2,5-Dihydrofuran is an organic compound classified as a monounsaturated derivative of furan. It is a colorless, volatile liquid. It can be produced from the acid-catalyzed rearrangement 1‑butene 3,4‑epoxide.[2]
Names | |||
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Preferred IUPAC name 2,5-Dihydrofuran | |||
Identifiers | |||
3D model (JSmol) | |||
ChEMBL | |||
ChemSpider | |||
ECHA InfoCard | 100.015.416 | ||
PubChem CID | |||
UNII | |||
CompTox Dashboard (EPA) | |||
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Properties | |||
C4H6O | |||
Molar mass | 70.091 g·mol−1 | ||
Density | 0.9461 g cm−3 [1] | ||
Melting point | −86 °C (−123 °F; 187 K) | ||
Boiling point | 67.4 °C (153.3 °F; 340.5 K)[1] | ||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). |
References edit
- ^ a b Paul; et al. (1950). Bulletin de la Société Chimique de France: 668–.
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: CS1 maint: untitled periodical (link) - ^ G. Wytze Meindersma, Matthias Maase and André B. Haan "Ionic Liquids" in Ullmann's Encyclopedia Of Industrial Chemistry 2007, Wiley-VCH, Weinheim. doi:10.1002/14356007.l14_l01
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