 | This article needs additional citations for
verification. (December 2006) |
Nonaflate, CF
3CF
2CF
2CF
2SO−
3, is the common name given to nonafluorobutanesulfonates, the salts or esters of
perfluorobutanesulfonic acid. Its uses are similar to those of
triflate.
It is a good
leaving group.
[1] It is a substitute for more toxic long-chain
PFAS chemicals.
[2]
- ^ Smith, Michael B.; March, Jerry (2007). March's Advanced Organic Chemistry (6th ed.). John Wiley & Sons. p. 497. ISBN 978-0-471-72091-1.
- ^ Thurlow, Matthew (December 27, 2018). "Fear and loathing of PFAS". American Bar Association. Retrieved 19 December 2019.
 | This chemistry-related article is a stub. You can help Wikipedia by expanding it. |
| This article needs additional citations for
verification. (December 2006) |
Nonaflate, CF
3CF
2CF
2CF
2SO−
3, is the common name given to nonafluorobutanesulfonates, the salts or esters of
perfluorobutanesulfonic acid. Its uses are similar to those of
triflate.
It is a good
leaving group.
[1] It is a substitute for more toxic long-chain
PFAS chemicals.
[2]
- ^ Smith, Michael B.; March, Jerry (2007). March's Advanced Organic Chemistry (6th ed.). John Wiley & Sons. p. 497. ISBN 978-0-471-72091-1.
- ^ Thurlow, Matthew (December 27, 2018). "Fear and loathing of PFAS". American Bar Association. Retrieved 19 December 2019.
|
| This chemistry-related article is a stub. You can help Wikipedia by expanding it. |