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-Hydroxy-2-Methyl-1,3-Cyclopentanedione CAS NO 4800-04-8

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CAS No.:4800-04-8

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Content:99.90%

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2-Chlorocyclooctanone CAS NO 4828-34-6

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CAS No.:4828-34-6

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Bicyclo[3.3.1]None-2-En-9-One CAS NO 4844-11-5

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CAS No.:4844-11-5

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3,5-Heptadien-2-One, (Z,E)- (8Ci,9Ci) CAS NO 4857-17-4

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CAS No.:4857-17-4

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Content:99.90%

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4-Isopropylidene-2,2,3,3-Tetramethylcyclobutanone CAS NO 4868-12-6

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CAS No.:4868-12-6

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(Z)-Undec-8-Ene-2,5-Dione CAS NO 4868-21-7

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CAS No.:4868-21-7

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2-Cyclopentylcyclopentanone CAS NO 4884-24-6

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CAS No.:4884-24-6

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Content:99.90%

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4-Cyclohexyl-4-Methylpentan-2-One CAS NO 4927-39-3

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CAS No.:4927-39-3

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