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.

3-Octanone, 4-Chloro-5-Methyl- CAS NO 343270-33-7

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CAS No.:343270-33-7

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Content:99.90%

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2-Propanone, 1-(2-Ethyl-2-Hydroxycyclopropyl)- (9Ci) CAS NO 343313-30-4

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CAS No.:343313-30-4

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2,4,7-Cyclononatrien-1-One, 5-Methyl- (9Ci) CAS NO 343863-90-1

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CAS No.:343863-90-1

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Ethanone, 1-[2-(Acetyloxy)Cyclopentyl]- (9Ci) CAS NO 343868-35-9

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CAS No.:343868-35-9

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2-Pentanone, 5,5-Dihydroxy- (9Ci) CAS NO 373380-20-2

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CAS No.:373380-20-2

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Cyclopentanone, 3-Butyl-4-Methyl-, (3R,4R)-Rel- (9Ci) CAS NO 373354-63-3

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CAS No.:373354-63-3

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2-Hexanone, 4-Ethyl-5-Methyl-, (4S)- (9Ci) CAS NO 376355-65-6

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CAS No.:376355-65-6

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5-Octene-3,7-Diyn-2-One, (5Z)- (9Ci) CAS NO 377078-02-9

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CAS No.:377078-02-9

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Content:99.90%

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