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.

Cyclohexanone, 2-[[(2-Ethylphenyl)Amino]Methylene]- (9Ci) CAS NO 692266-54-9

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CAS No.:692266-54-9

Grade:Pharmacy Grade

Content:99.90%

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3,3-Dimethyl-2-Butanone CAS NO 75-97-8

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CAS No.:75-97-8

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Content:99.90%

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Methyl Vinyl Ketone CAS NO 78-94-4

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CAS No.:78-94-4

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Chloroacetone CAS NO 78-95-5

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CAS No.:78-95-5

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Content:99.90%

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1,3-Difluorotetrachloroacetone CAS NO 79-51-6

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CAS No.:79-51-6

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Content:99.90%

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1,1,3-Trichlorotrifluoroacetone CAS NO 79-52-7

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CAS No.:79-52-7

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Content:99.90%

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5,5-Dimethyl-3-(Methylamino)-2-Cyclohexen-1-One CAS NO 701-58-6

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CAS No.:701-58-6

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Content:99.90%

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2,2,5,5-Tetramethylcyclohexane-1,3-Dione CAS NO 702-50-1

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CAS No.:702-50-1

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Content:99.90%

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