| Weight | 136.194 g/mol |
|---|---|
| Formula | C9H12O |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
2,4,6-TRIMETHYLPHENOL (527-60-6)
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- Inhibition of humic substances mediated photooxygenation of furfuryl alcohol by 2,4,6-trimethylphenol. Evidence for reactivity of the phenol with humic triplet excited states. (Environmental Science & Technology, 2007)
- Aerobic oxidation of 2,3,6-trimethylphenol to trimethyl-1,4-benzoquinone with copper(II) chloride as catalyst in ionic liquid and structure of the active species. (Journal of the American Chemical Society, 2004)
- Photo-oxidation of 2,4,6-trimethylphenol in aqueous laboratory solutions and natural waters : kinetics of reaction with singlet oxygen (Journal of Photochemistry and Photobiology A-chemistry, 1994)
- Gas-phase acidities and O-H bond dissociation enthalpies of phenol, 3-methylphenol, 2,4,6-trimethylphenol, and ethanoic acid. (Journal of Physical Chemistry A, 2006)
- A novel oxygenation of 2,4,6-trimethylphenol to 3,5-dimethyl-4-hydroxybenzaldehyde by dioxygen with copper(II)-amine complex catalyst (Tetrahedron Letters, 1990)
- Perjodatoxydation von Phenolen. VII. 2,6-Dimethylphenol sowie 2,4,6- und 2,3,5-Trimethylphenol. (Acta Chemica Scandinavica, 1960)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H315: Causes skin irritation
Warning Skin corrosion/irritation - Category 2 - H410: Very toxic to aquatic life with long lasting effects
Warning Hazardous to the aquatic environment, long-term hazard - Category 1 -
SMILESCC1=CC(=C(C(=C1)C)O)C
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InChIKeyBPRYUXCVCCNUFE-UHFFFAOYSA-N
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2,4,6-TRIMETHYLPHENOL
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