Home Chemistry Heterocyclic building blocks Pyrazoles 1,5-diphenyl-1h-pyrazole
Substitution Reactions: The phenyl groups on the pyrazole ring can undergo substitution reactions. For example, you can perform electrophilic aromatic substitution reactions with reagents like acyl chlorides (Friedel-Crafts acylation) or nitration (to introduce nitro groups).
Reduction: Reduction of the pyrazole ring can be achieved using reducing agents like lithium aluminum hydride (LiAlH4) to convert it to a corresponding piperidine derivative.
Oxidation: Oxidation of 1,5-diphenyl-1H-pyrazole can yield various products, depending on the reaction conditions. For example, you can use strong oxidizing agents like potassium permanganate (KMnO4) to oxidize it to carboxylic acids or other functional groups.
Alkylation: The pyrazole ring can undergo alkylation reactions, where alkyl halides or alkylating agents are used to introduce alkyl groups onto the ring.
Acylation: The pyrazole ring can also undergo acylation reactions using acyl chlorides or anhydrides to introduce acyl groups.
Heterocycle Formation: 1,5-diphenyl-1H-pyrazole can participate in reactions to form other heterocyclic compounds.
Cross-Coupling Reactions: It can be used as a substrate in various cross-coupling reactions, such as Suzuki-Miyaura or Heck coupling, to introduce different substituents on the phenyl groups.
Functional Group Interconversions: You can transform the compound by converting functional groups, such as converting one of the phenyl groups to a different functional group using appropriate reagents.
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5-(4-Chlorophenyl)-1-(2,4-dichlorophenyl)-4-methylpyrazole-3-carboxylic acid
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1,5-Diphenyl-1H-pyrazole-4-carboxylic acid
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Methyl 1,5-diphenyl-1H-pyrazole-3-carboxylate
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Ethyl 1,5-diphenyl-1H-pyrazole-3-carboxylate
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