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.

1-[4-(Methylsulfanyl)Benzylidene]-2-(4-Nitrophenyl)Hydrazine CAS NO 1352193-86-2

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CAS No.:1352193-86-2

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Content:99.90%

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3-Bromo-N'-[(E)-(4-Hydroxy-3-Methoxyphenyl)Methylidene]Benzohydrazide CAS NO 1369997-07-8

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CAS No.:1369997-07-8

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3-[2-(2,4-Dinitrophenyl)Carbonohydrazonoyl]-1,2-Benzenediol CAS NO 1453261-85-2

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CAS No.:1453261-85-2

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N'-[(2E)-3-(Furan-2-Yl)Prop-2-Enoyl]-4-Nitrobenzohydrazide CAS NO 1610501-69-3

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CAS No.:1610501-69-3

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(E)-n-(2-Hydroxybenzylidene)-3-(Naphthalen-1-Yl)-1H-Pyrazole-5-Carbohydrazide CAS NO 1556631-03-8

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CAS No.:1556631-03-8

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2,3,4-Trihydroxybenzaldehyde 2-Benzylhydrazone CAS NO 1798397-91-7

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CAS No.:1798397-91-7

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Benzaldehyde, 2,3,4-Trihydroxy-, Hydrazone CAS NO 1865681-56-6

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CAS No.:1865681-56-6

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n-Valeraldehyde 2,4-Dinitrophenylhydrazone CAS NO 2057-84-3

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CAS No.:2057-84-3

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