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-[2-(Benzyloxy)-5-Methylphenyl]Ethanone CAS NO 36808-17-0

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CAS No.:36808-17-0

Grade:Pharmacy Grade

Content:99.90%

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Levoglucosenone CAS NO 37112-31-5

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CAS No.:37112-31-5

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Content:99.90%

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2-Cyclohexen-1-One,2-Methyl-3-(2-Methylpropoxy)-(9Ci) CAS NO 37457-15-1

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CAS No.:37457-15-1

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Content:99.90%

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3-Cyclobutene-1,2-Dione, 3-Chloro-4-(Dimethylamino)- CAS NO 37669-68-4

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CAS No.:37669-68-4

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Content:99.90%

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1,3-Cyclobutanedione, 2,4-Dichloro- CAS NO 37873-66-8

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CAS No.:37873-66-8

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3-Buten-2-One, 4-(Ethylmethylamino)- (9Ci) CAS NO 37993-49-0

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CAS No.:37993-49-0

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Content:99.90%

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2,6-Octanedione CAS NO 38275-04-6

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CAS No.:38275-04-6

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Content:99.90%

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1,12-Cyclodocosanedione CAS NO 38300-52-6

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CAS No.:38300-52-6

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Content:99.90%

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