TCI C0466 Cycloheptanone (CAS 502-42-1) is a seven-membered cyclic ketone valued as a flexible building block in organic synthesis. It readily undergoes nucleophilic addition, aldol condensation, alpha-alkylation, and enamine or enol ether formation. The compound also serves as a precursor to cycloheptanol, oximes, and related seven-membered ring derivatives used in natural product synthesis. Available in 25 mL, 100 mL, and 500 mL packs, this flammable liquid should be handled in a fume hood and stored tightly closed in a cool, well-ventilated place.
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- Tanino et al. (2002). Stereoselective Synthesis of Cycloheptanone Derivatives via an Intermolecular [5 + 2] Cycloaddition Reaction.. ChemInform doi:10.1002/chin.200244096
- Banwell et al. (2005). The Synthesis of E‐2‐(Bromomethylene)cyclohexanone and E‐2‐(Bromomethylene)cycloheptanone.. ChemInform doi:10.1002/chin.200530059
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