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, 4-Hydroxy-4-Methoxy- (9Ci) CAS NO 131023-29-5

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CAS No.:131023-29-5

Grade:Pharmacy Grade

Content:99.90%

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Ethanone, 1-(5-Methyl-1,2,4-Trioxolan-3-Yl)- (9Ci) CAS NO 131250-91-4

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CAS No.:131250-91-4

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Content:99.90%

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2-Butanone, 4-Bicyclo[1.1.1]Pent-2-Yl- (9Ci) CAS NO 131322-95-7

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CAS No.:131322-95-7

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Content:99.90%

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3-Buten-1-One, 2-Chloro-1-Cyclobutyl-2,3-Dimethyl- (9Ci) CAS NO 131353-07-6

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CAS No.:131353-07-6

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Content:99.90%

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Ethanone, 1-(2-Ethenyl-2-Methylcyclobutyl)- (9Ci) CAS NO 131510-64-0

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CAS No.:131510-64-0

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Content:99.90%

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Ethanone, 1-[2-Methyl-2-(1-Methylethenyl)Cyclobutyl]- (9Ci) CAS NO 131510-65-1

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CAS No.:131510-65-1

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Content:99.90%

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1-(1-Azepanyl)-2-Bromo-1-Propanone CAS NO 131580-51-3

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CAS No.:131580-51-3

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Content:99.90%

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(E)-5[(4-Chlorophenyl)Methylene]-2,2-Dimethylcyclopentanone CAS NO 131984-21-9

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CAS No.:131984-21-9

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Content:99.90%

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