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-Penten-1-One, 1-(1-Pyrazolidinyl)- CAS NO 900189-00-6

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CAS No.:900189-00-6

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Content:99.90%

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2-Cyclohexen-1-One,3-(Cyclohexyloxy)-(9Ci) CAS NO 903576-10-3

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CAS No.:903576-10-3

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Cyclohexanone, 2,4-Dichloro- CAS NO 908104-94-9

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CAS No.:908104-94-9

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4-Methyl Bi(Cyclohexyl)-4-One CAS NO 914221-47-9

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CAS No.:914221-47-9

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Cyclohexanone, 2-Chloro-4-Methoxy- CAS NO 927180-14-1

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CAS No.:927180-14-1

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2-Butanone, 4-(2-Thiazolyl)- CAS NO 933740-86-4

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CAS No.:933740-86-4

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4-(Aminomethyl)Cyclohexanone CAS NO 934475-93-1

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CAS No.:934475-93-1

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3-Pentanone, 1,5-Bis(4-Bromophenyl)- CAS NO 937635-98-8

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CAS No.:937635-98-8

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