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-Pentadecanone, 1,1,1-Trifluoro- CAS NO 81123-99-1

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CAS No.:81123-99-1

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Content:99.90%

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1,1,1-Trifluorononadecan-2-One CAS NO 81124-01-8

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CAS No.:81124-01-8

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Pentane-2,4-Dione CAS NO 81235-32-7

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CAS No.:81235-32-7

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3-(Nitromethyl)Cyclopentanone CAS NO 81266-47-9

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CAS No.:81266-47-9

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Ethanone, 1-(1-Chloro-2-Methyl-2-Cyclopenten-1-Yl)- CAS NO 81454-83-3

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CAS No.:81454-83-3

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Bicyclo[4.2.0]Octan-7-One, 8-Chloro- CAS NO 81456-81-7

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CAS No.:81456-81-7

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1-Hydroxy-2-Nonyn-4-One CAS NO 81474-56-8

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CAS No.:81474-56-8

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3-Buten-2-One, 4-(Dimethylamino)-3-Methyl-, (E)- (9Ci) CAS NO 81609-26-9

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CAS No.:81609-26-9

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