trimethyl(1,1,2,2-tetrafluoro-2-(phenylthio)ethyl)silane Chemische Eigenschaften,Einsatz,Produktion Methoden

Verwenden

After being activated with silicophilic activators, like fluorides, alkoxides or carboxylates, phenylsulfanyltetrafluoroethyl trimethylsilane acts as nucleophilic phenylsulfanyltetrafluoroethylation reagent towards electrophiles such as aromatic aldehydes. A phenylsulfanyltetrafluoroethyl moiety incorporated in the substrate can be treated with tributyltin hydride and generate the corresponding fluoroalkyl radical. If the substrate lacks any olefins, it can be reduced to tetrafluoroethyl group whereas if the substrate contains an olefin in the correct spatial orientation, it can lead to an intramolecular cyclization affording tetrafluorinated cyclic structures.

trimethyl(1,1,2,2-tetrafluoro-2-(phenylthio)ethyl)silane Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte

trimethyl(1,1,2,2-tetrafluoro-2-(phenylthio)ethyl)silane Anbieter Lieferant Produzent Hersteller Vertrieb H?ndler.

Firmenname	Telefon	E-Mail	Land	Produktkatalog	Edge Rate
Dalian Shuanghang Chemical Co., LTD	+86-411-66858498 +86-13941194417	sales@dl-bykj.cn	China	1972	58
TCI (Shanghai) Chemical Trading Co., Ltd.	021-021-61109150	sales@tcisct.com	China	31119	58
Merck KGaA	21-20338288	ordercn@merckgroup.com	China	6394	58

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• trimethyl(1,1,2,2-tetrafluoro-2-(phenylthio)ethyl)silane
• trimethyl(1,1,2,2-tetrafluoro-2-(phenylsulfanyl)ethyl)silane
• Benzene, [[1,1,2,2-tetrafluoro-2-(trimethylsilyl)ethyl]thio]-
• 1000293-91-3