| Weight | 86.134 g/mol |
|---|---|
| Formula | C5H10O |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
TETRAHYDROPYRAN (142-68-7)
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#4346 in Chemistry
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- Synthetic routes to tetrahydrofuran, tetrahydropyran, and spiroketal units of polyether antibiotics and a survey of spiroketals of other natural products (Tetrahedron, 1987)
- Activation of 6-endo over 5-exo hydroxy epoxide openings. Stereoselective and ring selective synthesis of tetrahydrofuran and tetrahydropyran systems (Journal of the American Chemical Society, 1989)
- Combining pot, atom and step economy (PASE) in organic synthesis. Synthesis of tetrahydropyran-4-ones (Green Chemistry, 2007)
- Activation of 7-endo over 6-exo epoxide openings. Synthesis of oxepane and tetrahydropyran systems (Journal of the American Chemical Society, 1989)
- Mathematical Representation of Thermodynamic Properties. Carbazole Solubilities in Binary Alkane + Dibutyl Ether and Alkane + Tetrahydropyran Solvent Mixtures (Physics and Chemistry of Liquids, 1991)
- Chemoselective Hydrogenolysis of Tetrahydropyran2methanol to 1,6Hexanediol over RheniumModified CarbonSupported Rhodium Catalysts (Chemcatchem, 2010)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H225: Highly Flammable liquid and vapor
Danger Flammable liquids - Category 2 -
SMILESC1CCOCC1
-
InChIKeyDHXVGJBLRPWPCS-UHFFFAOYSA-N
- Pubchem - TETRAHYDROPYRAN
- Wikipedia - tetrahydropyran
Tetrahydropyran (THP) is the organic compound consisting of a saturated six-membered ring containing five carbon atoms and one oxygen atom. It is named by reference to pyran, which contains two double bonds, and may be produced from it by adding four hydrogens. In 2013, its preferred IUPAC name was established as oxane.
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TETRAHYDROPYRAN
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