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-Cyclopentyl-Pentan-1-One CAS NO 6636-80-2

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CAS No.:6636-80-2

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Content:99.90%

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(R)-(+)-3-Methylcyclopentanone CAS NO 6672-30-6

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CAS No.:6672-30-6

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1-Cyclobutylpropan-1-One CAS NO 6704-17-2

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CAS No.:6704-17-2

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1-Cyclopropyl-1-Propanone CAS NO 6704-19-4

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CAS No.:6704-19-4

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Content:99.90%

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3-Oxetanone CAS NO 6704-31-0

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CAS No.:6704-31-0

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Cyclopropyl Propyl Ketone CAS NO 6705-46-0

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CAS No.:6705-46-0

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Hept-5-En-2-One CAS NO 6714-00-7

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CAS No.:6714-00-7

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Content:99.90%

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4,4,5-Trimethylhex-5-En-3-One CAS NO 6948-98-7

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CAS No.:6948-98-7

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