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1.1.3.3- Tetramethylbutyl isonitrile

N-( 1-butyl-lithium, 1,1,3,3-tetramethylbutyl isonitrile, and deuterium oxide,... [Pg.75]

Tetramethylbutyl isonitrile, from N-( 1,1,3,3-tetramethy lbutyl)-for-mamide and thionyl chloride, 51, 31... [Pg.77]

Isonitriles are presumed to be toxic, and it is recommended that the workup procedure be performed in a hood. Unlike most isonitriles, however, 1,1,3,3-tetramethylbutyl isonitrile is not malodorous. It has a sweetish pine odor, which becomes unpleasant only after continued inhalation. [Pg.18]

Aldehydes from 1,1,3,3-Tetramethylbutyl isonitrile and Organometallic Reagents... [Pg.20]

A. 1,1,3,3-Tetramethylbutyl isonitrile. A 3-1. three-necked round-bottomed flask is fitted with a Hershberg stirrer, a fiOO-ml. pressure-equalizing addition funnel, and a nitrogen gas... [Pg.100]

The molar amount of 1,1,3,3-tetramethylbutyl isonitrile used is equivalent to the Grignard reagent content. [Pg.103]

See other pages where 1.1.3.3- Tetramethylbutyl isonitrile is mentioned: [Pg.56]    [Pg.133]    [Pg.75]    [Pg.76]    [Pg.20]    [Pg.79]    [Pg.101]    [Pg.112]    [Pg.33]    [Pg.38]    [Pg.229]    [Pg.221]   


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1.1.3.3- Tetramethylbutyl isonitrile chloride

1.1.3.3- Tetramethylbutyl isonitrile, from

Benzaldehyde, by condensation phenyllithium with 1,1,3,3-tetramethylbutyl isonitrile

Isonitril

Isonitrile

Isonitriles

Isonitriles 1.1.3.3- tetramethylbutyl

Isonitriles 1.1.3.3- tetramethylbutyl

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