Home Chemistry Heterocyclic building blocks Pyrazoles 1-cyclopropyl-1h-pyrazole
Acylation: The pyrazole nitrogen atoms can be acylated by reacting with acyl chlorides or anhydrides in the presence of a base to form N-acyl derivatives.
Alkylation: You can alkylate the pyrazole ring by using alkyl halides or alkylating agents under suitable conditions. This leads to the introduction of alkyl groups on the pyrazole nitrogen atoms.
Ring Opening: The cyclopropyl ring can be opened under certain conditions, leading to the formation of a linear compound.
Cyclization Reactions: 1-Cyclopropyl-1H-pyrazole can participate in cyclization reactions to form various fused ring systems, depending on the reaction conditions and reagents.
Reduction: The cyclopropyl group can be reduced to a cyclopropylmethyl group using reducing agents such as lithium aluminum hydride (LiAlH4) or hydrogen gas H2 with a suitable catalyst.
Oxidation: Oxidation reactions can be employed to convert the cyclopropyl group into other functional groups.
Metalation: The pyrazole ring can undergo metalation reactions, where a metal atom or group replaces a hydrogen atom on the ring. This can serve as a key step in various synthetic pathways.
Condensation Reactions: 1-Cyclopropyl-1H-pyrazole can participate in condensation reactions to form heterocyclic compounds or other products.
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1-(Cyclopropyl)-1H-pyrazole-4-carbaldehyde
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1-Cyclopropyl-1H-pyrazole-4-carboxylic acid
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1-Cyclopropyl-1H-pyrazole-3-carboxylic acid
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