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-Hydroxyphenyl)Ethan-1-One Oxime CAS NO 1196-29-8

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CAS No.:1196-29-8

Grade:Pharmacy Grade

Content:99.0%

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Dicyclopropyl Ketoxime CAS NO 1453-52-7

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CAS No.:1453-52-7

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(4-Chlorophenyl)Acetone Oxime CAS NO 1454-65-5

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CAS No.:1454-65-5

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Di-2-Pyridyl Ketoxime CAS NO 1562-95-4

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CAS No.:1562-95-4

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Content:99.90%

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2-Hydroxy-5-Nitrobenzaldehyde Oxime CAS NO 1595-15-9

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CAS No.:1595-15-9

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Content:99.90%

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(E)-4-Pyridinecarbaldehyde Oxime CAS NO 1637-52-1

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CAS No.:1637-52-1

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Content:99.90%

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5-Nonanone Semicarbazone CAS NO 1669-37-0

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CAS No.:1669-37-0

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Content:99.90%

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1-Pyridin-2-Ylethan-1-One Oxime CAS NO 1758-54-9

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CAS No.:1758-54-9

Grade:Pharmacy Grade

Content:99.90%

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