|
| 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 |
|