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-Ethyl-1,2,4-Cyclopentanetrione CAS NO 4505-53-7

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CAS No.:4505-53-7

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Content:99.90%

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5-Methylcyclopentane-1,2,4-Trione CAS NO 4505-54-8

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CAS No.:4505-54-8

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Content:99.90%

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2,2-Dimethylcyclopentanone CAS NO 4541-32-6

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CAS No.:4541-32-6

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Content:99.90%

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2,2,5,5-Tetramethylcyclopentanone CAS NO 4541-35-9

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CAS No.:4541-35-9

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Content:99.90%

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1-(1-Pyrrolidyl)-1-Propanone CAS NO 4553-05-3

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CAS No.:4553-05-3

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Content:99.90%

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(R)-6-(Isopropyl)-3-Methylcyclohex-2-En-1-One CAS NO 4573-50-6

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CAS No.:4573-50-6

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Content:99.90%

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2-tert-Butylcyclobutanone CAS NO 4579-31-1

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CAS No.:4579-31-1

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Content:99.90%

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1-Piperidin-1-Ylhexadecan-1-One CAS NO 4629-02-1

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CAS No.:4629-02-1

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Content:99.90%

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