Bisphenol AF
Bisphenol AF (BPAF) is a fluorinated organic compound related to bisphenol A in which the two methyl groups are replaced with trifluoromethyl groups.
 | |
| Names | |
|---|---|
| IUPAC name
4-[1,1,1,3,3,3-Hexafluoro-2-(4-hydroxyphenyl)propan-2-yl]phenol | |
| Other names
Biphenol AF; Hexafluorobisphenol A; Hexafluorodiphenylolpropane; Bisphenol A hexafluoride; 4,4'-(Hexafluoroisopropylidene)diphenol; Hexafluoroacetone bisphenol A; 2,2-Bis(4-hydroxyphenyl)hexafluoropropane | |
| Identifiers | |
3D model (JSmol) |
|
| Abbreviations | BPAF |
| ChemSpider | |
| ECHA InfoCard | 100.014.579 |
PubChem CID |
|
| UNII | |
CompTox Dashboard (EPA) |
|
| |
| |
| Properties | |
| C15H10F6O2 | |
| Molar mass | 336.233 g·mol−1 |
| Melting point | 162 °C[1] |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
  | |
| Infobox references | |
Whereas BPA binds with human estrogen-related receptor gamma (ERR-γ), BPAF all but ignores ERR-γ. Instead, BPAF activates ERR-α and binds to and disables ERR-β.[2]
Analytics
The chemical shifts in 1H, 13C and 19F NMR spectroscopy are given in the literature.[3]
gollark: testbot1, help.
gollark: Apiorestarti nitialized.
gollark: The bots aren't even running. Probably.
gollark: It has some apiodelay.
gollark: oh bees oh bees oh bees oh bees oh bees oh bees oh bees oh bees oh bees oh bees oh bees oh bees oh bees oh bees oh bees oh bees oh bees oh bees oh bees oh bees oh bees oh bees oh bees oh bees oh bees oh bees oh bees oh bees oh bees oh bees oh bees oh bees oh bees oh bees oh bees oh bees oh bees oh bees oh bees oh bees oh bees oh bees oh bees oh bees oh bees oh bees oh bees oh bees oh bees oh bees oh bees oh bees oh bees oh bees oh bees oh bees oh bees oh bees oh bees oh bees oh bees oh bees oh bees oh bees oh bees oh bees oh bees oh bees oh bees oh bees oh bees oh bees oh bees oh bees oh bees oh bees oh bees oh bees oh bees oh bees oh bees oh bees oh bees oh bees oh bees oh bees oh bees oh bees oh bees oh bees
See also
References
- Hayasaka, Tatsuya; Katsuhara, Yutaka; Kume, Takashi; Yamazaki, Takashi (2011). "HF-mediated equilibrium between fluorinated ketones and the corresponding α-fluoroalcohols". Tetrahedron. 67 (12): 2215–2219. doi:10.1016/j.tet.2011.01.087.
- Janet Raloff: Another plastics ingredient raises safety concerns, Science News, June 5th, 2010; Vol.177 #12 (p. 14)
- Hayasaka, Tatsuya; Katsuhara, Yutaka; Kume, Takashi; Yamazaki, Takashi (2011). "HF-mediated equilibrium between fluorinated ketones and the corresponding α-fluoroalcohols". Tetrahedron. 67 (12): 2215–2219. doi:10.1016/j.tet.2011.01.087.
This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.