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.

Cyclobutyl Methyl Ketone CAS NO 3019-25-8

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CAS No.:3019-25-8

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Content:99.90%

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3-Bromopentane-2,4-Dione CAS NO 3043-28-5

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CAS No.:3043-28-5

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8-Cyclohexadecanone CAS NO 3100-36-5

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CAS No.:3100-36-5

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trans-3-Penten-2-One CAS NO 3102-33-8

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CAS No.:3102-33-8

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Ch2Coch3 CAS NO 3122-07-4

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CAS No.:3122-07-4

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2-Methyltetrahydrofuran-3-One CAS NO 3188-00-9

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CAS No.:3188-00-9

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2,4-Dimethyl-1-Penten-3-One CAS NO 3212-68-8

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CAS No.:3212-68-8

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2,5-Octanedione CAS NO 3214-41-3

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CAS No.:3214-41-3

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