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Names | |||
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Preferred IUPAC name
Cyclobutene | |||
Identifiers | |||
3D model (JSmol)
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ChEBI | |||
ChemSpider | |||
ECHA InfoCard | 100.011.360 | ||
EC Number |
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PubChem CID
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CompTox Dashboard (EPA)
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Properties | |||
C4H6 | |||
Molar mass | 54.092 g·mol−1 | ||
Appearance | Colorless gas | ||
Density | 0.733 g/cm3 | ||
Boiling point | 2 °C (36 °F; 275 K)[1] | ||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Cyclobutene is an organic compound with the chemical formula C4H6. It is a cycloalkene. It is a colorless gas that easily condenses. It is of interest in research but currently has no practical applications. A modern synthesis involves the 2-step dehydration of cyclobutanol.[1] The compound was first prepared by thermolysis of the ammonium salt [C4H7N(CH3)3]OH (cyclobutyltrimethylammonium hydroxide).[2]
Cyclobutene thermally isomerizes to 1,3-butadiene. This strongly exothermic reaction reflects the dominance of ring strain. In contrast, the corresponding equilibrium for hexafluorocyclobutene disfavors hexafluorobutadiene.[3]