Pyrazole: Difference between revisions

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[[Category:Heterocyclic compounds]]
[[Category:Heterocyclic compounds]]
[[Category:Pyrazoles]]
[[Category:Pyrazoles]]
<gallery>
File:Pyrazoles_synthesis.png|Pyrazoles synthesis
File:Aryl_camphor-fused_pyrazole_synth.png|Aryl camphor-fused pyrazole synthesis
File:Aryl-alicyclic_quinol-pyrazole_synth.png|Aryl-alicyclic quinol-pyrazole synthesis
File:Aryl-fused_quinol-pyrazole_synth.png|Aryl-fused quinol-pyrazole synthesis
File:Potassium_scorpionate.svg|Potassium scorpionate
File:Lasri_condensation_reaction.svg|Lasri condensation reaction
File:Celecoxib_structure.png|Celecoxib structure
File:Pyrazole_SDHI_intermediate.svg|Pyrazole SDHI intermediate
</gallery>

Latest revision as of 11:36, 18 February 2025

Pyrazole is a class of organic compounds with the molecular formula C3H3N2H. It is a heterocyclic compound characterized by a 5-membered ring of three carbon atoms and two nitrogen atoms.

Chemistry[edit]

Pyrazole forms the core of various important bioactive compounds including celecoxib (a COX-2 inhibitor) and rimonabant (an antiobesity agent). It is also found in various dyes and pigments.

Synthesis[edit]

Pyrazoles are synthesized through the reaction of α,β-unsaturated carbonyl compounds with hydrazine. This method, known as the Knorr pyrazole synthesis, is a classic method for the synthesis of pyrazoles.

Applications[edit]

Pyrazole derivatives have been found to possess a wide range of biological activities, including anti-inflammatory, analgesic, antipyretic, anticancer, antiviral, antibacterial, and antifungal properties. They are also used in the manufacture of dyes, resins, and pharmaceuticals.

See also[edit]

References[edit]

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