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.

4-Methoxypent-3-En-2-One CAS NO 2845-83-2

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CAS No.:2845-83-2

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Content:99.90%

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2-Heptadecanone CAS NO 2922-51-2

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CAS No.:2922-51-2

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3-Eicosanone CAS NO 2955-56-8

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CAS No.:2955-56-8

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3,8-Decanedione CAS NO 2955-63-7

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CAS No.:2955-63-7

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Cyclopropene-3-One CAS NO 2961-80-0

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CAS No.:2961-80-0

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3,3-Dimethylcyclohexanone CAS NO 2979-19-3

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CAS No.:2979-19-3

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4-(Benzyloxy)Cyclohexanone CAS NO 2987-06-6

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CAS No.:2987-06-6

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Content:99.90%

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Ethanone, 1-(2-Ethenylcyclopropyl)- (9Ci) CAS NO 20036-40-2

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CAS No.:20036-40-2

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