Bis(trifluoromethanesulfonyl)aniline
Appearance
![]() | |
Names | |
---|---|
Preferred IUPAC name
1,1,1-Trifluoro-N-phenyl-N-(trifluoromethanesulfonyl)methanesulfonamide | |
Other names
Phenyl triflimide
| |
Identifiers | |
3D model (JSmol)
|
|
1269141 | |
ChemSpider | |
ECHA InfoCard | 100.116.996 |
EC Number |
|
PubChem CID
|
|
UNII | |
CompTox Dashboard (EPA)
|
|
| |
| |
Properties | |
C8H5F6NO4S2 | |
Molar mass | 357.24 g·mol−1 |
Appearance | White solid |
Melting point | 95–96 °C (203–205 °F; 368–369 K) |
Boiling point | 305 °C (581 °F; 578 K) |
Hazards | |
GHS labelling: | |
![]() | |
Warning | |
H315, H319, H335 | |
P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, P501 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
|
Bis(trifluoromethanesulfonyl)aniline is the organic compound with the formula C6H5N(SO2CF3)2.[1] It is a white solid. The compound is used to install the triflyl group (SO2CF3). Its behavior is akin to that of triflic anhydride, but milder.
See also
[edit]- Comins' reagent, a related triflating reagent.
References
[edit]- ^ Zeller, Wayne E.; Schwörer, Ralf (2009). "N-Phenyltrifluoromethanesulfonimide". E-EROS Encyclopedia of Reagents for Organic Synthesis. doi:10.1002/047084289X.rp142.pub2. ISBN 978-0471936237.