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.

1,2-Dibromo-3-Butanone CAS NO 25109-57-3

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CAS No.:25109-57-3

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Content:99.90%

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3,4-Dimethyl-Hexane-2,5-Dione CAS NO 25234-79-1

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CAS No.:25234-79-1

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Ethanone, 1-(Tetrahydro-2-Furanyl)- CAS NO 25252-64-6

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CAS No.:25252-64-6

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1-Dimethylamino-4-Methyl-Pentan-3-One CAS NO 25287-61-0

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CAS No.:25287-61-0

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1-(1-Hydroxycyclohexyl)Acetone CAS NO 25290-13-5

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CAS No.:25290-13-5

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1,5-Bis(Dimethylamino)-1,4-Pentadien-3-One CAS NO 25299-40-5

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CAS No.:25299-40-5

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Ethanone, 1-(3-Methylenecyclobutyl)- (9Ci) CAS NO 25303-66-6

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CAS No.:25303-66-6

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1-Acetoxy-2-Hydroxy-16-Heptadecen-4-One CAS NO 25346-18-3

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CAS No.:25346-18-3

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