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.

[S,(+)]-2,5-Dimethylheptane-4-One CAS NO 27763-95-7

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CAS No.:27763-95-7

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Content:99.90%

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2-Dimethylamino-1-Phenyl-3-Heptanone CAS NO 27820-08-2

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CAS No.:27820-08-2

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3,4-Diacetyl-3-Hexene-2,5-Dione CAS NO 27871-55-2

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CAS No.:27871-55-2

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2,5-Bis(Hydroxyimino)Cyclopentan-1-One CAS NO 27894-44-6

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CAS No.:27894-44-6

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3-n-Pentyl-2,4-Pentanedione CAS NO 27970-50-9

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CAS No.:27970-50-9

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trans-3,4-Dimethylcyclohexanone CAS NO 28023-45-2

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CAS No.:28023-45-2

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2,2,4-Trimethylcyclopentanone CAS NO 28056-54-4

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CAS No.:28056-54-4

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2,3,3-Trimethylcyclobutanone CAS NO 28290-01-9

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CAS No.:28290-01-9

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