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.

(4R)-4-Acetyl-3,4Α-Dihydroxy-5Β-(3-Methyl-2-Butenyl)-2-(3-Methyl-1-Oxobutyl)-2-Cyclopenten-1-One CAS NO 18445-45-9

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CAS No.:18445-45-9

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5-Pentyl-Cyclohexane-1,3-Dione CAS NO 18456-88-7

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CAS No.:18456-88-7

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1-[(R)-3-Methyl-2-(3-Isopropylfuran-2-Yl)-1-Cyclopenten-1-Yl]Ethanone CAS NO 18492-61-0

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CAS No.:18492-61-0

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[S,(-)]-4,21,21-Trimethyldocosane-2-One CAS NO 18607-44-8

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CAS No.:18607-44-8

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2-Hexadecanone CAS NO 18787-63-8

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CAS No.:18787-63-8

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4-Acetyltetradecahydro-11H-Benzo[A]Cyclopenta[D]Cycloocten-11-One CAS NO 18938-06-2

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CAS No.:18938-06-2

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2,3-Dichloro-5-(Dichloromethylidene)Cyclopent-2-Ene-1,4-Dione CAS NO 18964-31-3

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CAS No.:18964-31-3

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3,5-Heptadien-2-One, (3E,5E)- (9Ci) CAS NO 18402-90-9

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CAS No.:18402-90-9

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