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.

Ethanone, 1-(1,3,3-Trimethyl-2-Aziridinyl)- (9Ci) CAS NO 104547-67-3

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CAS No.:104547-67-3

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Content:99.90%

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2-Heptanone, 3-Ethenylidene- (9Ci) CAS NO 104550-70-1

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CAS No.:104550-70-1

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4-(Diethylamino)Cyclohexanone CAS NO 104618-24-8

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CAS No.:104618-24-8

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Octahydro-1,4:5,8-Dimethanonaphthalen-2(1H)-One CAS NO 104832-30-6

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CAS No.:104832-30-6

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Hexa-1,5-Diene-3,4-Dione CAS NO 104910-78-3

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CAS No.:104910-78-3

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Ethanone, 1-Bicyclo[2.1.0]Pent-2-Yl-, (1Alpha,2Alpha,4Alpha)- (9Ci) CAS NO 104951-19-1

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CAS No.:104951-19-1

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Ethanone, 1-Bicyclo[2.1.0]Pent-2-Yl-, (1Alpha,2Beta,4Alpha)- (9Ci) CAS NO 105017-00-3

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CAS No.:105017-00-3

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Content:99.90%

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1-Butanone, 1-(5-Bromo-2-Hydroxyphenyl)- CAS NO 105211-80-1

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CAS No.:105211-80-1

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