Final Thoughts on Chemistry for 175136-62-6

This compound(Tris(3,5-bis(trifluoromethyl)phenyl)phosphine)Application In Synthesis of Tris(3,5-bis(trifluoromethyl)phenyl)phosphine was discussed at the molecular level, the effects of temperature and reaction time on the properties of the compound were discussed, and the optimum reaction conditions were selected.

Meguro, Tomohiro; Terashima, Norikazu; Ito, Harumi; Koike, Yuka; Kii, Isao; Yoshida, Suguru; Hosoya, Takamitsu published an article about the compound: Tris(3,5-bis(trifluoromethyl)phenyl)phosphine( cas:175136-62-6,SMILESS:FC(C1=CC(C(F)(F)F)=CC(P(C2=CC(C(F)(F)F)=CC(C(F)(F)F)=C2)C3=CC(C(F)(F)F)=CC(C(F)(F)F)=C3)=C1)(F)F ).Application In Synthesis of Tris(3,5-bis(trifluoromethyl)phenyl)phosphine. Aromatic heterocyclic compounds can be classified according to the number of heteroatoms or the size of the ring. The authors also want to convey more information about this compound (cas:175136-62-6) through the article.

Efficient formation of H2O- and air-stable aza-ylides was achieved using the Staudinger reaction between electron-deficient aromatic azides such as 2,6-dichlorophenyl azide and triarylphosphines. The reaction proceeds rapidly and was successfully applied to chem. modification of proteins in living cells.

This compound(Tris(3,5-bis(trifluoromethyl)phenyl)phosphine)Application In Synthesis of Tris(3,5-bis(trifluoromethyl)phenyl)phosphine was discussed at the molecular level, the effects of temperature and reaction time on the properties of the compound were discussed, and the optimum reaction conditions were selected.

Reference:
Piperidine – Wikipedia,
Piperidine | C5H11N – PubChem