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.

4-Morpholinocyclohexanone CAS NO 139025-93-7

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CAS No.:139025-93-7

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Content:99.90%

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Cyclobutanone, 2-Chloro-3-Cyclopropyl-3-Methyl- CAS NO 139537-52-3

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CAS No.:139537-52-3

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(3S,5S)-3,5-Bis(tert-Butyldimethylsilyloxy)Cyclohexanone CAS NO 139356-35-7

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CAS No.:139356-35-7

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2-Cyclohexen-1-One,2-Methyl-3-(1-Methylethyl)-(9Ci) CAS NO 139697-80-6

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CAS No.:139697-80-6

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2-Butanone, 4-(1-Hydroxycyclopropyl)- (9Ci) CAS NO 139963-69-2

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CAS No.:139963-69-2

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3,5-Hexadien-2-One, 4-Methoxy-, (E)- (9Ci) CAS NO 140171-39-7

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CAS No.:140171-39-7

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2,4-Hexanedione, 6-Methoxy- (9Ci) CAS NO 140171-42-2

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CAS No.:140171-42-2

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2-Butanone, 3-(Butylimino)-, (E)- (9Ci) CAS NO 140405-47-6

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CAS No.:140405-47-6

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