Cyclopentene

It has few applications, and thus is mainly used as a minor component of gasoline, present in concentrations of less than 1%.

Cyclopentene was first prepared by Carl Gärtner in 1893 from iodocyclopentane with potassium hydroxide.

[3] Cyclopentene is produced industrially in large amounts by steam cracking of naphtha.

The polymerization of cyclopentene by Ziegler-Natta catalysts yields 1,3-linkages, not the more typical 1,2-linked polymer.

[7] Palladium-catalyzed hydrocarboxylation of cyclopentene gives cyclopentanecarboxylic acid:[8] This article about a hydrocarbon is a stub.

Cyclopentene
Cyclopentene
Ball-and-stick model of cyclopentene
Ball-and-stick model of cyclopentene
Space-filling model of cyclopentene
Space-filling model of cyclopentene
NFPA 704 four-colored diamond Health 1: Exposure would cause irritation but only minor residual injury. E.g. turpentine Flammability 3: Liquids and solids that can be ignited under almost all ambient temperature conditions. Flash point between 23 and 38 °C (73 and 100 °F). E.g. gasoline Instability 1: Normally stable, but can become unstable at elevated temperatures and pressures. E.g. calcium Special hazards (white): no code