| Weight | 116.16 g/mol |
|---|---|
| Formula | C6H12O2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 1 |
TETRAHYDROPYRAN-2-METHANOL (100-72-1)
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- Chemoselective Hydrogenolysis of Tetrahydropyran2methanol to 1,6Hexanediol over RheniumModified CarbonSupported Rhodium Catalysts (Chemcatchem, 2010)
- Production of 1,6-hexanediol from tetrahydropyran-2-methanol by dehydrationhydration and hydrogenation (Green Chemistry, 2017)
- The Hydrogenation of Pyran Derivatives. IV. The Skeletal Rearrangement in the Gas-phase Dehydration of Tetrahydropyran-2-methanol (Bulletin of the Chemical Society of Japan, 1968)
- Selectivity enhancement of PPL-catalyzed resolution by enzyme fractionation and medium engineering: Syntheses of both enantiomers of tetrahydropyran-2-methanol (Enzyme and Microbial Technology, 1996)
- Effect of carbon supports on RhRe bifunctional catalysts for selective hydrogenolysis of tetrahydropyran-2-methanol (Catalysis Science & Technology, 2016)
- Multinuclear magnetic resonance study of the complexation of lanthanide(III) cations with tetrahydropyran-2-methanol (Journal of The Chemical Society-dalton Transactions, 1992)
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Predict GHS Hazards for Any Chemical in silico.
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SMILESC1CCOC(C1)CO
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InChIKeyROTONRWJLXYJBD-UHFFFAOYSA-N
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TETRAHYDROPYRAN-2-METHANOL
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