CAS 31865-37-9
:Cyclohexanecarbonitrile, 4-(1,1-dimethylethyl)-
Description:
Cyclohexanecarbonitrile, 4-(1,1-dimethylethyl)-, also known by its CAS number 31865-37-9, is an organic compound characterized by a cyclohexane ring substituted with a carbonitrile group and a tert-butyl group at the para position. This compound typically appears as a colorless to pale yellow liquid or solid, depending on the temperature. It is known for its relatively low volatility and moderate solubility in organic solvents, while being less soluble in water due to the presence of the hydrophobic cyclohexane structure. The carbonitrile functional group contributes to its reactivity, making it useful in various chemical syntheses and applications, including as an intermediate in the production of pharmaceuticals and agrochemicals. Additionally, the tert-butyl group enhances the steric bulk around the reactive sites, influencing its chemical behavior and interactions. Safety data indicates that, like many nitriles, it should be handled with care due to potential toxicity and irritant properties.
Formula:C11H19N
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Found 1 products.
4-tert-Butylcyclohexane-1-carbonitrile
CAS:4-tert-Butylcyclohexane-1-carbonitrile is a versatile chemical that can be used as a reagent in organic synthesis. It is a Grignard reagent, which is an alkoxide of magnesium that reacts with an alkyl halide to form an alcohol or an ether. The 4-tert-butylcyclohexane-1-carbonitrile can also be used for the arylation of ketones and for the stereospecific alkylation of primary amines. This compound has been shown to be effective in the deprotonation of tertiary amines and in the formation of cyclic carbonates. The nature of this molecule is chiral, giving it two possible structures: (R) and (S).Formula:C11H19NPurity:Min. 95%Molecular weight:165.27 g/mol
