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.

1-Cyclopentyl-Heptan-1-One CAS NO 660844-13-3

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CAS No.:660844-13-3

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Content:99.90%

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2-Pentanone, 3-Chloro-5-Ethoxy- CAS NO 663179-27-9

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CAS No.:663179-27-9

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5-Octen-7-Yn-2-One, 6-Methyl-, (5Z)- (9Ci) CAS NO 664343-08-2

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CAS No.:664343-08-2

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Ethanone, 1-[(2R)-Tetrahydro-2-Furanyl]- (9Ci) CAS NO 666203-86-7

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CAS No.:666203-86-7

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2-Cyclohexen-1-One,3-Ethyl-6-Methyl-4-(Phenylmethylene)-(9Ci) CAS NO 667937-10-2

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CAS No.:667937-10-2

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Ethanone,2-Bromo-1-(2,2-Difluoro-1,3-Benzodioxol-4-Yl)- CAS NO 668275-94-3

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CAS No.:668275-94-3

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2-Pentanone, 5-Hydroxy-4-Methyl-3-Methylene-, (4R)- (9Ci) CAS NO 668995-06-0

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CAS No.:668995-06-0

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Ethanone, 1-(3,3-Dimethyl-2-Oxetanyl)-2,2,2-Trifluoro- (9Ci) CAS NO 671220-27-2

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CAS No.:671220-27-2

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