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.

(5S)-5-[(R)-1-Hydroxy-1,5-Dimethyl-4-Hexenyl]-2-Methyl-2-Cyclohexen-1-One CAS NO 35346-20-4

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CAS No.:35346-20-4

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Content:99.90%

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5-Cyclooctene-1,2-Dione CAS NO 35353-89-0

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CAS No.:35353-89-0

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Cyclohexanone, 2-Chloro-2-Fluoro- CAS NO 35365-22-1

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CAS No.:35365-22-1

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2-(Methoxymethyl)Cyclopentanone CAS NO 35457-02-4

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CAS No.:35457-02-4

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2-Dodecylcyclobutanone CAS NO 35493-46-0

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CAS No.:35493-46-0

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2,2,5,5-Tetramethyl-3-Methylene-1-Cyclohexanone CAS NO 35505-97-6

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CAS No.:35505-97-6

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3,5-Heptadien-2-One, (Z,Z)- (9Ci) CAS NO 35694-38-3

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CAS No.:35694-38-3

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4-Pentene-2,3-Dione, 4-Methyl- (9Ci) CAS NO 35749-74-7

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CAS No.:35749-74-7

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