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.

Cyclohexanone, 2-Fluoro-2-Methyl-5-(1-Methylethyl)-, (2S,5R)- (9Ci) CAS NO 272114-51-9

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CAS No.:272114-51-9

Grade:Pharmacy Grade

Content:99.90%

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(2R,3R,5S)-3,5-Dimethyl-1-Benzyloxy-2-Hydroxy-8-(4-Methoxyphenoxy)-4-Octanone CAS NO 276690-15-4

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CAS No.:276690-15-4

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Content:99.90%

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2-Cyclopenten-1-One, 2-Acetyl-4-Hydroxy-3,4-Dimethyl- (9Ci) CAS NO 282715-34-8

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CAS No.:282715-34-8

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Content:99.90%

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2-Hexanone, 4-Hydroperoxy- (9Ci) CAS NO 287473-93-2

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CAS No.:287473-93-2

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Content:99.90%

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3-Hexen-2-One, 5-Hydroxy-, (3E,5S)- (9Ci) CAS NO 288153-65-1

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CAS No.:288153-65-1

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Content:99.90%

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Ethanone, 1-Bicyclo[4.2.1]Nona-2,7-Dien-2-Yl- (9Ci) CAS NO 288605-74-3

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CAS No.:288605-74-3

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Content:99.90%

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3-Buten-2-One, 4-Methoxy-3-(Methoxymethyl)-, (3E)- (9Ci) CAS NO 289881-79-4

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CAS No.:289881-79-4

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Content:99.90%

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Cyclopentanone, 3-(3-Butenyl)-2-Methylene- (9Ci) CAS NO 290346-68-8

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CAS No.:290346-68-8

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Content:99.90%

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