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.

1-(2,5-Dihydroxyphenyl)Ethanone Oxime CAS NO 24558-42-7

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CAS No.:24558-42-7

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Content:99.90%

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Benzaldehyde, 2-Methyl-, Oxime, (E)- (9Ci) CAS NO 24652-62-8

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CAS No.:24652-62-8

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Content:99.90%

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Benzaldehyde, 2-Fluoro-, Oxime, (E)- (9Ci) CAS NO 24652-66-2

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CAS No.:24652-66-2

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Benzophenone o-[(Methylthio)Methyl]Oxime CAS NO 25056-49-9

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CAS No.:25056-49-9

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4-Bromobenzaldehyde Oxime CAS NO 25062-46-8

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CAS No.:25062-46-8

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2,6-Dichlorobenzaldoxime CAS NO 25185-95-9

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CAS No.:25185-95-9

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1,3,4-Thiadiazole-2-Carboxaldehyde, 5-Amino-, Oxime CAS NO 25306-05-2

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CAS No.:25306-05-2

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Cetoxime CAS NO 25394-78-9

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CAS No.:25394-78-9

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