Additional Properties
- HMIS 2-2-1-X
- Molecular Formula C11H19NO3Si
- Molecular Weight (g/mol) 241.36
- TSCA No
- Boiling Point (˚C/mmHg) NA
Application
Extensive review on the use in silicon-based cross-coupling reactions.1
Reference
1. Denmark, S. E. et al. Organic Reactions, Vol. 75, Denmark, S. E. ed., John Wiley and Sons, 233, 2011.
Safety
Arylsilane Cross-Coupling Agent
The cross-coupling reaction is a highly useful methodology for the formation of carbon-carbon bonds. It involves two reagents, with one typically being a suitable organometallic reagent - the nucleophile - and the other a suitable organic substrate, normally an unsaturated halide, tosylate or similar - the electrophile.
3-Pyridyltriethoxysilane; 3-Triethoxysilylpyridine
Silicon Chemistry, Articles
Hatanaka and Hiyama first reported the palladium-catalyzed, fluoride-promoted reaction of aryl, alkenyl, allyl, and ethynyltrimethylsilanes with aryl, vinil and allyl halides to form the respective cross-coupled products