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-Propanone, 1-(2,5-Dihydro-2-Furanyl)-, (R)- (9Ci) CAS NO 124031-52-3

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CAS No.:124031-52-3

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Content:99.90%

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8-(4-Chlorophenoxy)Oct-1-En-2-Ol CAS NO 124083-15-4

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CAS No.:124083-15-4

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Content:99.90%

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3-Pentanone, 4-Hydroxy-2,2-Dimethyl-, (R)- (9Ci) CAS NO 124089-61-8

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CAS No.:124089-61-8

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3-Penten-2-One, 4-(2-Propenylamino)- (9Ci) CAS NO 124747-44-0

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CAS No.:124747-44-0

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Content:99.90%

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2-Acetyl-Cyclohexanone CAS NO 125117-37-5

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CAS No.:125117-37-5

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Content:99.90%

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Ethanone, 1-[(1R,2R)-1,2-Dihydroxy-3-Cyclohexen-1-Yl]-, Rel- (9Ci) CAS NO 125229-00-7

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CAS No.:125229-00-7

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Content:99.90%

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Ethanone, 1-(1,2-Dihydroxy-3-Cyclohexen-1-Yl)-, cis- (9Ci) CAS NO 125229-01-8

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CAS No.:125229-01-8

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Content:99.90%

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3-Hydroxy-4,4-Dimethyl-3-(1-Methyl-3-Oxobut-1-Enyl)Cycloheptanone CAS NO 125257-74-1

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CAS No.:125257-74-1

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Content:99.90%

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