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-Benzylcyclopentanone CAS NO 85163-16-2

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CAS No.:85163-16-2

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Content:99.90%

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2-Methoxy-5,5-Dimethylcyclohex-2-Enone CAS NO 85312-29-4

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CAS No.:85312-29-4

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trans-3A-Methylperhydroazulen-4(1H)-One CAS NO 85318-94-1

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CAS No.:85318-94-1

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Content:99.90%

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3-Benzylcyclohexanone CAS NO 85450-51-7

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CAS No.:85450-51-7

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Content:99.90%

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4-Hexen-2-One, 4-Methyl-, (4Z)- (9Ci) CAS NO 85470-78-6

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CAS No.:85470-78-6

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Ethanone, 1-Bicyclo[2.1.1]Hex-5-Yl-, (1Alpha,4Alpha,5Alpha)- (9Ci) CAS NO 85439-92-5

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CAS No.:85439-92-5

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7-Hydroxy-6-Dodecanone CAS NO 6790-20-1

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CAS No.:6790-20-1

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6-Tetradecanone CAS NO 6836-42-6

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CAS No.:6836-42-6

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Content:99.90%

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