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-Methyl-3-Hexanone CAS NO 7379-12-6

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CAS No.:7379-12-6

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Content:99.90%

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Ethanone, 2-Chloro-1-Cyclopropyl- (9Ci) CAS NO 7379-14-8

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CAS No.:7379-14-8

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2-(1-Oxopropyl)Cyclopentan-1-One CAS NO 7391-48-2

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CAS No.:7391-48-2

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3,5-Dimethyl-4-Octanone CAS NO 7335-17-3

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CAS No.:7335-17-3

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3,5-Heptanedione CAS NO 7424-54-6

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CAS No.:7424-54-6

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2-Methoxycyclohexanone CAS NO 7429-44-9

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CAS No.:7429-44-9

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Content:99.90%

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Thiocamphor CAS NO 7519-74-6

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CAS No.:7519-74-6

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Content:99.90%

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1,3-Dibromo-1-Propanone CAS NO 7623-16-7

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CAS No.:7623-16-7

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Content:99.90%

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