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.

4,4-Dimethyl-5-(Dimethylamino)-1-(3-Methylcyclohexyl)-1-Pentanone CAS NO 3853-21-2

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CAS No.:3853-21-2

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Content:99.90%

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2-Acetyl-1,3-Cyclopentanedione CAS NO 3859-39-0

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CAS No.:3859-39-0

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Content:99.90%

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(5Z,9Z,13E)-6,10,14,18-Tetramethylnonadeca-5,9,13,17-Tetraen-2-One CAS NO 3879-24-1

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CAS No.:3879-24-1

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Acetone-2-13C CAS NO 3881-06-9

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CAS No.:3881-06-9

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Content:99.90%

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2-Cyclopenten-1-One,3-Methoxy-2-Methyl-(7Ci,8Ci,9Ci) CAS NO 3883-56-5

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CAS No.:3883-56-5

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2,2-Dimethyl-1,3-Cyclopentanedione CAS NO 3883-58-7

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CAS No.:3883-58-7

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Content:99.90%

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1,1-Dichloro-1-Fluoroacetone CAS NO 3929-28-0

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CAS No.:3929-28-0

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Content:99.90%

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3-Hydroxycyclohex-2-En-1-One CAS NO 30182-67-3

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CAS No.:30182-67-3

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Content:99.90%

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