CAS 2273-41-8
:α,α-Dimethyl-1-piperidineacetonitrile
Description:
α,α-Dimethyl-1-piperidineacetonitrile, with the CAS number 2273-41-8, is an organic compound characterized by its piperidine ring structure, which is a six-membered saturated nitrogen-containing heterocycle. This compound features a nitrile functional group (-C≡N) attached to a carbon chain that is further substituted with two methyl groups at the alpha position relative to the piperidine nitrogen. The presence of the nitrile group contributes to its polar nature, influencing its solubility in various organic solvents. Typically, compounds like α,α-Dimethyl-1-piperidineacetonitrile are utilized in organic synthesis and may serve as intermediates in the production of pharmaceuticals or agrochemicals. Its chemical properties include potential reactivity due to the nitrile group, which can participate in nucleophilic addition reactions. Safety data should be consulted for handling, as with many organic compounds, it may pose health risks if not managed properly. Overall, this compound exemplifies the diverse functionalities that can arise from simple structural modifications in organic chemistry.
Formula:C9H16N2
InChI:InChI=1S/C9H16N2/c1-9(2,8-10)11-6-4-3-5-7-11/h3-7H2,1-2H3
InChI key:InChIKey=IGSJLBUPRRXRDY-UHFFFAOYSA-N
SMILES:C(C#N)(C)(C)N1CCCCC1
Synonyms:- 1-Piperidineacetonitrile, .alpha.,.alpha.-dimethyl-
- 1-Piperidineacetonitrile, α,α-dimethyl-
- 2-Piperidino-2-cyanopropane
- NSC 150245
- α,α-Dimethyl-1-piperidineacetonitrile
- 2-Methyl-2-(piperidin-1-yl)propanenitrile
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Found 1 products.
a,a-Dimethyl-1-piperidineacetonitrile
CAS:Controlled Product<p>Dimethylcyanamide is an organic compound that can be synthesized from cyanide or cyanic acid. Dimethylcyanamide is a colorless liquid with a strong odor. It has been used in the past as a precursor to other compounds, but it has since been replaced by cheaper and more convenient methods. Dimethylcyanamide reacts with primary amines to form nitriles, which are useful intermediates in organic synthesis. In addition, the reaction of dimethylcyanamide with secondary amines leads to the formation of primary amines. The transamination of dimethylamine-N-oxide yields a-dimethylaminopropionitrile as an intermediate product. The elimination reaction mechanism for this process involves the conversion of ammonia into hydroxide ions and hydrogen gas. This reaction produces high yields for both products and does not require high temperatures or pressures.</p>Formula:C9H16N2Purity:Min. 95%Molecular weight:152.24 g/mol
