Oximes

Oximes

Oximes are nitrogen-containing carbonyl derivatives formed by the reaction of aldehydes or ketones with hydroxylamine. They are widely used in pharmaceuticals, agrochemicals, coordination chemistry, and analytical chemistry. Oximes participate in reduction, Beckmann rearrangement, cyclization, and condensation reactions. They serve as intermediates for amides, nitriles, lactams, and heterocycles. Oximes are key functional groups in antidotes for organophosphate poisoning and precursors for oxime ethers. Their ability to stabilize specific carbonyl isomers makes them valuable in structural analysis and purification. With tunable reactivity and broad utility, oximes remain versatile reagents in synthetic and industrial chemistry.

2-Hydroxyimino-3-Oxo-n-o-Tolyl-Butyramide CAS NO 3014-32-2

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CAS No.:3014-32-2

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Content:99.90%

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1H-Benzimidazole-2-Carboxaldehyde,Oxime(9Ci) CAS NO 3173-92-0

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CAS No.:3173-92-0

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Cycloundecanone Oxime CAS NO 3189-61-5

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CAS No.:3189-61-5

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4-Methylbenzaldehyde Oxime CAS NO 3235-02-7

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CAS No.:3235-02-7

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p-Anisaldehyde Oxime CAS NO 3235-04-9

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CAS No.:3235-04-9

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2,4-Dinitrobenzaldehyde Oxime CAS NO 3236-33-7

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CAS No.:3236-33-7

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2-Chlorocyclohexanoneoxime CAS NO 3238-18-4

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CAS No.:3238-18-4

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(E)-1-(4-Pyridyl)Ethanone o-Acetyl Oxime CAS NO 3240-22-0

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CAS No.:3240-22-0

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