Home Chemistry Heterocyclic Building Blocks Pyridines Nicotinonitrile
Nucleophilic Substitution: Nicotinonitrile can undergo nucleophilic substitution reactions at the carbon atom adjacent to the nitrogen atom. This can result in the replacement of the nitrile group with other nucleophiles, such as hydroxide ions (OH⁻), amines, or thiolates.
Hydrolysis: Nicotinonitrile can undergo hydrolysis under acidic or basic conditions, leading to the cleavage of the carbon-nitrogen triple bond and the formation of carboxylic acids or amides, depending on the reaction conditions.
Reduction: Nicotinonitrile can be reduced to form various derivatives, such as pyridine or piperidine, by using reducing agents like hydrogen gas (H2) in the presence of a catalyst (e.g., Raney nickel) or metal hydrides (e.g., lithium aluminum hydride, LAH).
Addition Reactions: Nicotinonitrile can undergo addition reactions with electrophiles, such as acids or alkylating agents, at the nitrogen or carbon atoms, resulting in the formation of substituted derivatives.
Ring-Forming Reactions: Nicotinonitrile can participate in ring-forming reactions, such as cyclization or condensation reactions, leading to the formation of heterocyclic compounds containing nitrogen atoms in the ring structure.
Oxidation: Nicotinonitrile can undergo oxidation reactions to form various oxidation products, such as nicotinic acid or its derivatives.
Framework+−
By Key Group+−
By Parent Nucleus+−
By Functional Group+−
Heterocyclic related+−
Formula Weight+−
click to sign in and save
5-(Aminomethyl)nicotinonitrile hydrochloride
* Country/Region
* Quantity Required :
* Cat. No.:
* CAS No :
* Product Name :
* Additional Information :