Chemistry:Bis(trifluoromethanesulfonyl)aniline
From HandWiki
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| Names | |
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| Preferred IUPAC name
1,1,1-Trifluoro-N-phenyl-N-(trifluoromethanesulfonyl)methanesulfonamide | |
| Other names
Phenyl triflimide
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| Identifiers | |
3D model (JSmol)
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| 1269141 | |
| ChemSpider | |
| EC Number |
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PubChem CID
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| UNII | |
CompTox Dashboard (EPA)
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| 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 pictograms | 
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| GHS Signal word | Warning |
| H315, H319, H335 | |
| P261, P264, P271, P280, P302+352, P304+340, P305+351+338, P312, P321, P332+313, P337+313, P362, P403+233, P405, P501 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| Infobox references | |
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
- Comins' reagent, a related triflating reagent.
References
- ↑ 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.
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