CAS 2978-30-5
:2,2-dimethylpent-4-enenitrile
Description:
2,2-Dimethylpent-4-enenitrile is an organic compound characterized by its alkenyl nitrile structure. It features a pentene backbone with a double bond located at the fourth carbon and two methyl groups attached to the second carbon, contributing to its branched structure. The presence of the nitrile functional group (-C≡N) imparts notable properties, including polarity and the ability to participate in nucleophilic reactions. This compound is typically a colorless to pale yellow liquid with a distinctive odor. It is soluble in organic solvents but has limited solubility in water due to its hydrophobic hydrocarbon chain. 2,2-Dimethylpent-4-enenitrile can be used in various chemical syntheses and may serve as an intermediate in the production of pharmaceuticals or agrochemicals. Safety considerations include handling it in well-ventilated areas and using appropriate personal protective equipment, as it may pose health risks upon exposure. Overall, its unique structure and functional groups make it a valuable compound in organic chemistry.
Formula:C7H11N
InChI:InChI=1/C7H11N/c1-4-5-7(2,3)6-8/h4H,1,5H2,2-3H3
SMILES:C=CCC(C)(C)C#N
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Found 2 products.
2,2-Dimethylpent-4-enenitrile
CAS:2,2-Dimethylpent-4-enenitrilePurity:97%Molecular weight:109.17g/mol2,2-Dimethylpent-4-enenitrile
CAS:<p>2,2-Dimethylpent-4-enenitrile is an organic compound that can be synthesized by the reaction of bromomethyl cyclopropane with a Grignard reagent. It is a useful synthetic intermediate for the synthesis of imines and carbonitriles. Grignard reagents are nucleophilic and react with alkenes to form addition products called imines. 2,2-Dimethylpent-4-enenitrile is a cyclic molecule that reacts with nucleophiles such as Grignard reagents in a nucleophilic substitution reaction. The addition product formed is known as an imine.</p>Formula:C7H11NPurity:Min. 95%Molecular weight:109.17 g/mol

