Non disponible en dehors du Royaume-Uni et de l'Irlande

Application

Base employed in generating enolates for the preparation of lactone precursors, pyranones, and cyclohexanes.Used to catalyze the addition of phosphine P-H bonds to carbodiimides leading to phosphaguanidines. Also used in a novel three-step synthesis of disubstituted 1,2,5-thiadiazoles.

General description

Lithium bis(trimethylsilyl)amide is a non-nucleophilic strong Brønsted base, which is generally soluble in most of the nonpolar organic solvents. It is most commonly employed in organic reactions.

Packaging

10, 50, 250 g in glass bottle