Aliphatic Ketones (including Enols)

Aliphatic Ketones (including Enols)

Aliphatic ketones and their enol forms are widely used reagents in organic synthesis, polymer chemistry, fragrances, and industrial formulations. Their carbonyl functionality enables nucleophilic addition, condensation, oxidation, Grignard reactions, and metal-catalyzed transformations. Enols and enolates serve as reactive intermediates in carbon–carbon bond formation, aldol reactions, and heterocycle construction. Aliphatic ketones also function as solvents, plasticizer components, and extraction agents. Their volatility, polarity, and predictable reactivity patterns support applications in coatings, adhesives, and chemical manufacturing. With tunable steric and electronic properties, aliphatic ketones remain fundamental tools in fine chemical synthesis and process chemistry.

2-Cyclohexen-1-One,3-(Methoxymethoxy)-5-Methyl-(9Ci) CAS NO 95682-12-5

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CAS No.:95682-12-5

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Content:99.90%

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3,4-Octadien-2-One (9Ci) CAS NO 95887-52-8

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CAS No.:95887-52-8

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3-tert-Butylcyclobut-2-Enone CAS NO 95904-85-1

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CAS No.:95904-85-1

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3,5-Hexadien-2-One, 4,5-Dimethyl-, (E)- (9Ci) CAS NO 96219-38-4

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CAS No.:96219-38-4

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Ethanone, 1-(4-Methyl-1,2-Dithiolan-4-Yl)- (9Ci) CAS NO 96285-29-9

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CAS No.:96285-29-9

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5-Undecen-4-One,7-Ethyl-2-Methyl- CAS NO 96446-43-4

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CAS No.:96446-43-4

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Ethanone, 1-(2,3-Dichlorocyclobutyl)-, (1Alpha,2Alpha,3Beta)- (9Ci) CAS NO 96660-50-3

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CAS No.:96660-50-3

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Ethanone, 1-(2,2-Dichlorocyclobutyl)- (9Ci) CAS NO 96660-97-8

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CAS No.:96660-97-8

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