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.

3-(2-Amino-Phenylamino)-5,5-Dimethyl-Cyclohex-2-Enone CAS NO 39222-69-0

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CAS No.:39222-69-0

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Content:99.90%

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Ethanone, 2-Chloro-1,2-Dicyclopropyl- (9Ci) CAS NO 39250-97-0

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CAS No.:39250-97-0

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Ethanone, 1-(2-Methylcyclobutyl)-, cis- (9Ci) CAS NO 39257-06-2

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CAS No.:39257-06-2

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Ethanone, 1-(2-Methylcyclobutyl)-, trans- (9Ci) CAS NO 39257-07-3

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CAS No.:39257-07-3

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3-Cyclohexen-1-One,3-Methoxy-2-(1-Methylethyl)-(9Ci) CAS NO 342801-15-4

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CAS No.:342801-15-4

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Cyclohexanone, 3-Methyl-5-(1-Methylethyl)-, (3S,5S)- (9Ci) CAS NO 342813-29-0

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CAS No.:342813-29-0

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3-Penten-2-One, 4-Propoxy-, (3Z)- (9Ci) CAS NO 342909-78-8

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CAS No.:342909-78-8

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Ethanone, 1-(3-Ethylcyclopentyl)- (9Ci) CAS NO 343269-73-8

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CAS No.:343269-73-8

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