Odrónione

Odrónione is a synthetic organic compound classified as a bicyclic monoketone. In chemical literature it is commonly used as a model substrate for exploring cyclization processes and carbonyl reactivity. The defined molecular formula is C12H14O, with a molecular weight of 178.24 g/mol.

It comprises a fused ring system that combines a six-membered ring with a five-membered ring, bearing a single ketone functional group. The ketone participates in typical carbonyl chemistry and contributes to characteristic spectroscopic features observed in infrared and nuclear magnetic resonance analyses.

Odrónione is described as a colorless to pale-yellow liquid at room temperature. It is soluble in most organic solvents such as ethanol, diethyl ether, and dichloromethane, and is sparingly soluble in water. Its boiling point is estimated around 210°C.

Occurrence and synthesis: Odrónione is not known to occur naturally. It is prepared synthetically by intramolecular cyclization of suitably substituted enones or by oxidation of bicyclic alcohol precursors under mild catalytic conditions.

Applications: In research settings, odrónione serves as a standard substrate for studying cyclization mechanisms, the reactivity of ketone groups under various catalysts, and as a benchmark in spectral analysis.

Safety: Odrónione is a potential eye and skin irritant and should be handled with gloves and eye protection. It is flammable and should be stored away from heat sources and oxidizers.

See also: Ketone, Cyclization, Bicyclic compound.