Weight | 70.091 g/mol |
---|---|
Formula | C4H6O |
Hydrogen Acceptors | 1 |
Hydrogen Donors | 0 |
Aromatic Rings | 0 |
Rotatable Bonds | 0 |
2,5-DIHYDROFURAN (1708-29-8)
Score:
#2334 in Physics
,
#7171 in Chemistry
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- RingPuckering Motion of 2,5Dihydrofuran (Journal of Chemical Physics, 1967)
- Preparation of Cis- and Trans 2,5-Dimethoxy-2-(acetamidomethyl)-2,5-dihydrofuran, of Cis- and Trans 2,5-Dimethoxy-2-(acetamidomethyl)-tetrahydrofuran and of 1-Phenyl-2-(acetamidomethyl)-pyrrole. (Acta Chemica Scandinavica, 1952)
- Focused Microwave-Assisted Synthesis of 2,5-Dihydrofuran Derivatives as Electron Acceptors for Highly Efficient Nonlinear Optical Chromophores (Advanced Materials, 2003)
- CONSTRUCTION OF A MOLECULAR BEAM FOURIER TRANSFORM MICROWAVE SPECTROMETER USED TO STUDY THE 2,5-DIHYDROFURAN-ARGON VAN DER WAALS COMPLEX (Chemical Physics, 1997)
- Chemical and enzymatic syntheses of 6-deoxyhexoses. Conversion to 2,5-dimethyl-4-hydroxy-2,3-dihydrofuran-3-one (Furaneol) and analogs (Journal of Organic Chemistry, 1983)
- Self-supported paired electrosynthesis of 2,5-dimethoxy-2,5-dihydrofuran using a thin layer flow cell without intentionally added supporting electrolyte (Electrochemistry Communications, 2005)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1C=CCO1
-
InChIKeyARGCQEVBJHPOGB-UHFFFAOYSA-N
- Pubchem - 2,5-DIHYDROFURAN
- Wikipedia - 2,5-Dihydrofuran
2,5-Dihydrofuran is the organic compound classified as a monounsaturated derivative of furan. It is a colorless, volatile liquid. It can be produced by the rearrangement of the epoxide of butadiene.
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