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, 4-(Dimethylamino)-4-(3-Methoxyphenyl)- CAS NO 65618-98-6

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CAS No.:65618-98-6

Grade:Pharmacy Grade

Content:99.90%

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2-Cyclohexen-1-One, 5-Ethynyl-2-Methyl- (9Ci) CAS NO 65648-52-4

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CAS No.:65648-52-4

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Content:99.90%

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Ethanone,1-(1-Ethynylcyclopentyl)- CAS NO 65691-71-6

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CAS No.:65691-71-6

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Content:99.90%

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(R)-5-Hydroxy-2-Hexanone CAS NO 65709-73-1

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CAS No.:65709-73-1

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Content:99.90%

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6-Phenoxy-Hexan-2-One CAS NO 65851-20-9

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CAS No.:65851-20-9

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Content:99.90%

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3-Buten-2-One, 3-Ethoxy- (9Ci) CAS NO 65915-73-3

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CAS No.:65915-73-3

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Content:99.90%

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Cyclobutanone, 3-Ethenyl- CAS NO 66166-61-8

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CAS No.:66166-61-8

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Content:99.90%

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Ethanone, 1-(2-Bromocyclopropyl)-, trans- (9Ci) CAS NO 66236-38-2

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CAS No.:66236-38-2

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Content:99.90%

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