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.

1,4-Cyclooctadiene-3-One CAS NO 1073-76-3

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CAS No.:1073-76-3

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Content:99.0%

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2,2,6,6-Tetramethyl-3,5-Heptanedione CAS NO 1118-71-4

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CAS No.:1118-71-4

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Dicyclopropyl Ketone CAS NO 1121-37-5

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CAS No.:1121-37-5

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1-Acetylcyclohexanol CAS NO 1123-27-9

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CAS No.:1123-27-9

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1-Cyclohexyl-2-Methylpropan-1-One CAS NO 1125-71-9

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CAS No.:1125-71-9

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2-Oxocyclohexanecarbaldehyde CAS NO 1193-63-1

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CAS No.:1193-63-1

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2,2,9,9-Tetramethyl-3,8-Decanedione CAS NO 1490-36-4

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CAS No.:1490-36-4

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Content:99.90%

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3-Tridecanone CAS NO 1534-26-5

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CAS No.:1534-26-5

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