Cycloheptanone TCI C0466

Chemical Identity

Other names: Suberone
CAS No.: 502-42-1
Formula: C7H12O
Molecular weight: 112.17 g/mol
Purity: >98.0%(GC)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: cycloheptanone
SMILES: C1CCCC(=O)CC1
InChIKey: CGZZMOTZOONQIA-UHFFFAOYSA-N
MDL: MDL00004159
PubChem: CID 10400

Rp 1.696.800,00

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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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Mahran et al. (2026). Synthesis and antimicrobial activities of novel polynuclear heterocyclic compounds derived from 8-fluoro-benzosuberone and cycloheptanone. Afinidad. Journal of Chemical Engineering Theoretical and Applied Chemistry doi:10.55815/980000013902
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

References were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.