2-(1-Cyclohexenyl)cyclohexanone (TCI C1160, CAS 1502-22-3) is the self-aldol condensation product of cyclohexanone and contains both a ketone and a cyclic alkene. This dual functionality makes it a useful substrate for annulation reactions and for building polycyclic and terpenoid-like frameworks. It also serves as a convenient test substrate for selective hydrogenation, epoxidation, and enolate chemistry. Supplied as a liquid in 25 mL and 500 mL sizes, it should be handled in a fume hood and stored tightly sealed away from oxidizers and ignition sources.
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- Saha et al. (1998). Cation exchange resin-catalysed esterification of acetic acid with 2-(1-cyclohexenyl)cyclohexanone. Catalysis Letters doi:10.1023/a:1019084901133
- AKIMOVA et al. (1990). ChemInform Abstract: Condensation of Aldehydes and Ketones. Part 24. Synthesis and Reactions of 1,5‐Diketones from 2‐(1‐Cyclohexenyl)cyclohexanone and 2‐Cyclopentylidenecyclopentanone.. ChemInform doi:10.1002/chin.199045080
- Mortko et al. (2003). H-abstraction prevails over α-cleavage in the solution and solid state photochemistry of cis-2,6-di(1-cyclohexenyl)cyclohexanone. Tetrahedron Letters doi:10.1016/s0040-4039(03)01450-3
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