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SODIUM (2-THIENYL)DIMETHYLSILANOLATE, 2M in methyltetrahydrofuran
Product data and descriptions listed are typical values, not intended to be used as specification.
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.
Sodium (4-methylphenyl)dimethylsilanolate
Specific Gravity: 0.961
Flashpoint: -14°C (7°F)
HMIS Key: 2-4-1-X
Hydrolytic Sensitivity: 5: forms reversible hydrate
Formula: C6H9NaOSSi
Application: Sodium silanolate generated "in-situ".1
Reference: 1. Denmark, S. E.; Baird, J. D. Org. Lett. 2006, 8, 793.
Silanes
Silanes
Silicon-Based Cross-Coupling Reagents
Enabling Synthetic Organic Transformations
Silicon-Based Formation of Carbon-Carbon Bonds – Larson