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.

3-Pentanone CAS NO 96-22-0

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CAS No.:96-22-0

Grade:Pharmacy Grade

Content:99.90%

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3-Methyl-1-Penten-3-Ol CAS NO 918-85-4

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CAS No.:918-85-4

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Content:99.90%

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6-Heptyn-2-One (7Ci,8Ci,9Ci) CAS NO 928-39-2

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CAS No.:928-39-2

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4-Cyclopentene-1,3-Dione CAS NO 930-60-9

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CAS No.:930-60-9

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Content:99.90%

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2-(Hydroxymethyl)Cyclopent-2-Enone CAS NO 930-91-6

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CAS No.:930-91-6

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Content:99.90%

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2-Chloro-3-Hydroxycyclohex-2-En-1-One, 98% CAS NO 932-23-0

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CAS No.:932-23-0

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Ethanone, 2-Chloro-1-Cyclopentyl- (9Ci) CAS NO 932-28-5

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CAS No.:932-28-5

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Tetramethyl-1,3-Cyclobutanedione CAS NO 933-52-8

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CAS No.:933-52-8

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Content:99.90%

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