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-(2,6-Dichlorobenzyl)Pentane-2,4-Dione CAS NO 175136-81-9

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CAS No.:175136-81-9

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Cyclohexyl 2-(3-Methoxyphenyl)Ethyl Ketone CAS NO 175234-19-2

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CAS No.:175234-19-2

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Oxazolidine, 3-Acetyl-2,4,4-Trimethyl- (9Ci) CAS NO 175553-70-5

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CAS No.:175553-70-5

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5-Hepten-2-One, 5-Ethyl-, (E)- (9Ci) CAS NO 175655-42-2

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CAS No.:175655-42-2

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2,3,6-Heptanetrione (9Ci) CAS NO 176237-95-9

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CAS No.:176237-95-9

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6-Heptyn-2-One, 5-Methylene- (9Ci) CAS NO 176541-67-6

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CAS No.:176541-67-6

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2-Pentanone, 3-[(Methylthio)Methylene]- (9Ci) CAS NO 176646-21-2

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CAS No.:176646-21-2

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Ethanone, 1-[2-(1-Hexenyl)Cyclopropyl]-, [1S-[1Alpha,2Alpha(Z)]]- (9Ci) CAS NO 177853-64-4

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CAS No.:177853-64-4

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