| Weight | 86.09 g/mol |
|---|---|
| Formula | C4H6O2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
3-Oxotetrahydrofuran (22929-52-8)
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- Kinetic evidence for the coexistence of zwitterionic (T+/-), neutral (T0) and anionic (T-) intermediates during rearrangement of S-(2-oxotetrahydrofuran-3-yl)-N-(4-methoxyphenyl)isothiuronium bromide to 5-(2-hydroxyethyl)-2-(4-methoxyphenylimino)-1,3-thiazolidin-4-one. (Journal of Organic Chemistry, 2010)
- Parallel solution phase synthesis of benzyl (3S,4E)-4-[(arylamino)methylidene]-5-oxotetrahydrofuran-3-ylcarbamates (Arkivoc, 2003)
- Process Research on [(2S)-(3-Fluorophenyl)-(1S)-(5-oxotetrahydrofuran- 2-yl)ethyl]carbamic Acid tert-Butyl Ester, a Lactone Intermediate for an Aspartyl Protease Inhibitor (Organic Process Research & Development, 2004)
- 4-Methylene-2-octyl-5-oxotetrahydrofuran-3-carboxylic Acid (C75), an Inhibitor of Fatty-acid Synthase, Suppresses the Mitochondrial Fatty Acid Synthesis Pathway and Impairs Mitochondrial Function (Journal of Biological Chemistry, 2014)
- Synthesis of spirolactones by 1,3-dipolar cycloadditions to methyl (S)-3-[(E)-cyanomethylidene]-2-oxotetrahydrofuran-5-carboxylate (Journal of Heterocyclic Chemistry, 2002)
- STEREOSELECTIVE SYNTHESIS OF 5-SUBSTITUTED 2-ALLYL-3-OXOTETRAHYDROFURAN-2-CARBOXYLATES USING RHODIUM(II)-CATALYZED OXONIUM YLIDE FORMATION-12,3] SHIFT (Heterocycles, 2009)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1COCC1=O
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InChIKeyJLPJFSCQKHRSQR-UHFFFAOYSA-N
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