Skip to Content
MilliporeSigma
All Photos(1)

Key Documents

CF0022

Sigma-Aldrich

Phenylsulfanyltetrafluoroethyl trimethylsilane

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
C11H14F4SSi
CAS Number:
MDL number:
UNSPSC Code:
12352101

form

liquid

reaction suitability

reaction type: C-C Bond Formation

Application

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.

Automate your fluorination reactions with Synple Automated Synthesis Platform (SYNPLE-SC002)

Legal Information

Product of CF Plus Chemicals.

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Sorry, we don't have COAs for this product available online at this time.

If you need assistance, please contact Customer Support.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Articles

The fluoroalkylation toolbox now includes Togni reagents, hypervalent iodine perfluoroalkylation reagents, fluoroalkyl bromides, silanes, carboxylates, and sulfonyl fluorides for late stage fluoroalkylation.

The fluoroalkylation toolbox now includes Togni reagents, hypervalent iodine perfluoroalkylation reagents, fluoroalkyl bromides, silanes, carboxylates, and sulfonyl fluorides for late stage fluoroalkylation.

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service