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-Cyclohexyl-4,4-Diethoxy-1-Butanone CAS NO 55402-06-7

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CAS No.:55402-06-7

Grade:Pharmacy Grade

Content:99.90%

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1-Piperidino-2-Ethyl-1-Butanone CAS NO 55581-66-3

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CAS No.:55581-66-3

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Content:99.90%

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3,5-Hexadien-2-One, 4-Methyl- (6Ci,9Ci) CAS NO 55626-68-1

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CAS No.:55626-68-1

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Content:99.90%

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5-(1,2-Propadienyloxy)-2-Pentanone CAS NO 55702-69-7

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CAS No.:55702-69-7

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Content:99.90%

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2-Pentanone, 5-(2-Propynyloxy)- CAS NO 55702-70-0

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CAS No.:55702-70-0

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4-Penten-2-One, 3-Hydroxy-3-Methyl- (9Ci) CAS NO 55795-29-4

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CAS No.:55795-29-4

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Content:99.90%

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1,3-Dicyclohexyl-1,3-Propanedione CAS NO 55846-67-8

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CAS No.:55846-67-8

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Content:99.90%

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1-Cyclopentyl-3-Phenyl-1,3-Propanedione CAS NO 55846-71-4

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CAS No.:55846-71-4

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Content:99.90%

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