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Noncyclic Open-Chained Organosilyl Nitrogen Compounds

1 Noncyclic (Open-Chained) Organosilyl Nitrogen Compounds [Pg.72]

Aminotrimethylsilane has not been isolated as a pure substance [362] because it condenses very easily (Eq. 3.175)  [Pg.72]

This reaction proceeds rapidly at 100 °C and can be monitored by measurement of the hydrogen evolved. [Pg.72]

Alkyllithium may be used in place of the metal hydride, e.g. for the preparation of [Pg.72]

Aminoorganosilanes may also be made by the reaction of Schilfs bases with haloorganosilanes in the presence of a catalyst, for example palladium(II) chloride (Eq. 3.177)  [Pg.73]




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Chain compounds

Noncyclic compounds

Open-Chain Compounds

Open-chain

Organosilyls

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