Home Chemistry Heterocyclic building blocks Pyridazines 3-phenylpyridazine
Reduction: 3-Phenylpyridazine can be reduced using various reducing agents, such as hydrogen gas H2 with a catalyst (e.g., palladium on carbon), sodium borohydride (NaBH4), or lithium aluminum hydride (LiAlH4). Reduction can lead to the formation of the corresponding dihydro compound.
Oxidation: Oxidation reactions can be carried out on 3-phenylpyridazine to convert it into various functional groups. For instance, oxidation with strong oxidizing agents like potassium permanganate (KMnO4) or chromium(VI) reagents can lead to the formation of pyridazine carboxylic acids or other oxidized products.
Nucleophilic Substitution: The nitrogen atoms in the pyridazine ring can undergo nucleophilic substitution reactions with appropriate electrophiles. This could include reactions with alkyl halides to form N-alkylated derivatives.
Heterocycle Formation: 3-Phenylpyridazine can participate in various heterocycle-forming reactions, such as condensation reactions with carbonyl compounds (e.g., ketones or aldehydes) to produce pyridazine-fused heterocycles.
Acylation and Alkylation: 3-Phenylpyridazine can undergo acylation and alkylation reactions when treated with acylating agents (e.g., acyl chlorides) or alkylating agents (e.g., alkyl halides) in the presence of suitable catalysts.
Catalytic Hydrogenation: The double bonds in the pyridazine ring can be selectively hydrogenated using hydrogen gas and a suitable catalyst to produce saturated derivatives.
Framework+−
By Key Group+−
By Parent Nucleus+−
By Functional Group+−
Formula Weight+−
* Country/Region
* Quantity Required :
* Cat. No.:
* CAS No :
* Product Name :
* Additional Information :