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.

2-Pentanone, 3-Hydroxy-3-Methyl- (8Ci,9Ci) CAS NO 560-24-7

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CAS No.:560-24-7

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Content:99.90%

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2,2-Dimethylcyclohexane-1,3-Dione CAS NO 562-13-0

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CAS No.:562-13-0

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2,2-Dimethyl-3-Pentanone CAS NO 564-04-5

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CAS No.:564-04-5

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2-Methyl-3-Pentanone CAS NO 565-69-5

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CAS No.:565-69-5

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1,4-Cyclohexanedione, 2,5-Dimethyl- CAS NO 583-81-3

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CAS No.:583-81-3

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Content:99.90%

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4-Hydroxy-2-Butanone CAS NO 590-90-9

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CAS No.:590-90-9

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Content:99.90%

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Rarechem Al Bi 0117 CAS NO 599-99-5

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CAS No.:599-99-5

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Content:99.90%

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Cyclopropanone CAS NO 5009-27-8

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CAS No.:5009-27-8

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Content:99.90%

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