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-Pentanone, 3,4-Dihydroxy-3-Methyl-, (R*,R*)- (9Ci) CAS NO 53689-01-3

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CAS No.:53689-01-3

Grade:Pharmacy Grade

Content:99.90%

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2-Pentanone, 3,4-Dihydroxy-3-Methyl-, (R*,S*)- (9Ci) CAS NO 53689-02-4

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CAS No.:53689-02-4

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2-Cyclohexen-1-One, 4-Butyl-3-Methoxy- CAS NO 53690-84-9

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CAS No.:53690-84-9

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2-Cyclohexen-1-One,3-Methoxy-2-Propyl-(9Ci) CAS NO 53690-85-0

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CAS No.:53690-85-0

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Bicyclo[4.1.0]Hept-3-Ene-2,5-Dione CAS NO 53735-22-1

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CAS No.:53735-22-1

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Diallyl Ketone CAS NO 53859-89-5

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CAS No.:53859-89-5

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2,3,3,4-Tetramethylcyclobutanone CAS NO 53907-62-3

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CAS No.:53907-62-3

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Content:99.90%

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1,5,6,6-Tetramethoxy-3-Hexanone CAS NO 53914-29-7

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CAS No.:53914-29-7

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Content:99.90%

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