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| | 6,7-DIHYDRO-2-PENTAFLUOROPHENYL-5H-PYRROLO(2,1-C)-1,2,4-TRIAZOLIUM TETRAFLUOROBORATE, 97% Basic information | | Reaction |
| Product Name: | 6,7-DIHYDRO-2-PENTAFLUOROPHENYL-5H-PYRROLO(2,1-C)-1,2,4-TRIAZOLIUM TETRAFLUOROBORATE, 97% | | Synonyms: | 6,7-Dihydro-2-pentafluorophenyl-5H-pyrrole[2,1-c]-1,2,4-triazolium tetrafluoroborate, min. 98%;6,7-Dihydro-2-pentafluorophenyl-5H-pyrrolo[2,1-c]-1,2,4-triazoliuM tetrafluoroborat;5H-Pyrrolo[2,1-c]-1,2,4-triazoliuM, 6,7-dihydro-2-(pentafluorophenyl)-, tetrafluoroborate(1-);2-(2,3,4,5,6-pentafluorophenyl)-6,7-dihydro-5H-pyrrolo[2,1-c][1,2,4]triazol-4-ium,tetrafluoroborate;6,7-Dihydro-2-pentafluorophenyl-5H-pyrrolo[2,1-c][1,2,4]triazolium Tetrafluoroborate;2-(Perfluorophenyl)-6,7-dihydro-5H-pyrrolo[2,1-c][1,2,4]triazol-2-ium tetrafluoroborate;6,7-Dihydro-2-(2,3,4,5,6-pentafluorophenyl)-5H-pyrrolo[2,1-c]-1,2,4-triazolium Tetrafluoroborate;6,7-Dihydro-2-pentafluorophenyl-5H-pyrrolo[2,1-c][1,2,4]triazolium Tetrafluoroborate > | | CAS: | 862095-91-8 | | MF: | C11H7BF9N3 | | MW: | 0 | | EINECS: | | | Product Categories: | Achiral Nitrogen;NHC;organic amine salt;Catalysis and Inorganic Chemistry;Chemical Synthesis;NHC Compounds | | Mol File: | 862095-91-8.mol |  |
| | 6,7-DIHYDRO-2-PENTAFLUOROPHENYL-5H-PYRROLO(2,1-C)-1,2,4-TRIAZOLIUM TETRAFLUOROBORATE, 97% Chemical Properties |
| Melting point | 245 °C | | storage temp. | Inert atmosphere,Room Temperature | | form | Powder | | color | tan |
| Hazard Codes | C | | Risk Statements | 34 | | Safety Statements | 26-36/37/39-45 | | RIDADR | UN 1759 8/PG 2 | | WGK Germany | 3 | | HazardClass | 8 | | PackingGroup | II | | HS Code | 2933399990 |
| | 6,7-DIHYDRO-2-PENTAFLUOROPHENYL-5H-PYRROLO(2,1-C)-1,2,4-TRIAZOLIUM TETRAFLUOROBORATE, 97% Usage And Synthesis |
| Reaction |
- Reagent used in the highly enantioand diastereoselective, catalytic intramolecular Stetter reaction.
- Enantioselective synthesis of β-hydroxy and β-amino esters.
- Organocatalytic iminium ion/carbene reaction cascade for the formation of 2,4-disubstituted cyclopentenones.
- Synthesis of alloand epi-Inositol via the NHC-catalyzed carbocyclization of carbohydrate-derived dialdehydes
| | Uses | This triazolium catalyst is used for intermolecular homodimerization of aryl aldehydes, intramolecular aldehyde-ketone benzoin cyclizations, and intramolecular Stetter reations. |
| | 6,7-DIHYDRO-2-PENTAFLUOROPHENYL-5H-PYRROLO(2,1-C)-1,2,4-TRIAZOLIUM TETRAFLUOROBORATE, 97% Preparation Products And Raw materials |
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