 2-AMINO-3,4,5-TRIFLUOROPHENYLBORONIC ACID 3-PROPOXY-2,4,6-TRIFLUOROPHENYLBORONIC ACID

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