| Weight | 122.167 g/mol |
|---|---|
| Formula | C8H10O |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
2,6-DIMETHYLPHENOL (25134-01-4, 576-26-1)
2,6-xylenol
Score:
#1820 in Chemistry
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- Polymerization by Oxidative Coupling. The Function of Copper in the Oxidation of 2,6-Dimethylphenol (Journal of Organic Chemistry, 1966)
- Enzymatic Oxidative Polymerization of 2,6-Dimethylphenol (Macromolecules, 1996)
- Ab initio calculations on 2,6-dimethylphenol and 4-(2,6-dimethylphenoxy)-2,6-dimethylphenol. Evidence of an important role for the phenoxonium cation in the copper-catalyzed oxidative phenol coupling reaction (Journal of the American Chemical Society, 1997)
- The kinetics of the oxidative polymerization of 2.6-xylenol with a copper-amine complex (Macromolecular Chemistry and Physics, 1972)
- Ferrospinels based on Co and Ni prepared via a low temperature route as efficient catalysts for the selective synthesis of o-cresol and 2,6-xylenol from phenol and methanol (Journal of Molecular Catalysis A-chemical, 2002)
- Oxidative Polymerization of 2,6-Dimethylphenol to Form Poly(2,6-dimethyl-1,4-phenyleneoxide) in Water (Angewandte Chemie, 2004)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H301: Toxic if swallowed
Danger Acute toxicity, oral - Category 3 - H314: Causes severe skin burns and eye damage
Danger Skin corrosion/irritation - Category 1A, B, C - H370: Causes damage to organs
Danger Specific target organ toxicity, single exposure - Category 1 - H401: Toxic to aquatic life
Hazardous to the aquatic environment, acute hazard - Category 2 - 2,6-xylenol
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SMILESCC1=C(C(=CC=C1)C)O
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InChIKeyNXXYKOUNUYWIHA-UHFFFAOYSA-N
- Pubchem - 2,6-DIMETHYLPHENOL
- Wikipedia - 2,6-Xylenol
2,6-Xylenol is a chemical compound which is one of the six isomers of xylenol. It is also commonly known as 2,6-dimethylphenol (DMP). A known application of DMP is in the synthesis of Mexiletine.
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2,6-DIMETHYLPHENOL
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