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.

2-Pentacosanone CAS NO 75207-54-4

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CAS No.:75207-54-4

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Content:99.90%

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Ethanone, 1-(1,5-Cyclohexadien-1-Yl)- (9Ci) CAS NO 75250-64-5

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CAS No.:75250-64-5

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3-Bromo-1,1-Dimethoxy-2-Propanone CAS NO 75271-94-2

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CAS No.:75271-94-2

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2,4,4,5-Tetramethyl-3-(3-Oxo-1-Butenyl)-2-Cyclohexen-1-One CAS NO 75332-28-4

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CAS No.:75332-28-4

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(R)-4-Methylcyclohex-2-Enone CAS NO 75337-05-2

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CAS No.:75337-05-2

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3-[3-(1,3-Dioxolan-2-Yl)Propyl]Cyclohexanone CAS NO 75506-74-0

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CAS No.:75506-74-0

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2-Propanone, 1-Bromo-3-Methoxy- CAS NO 75522-04-2

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CAS No.:75522-04-2

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5-Nonen-8-Yn-2-One, (E)- (9Ci) CAS NO 75606-72-3

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CAS No.:75606-72-3

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