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| 2,4,6-Trifluorophenylboronic acid Basic information |
Product Name: | 2,4,6-Trifluorophenylboronic acid | Synonyms: | 2,4,6-TRIFLUOROPHENYLBORONIC ACID;RARECHEM AH PB 0121;2,4,6-Trifluoronenzeneboronic acid;2,4,6-Trifluorophenylboronic;2,4,6-TRIFLUOROBENZENEBORONIC ACID;2,4,6-Trifluorophenylboronic Acid (contains varying aMounts of Anhydride);Trifluorobenzeneboronic aci;2,4,6-trifluorophenyl(dihydroxy)borane | CAS: | 182482-25-3 | MF: | C6H4BF3O2 | MW: | 175.9 | EINECS: | 681-558-8 | Product Categories: | FluoroCompounds;Heterocyclic Compounds;Boronic Acid;Aryl;Organoborons;Boronic Acids;Boronic Acids and Derivatives;blocks;BoronicAcids | Mol File: | 182482-25-3.mol | |
| 2,4,6-Trifluorophenylboronic acid Chemical Properties |
Melting point | 228-235 °C (lit.) | Boiling point | 236.0±50.0 °C(Predicted) | density | 1.44±0.1 g/cm3(Predicted) | storage temp. | Inert atmosphere,Store in freezer, under -20°C | solubility | soluble in Methanol | pka | 8.26±0.58(Predicted) | form | Crystalline Powder | color | White to off-white | BRN | 8549766 | CAS DataBase Reference | 182482-25-3(CAS DataBase Reference) |
| 2,4,6-Trifluorophenylboronic acid Usage And Synthesis |
Chemical Properties | Off-white Cryst | Uses | Reactant involved in:
- Synthesis of phenylboronic catechol esters
- Suzuki-Miyaura coupling reactions with aryl chlorides and unstable polyfluorophenyl
- Enantioselective borane reduction of trifluoroacetophenone
- Transmetalation
| Uses | suzuki reaction |
| 2,4,6-Trifluorophenylboronic acid Preparation Products And Raw materials |
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