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.

5-Tridecanone CAS NO 30692-16-1

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CAS No.:30692-16-1

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Content:99.90%

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Ethanone, 1-(1-Hydroxy-1H-1,2,3-Triazol-5-Yl)- (9Ci) CAS NO 207860-65-9

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CAS No.:207860-65-9

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4-Cycloheptene-1,3-Dione,6-(1-Methylethyl)-(9Ci) CAS NO 207925-56-2

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CAS No.:207925-56-2

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2-Propanone, 1-Hydroxy-1-(2-Pyrrolidinyl)- (9Ci) CAS NO 208102-58-3

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CAS No.:208102-58-3

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2-Benzyloxymethyl-Cyclobutanone CAS NO 294868-56-7

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CAS No.:294868-56-7

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4-Hexen-2-One, 4-Methyl-, (4E)- (9Ci) CAS NO 294887-83-5

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CAS No.:294887-83-5

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3-Buten-2-One, 4-(Methoxymethoxy)-3-Methyl-, (3E)- (9Ci) CAS NO 297163-08-7

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CAS No.:297163-08-7

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2-Cyclopenten-1-One,5-Ethylidene-3-Methoxy-4-Methylene-(9Ci) CAS NO 297753-36-7

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CAS No.:297753-36-7

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