Hydrazones

Hydrazones

Hydrazones are nitrogen–nitrogen double-bond compounds formed from the condensation of hydrazines with aldehydes or ketones. They serve as versatile intermediates in pharmaceuticals, heterocycle synthesis, polymer chemistry, and analytical detection. Hydrazones participate in reduction, oxidation, cyclization, and rearrangement reactions. They are crucial in Wolff–Kishner reductions, providing a pathway for deoxygenation of carbonyl groups. In medicinal chemistry, hydrazones contribute to prodrug strategies, metal chelation, and bioactive scaffold design. Their tunable stability and structural diversity make hydrazones valuable components in advanced synthetic and biochemical applications.

Cyclohexanone Tosylhydrazone CAS NO 4545-18-0

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CAS No.:4545-18-0

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Content:99.90%

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2-Methylcyclohexanone Semicarbazone CAS NO 4549-20-6

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CAS No.:4549-20-6

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(1R)-(+)-Camphor p-Tosylhydrazone CAS NO 4573-49-3

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CAS No.:4573-49-3

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1,7,7-Trimethylbicyclo[2.2.1]Heptane-2-Onesemicarbazone CAS NO 4581-48-0

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CAS No.:4581-48-0

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2'-Hydroxychalcone Hydrazone CAS NO 4590-70-9

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CAS No.:4590-70-9

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2-Propanone Isonicotinoyl Hydrazone CAS NO 4813-04-1

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CAS No.:4813-04-1

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4-(4-Methylphenyl)-2(3H)-Thiazolone Hydrazone CAS NO 4872-78-0

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CAS No.:4872-78-0

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2-Phenyl-2-Cyclohexen-1-One 2,4-Dinitrophenyl Hydrazone CAS NO 4912-60-1

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CAS No.:4912-60-1

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