| Identification | More | [Name]
1-FLUORO-2,6-DICHLOROPYRIDINIUM TRIFLATE | [CAS]
130433-68-0 | [Synonyms]
F-PLUS T800 (FP-T800)
2,6-dichloro-1-fluoropyridin-1-ium
N-FLUORO-2,6-DICHLOROPYRIDINIUM TRIFLATE
1-FLUORO-2,6-DICHLOROPYRIDINIUM TRIFLATE
2,6-DICHLORO-1-FLUOROPYRIDINIUM TRIFLATE
N-Fluoro-2,6-dichloropyridiniumtriflate97%
N-Fluoro-2,6-dichloropyridinium triflate 97%
2,6-Dichloro-1-fluoropyridinium triflate 95%
1-FLUORO-2,6-DICHLOROPYRIDINIUM TRIFLATE 94+%
2,6-DICHLORO-1-FLUOROPYRIDINIUM TRIFLUOROMETHANESULFONATE
2,6-Dichloro-1-fluoropyridin-1-iuM trifluoroMethanesulfonate
2,6-Dichloro-1-fluoropyridinium triflate ISO 9001：2015 REACH
1-Fluoro-2,6-dichloropyridinium Triflate [Fluorinating Reagent]
2,6-Dichloro-1-fluoropyridinium Trifluoromethanesulfonate [Fluorinating Reagent]
2,6-Dichloro-1-fluoropyridinium Triflate
1-Fluoro-2,6-dichloropyridinium Triflate | [Molecular Formula]
C6H3Cl2F4NO3S | [MDL Number]
MFCD00191438 | [Molecular Weight]
316.06 | [MOL File]
130433-68-0.mol |
| Safety Data | Back Directory | [Hazard Codes ]
C,Xi | [Risk Statements ]
R34:Causes burns. | [Safety Statements ]
S45:In case of accident or if you feel unwell, seek medical advice immediately (show label where possible) .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice . | [RIDADR ]
UN 3261 8 / PGII | [WGK Germany ]
3 | [Hazard Note ]
Irritant | [TSCA ]
No | [HazardClass ]
IRRITANT | [HS Code ]
29333999 |
| Hazard Information | Back Directory | [Chemical Properties]
yellow powder | [Uses]
- Used in the fluorination of various organic compounds
- Fluoropyridinium triflates are versatile reagents for transformation of thioglycosides into ο-glycoside, glycosyl azide and sulfoxide
- Electrolytic partial fluorination and diastereoselective anodic fluorination
- Regioselective, electrochemical fluorination
- Fluorination of alkenes with N-F type of reagents
| [Uses]
2,6-Dichloro-1-fluoropyridinium triflate can be used in the fluorination of various organic compounds.
| [Uses]
N-fluoropyridinium triflate salts offer a tunable fluorinating system; electronic nature of the substituents on the ring dictates the potency and selectivity of the reagent. Efficient fluorination of various aromatics, carbanions, vinyl esters, alkyls, and enamines. |
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