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.

Cyclohexanal Semicarbazone CAS NO 1589-61-3

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CAS No.:1589-61-3

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4-Heptanone 2,4-Dinitrophenyl Hydrazone CAS NO 1655-41-0

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CAS No.:1655-41-0

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Benzaldehyde (Phenylsulfonyl)Hydrazone CAS NO 1666-16-6

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CAS No.:1666-16-6

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Benzaldehyde Tosylhydrazone CAS NO 1666-17-7

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CAS No.:1666-17-7

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4-Hydroxybutyraldehyde 2,4-Dinitrophenyl Hydrazone CAS NO 1708-33-4

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CAS No.:1708-33-4

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2-Pentanone Thiosemicarbazone CAS NO 1752-39-2

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CAS No.:1752-39-2

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1-Phenylcyclopentanecarbaldehyde 2,4-Dinitrophenyl Hydrazone CAS NO 1812-68-6

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CAS No.:1812-68-6

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1-Phenylcyclobutanecarbaldehyde 2,4-Dinitrophenyl Hydrazone CAS NO 1812-69-7

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CAS No.:1812-69-7

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