Lithium bis(trimethylsilyl)amide 97%
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.[7][6]
Base employed in generating enolates for the preparation of lactone precursors,[2] pyranones,[3] and cyclohexanes.[4]
Used to catalyze the addition of
phosphine P-H bonds to carbodiimides leading to phosphaguanidines.[1] Also used in a novel three-step synthesis of disubstituted 1,2,5-thiadiazoles.[5]
10, 50, 250 g in glass bottle
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