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.

(E)-2-(1-(4,5-Dihydro-1H-Imidazol-2-Yl)Ethoxy)Benzaldehyde Oxime CAS NO 1043533-83-0

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CAS No.:1043533-83-0

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Content:99.90%

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1-(2-Ethoxyphenyl)Ethanone Oxime CAS NO 1051939-38-8

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CAS No.:1051939-38-8

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3,4-Dichloro-Alpha-Chlorobenzaldoxime CAS NO 1056189-27-5

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CAS No.:1056189-27-5

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(Z)-5H-Cyclopenta[B]Pyridin-7(6H)-One o-Methyl Oxime CAS NO 1071727-78-0

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CAS No.:1071727-78-0

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5-Methoxynicotinaldehyde Oxime CAS NO 1087659-31-1

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CAS No.:1087659-31-1

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(4-Chlorophenyl)(Oxo)Acetaldehyde Oxime CAS NO 1089304-84-6

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CAS No.:1089304-84-6

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Content:99.90%

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6-Bromo-2-Chloronicotinaldehyde Oxime CAS NO 1142192-25-3

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CAS No.:1142192-25-3

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Content:99.90%

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5,6-Dimethoxynicotinaldehyde Oxime CAS NO 1138443-93-2

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CAS No.:1138443-93-2

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Content:99.90%

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