| Weight | 122.167 g/mol |
|---|---|
| Formula | C8H10O |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
2,3-DIMETHYLPHENOL (526-75-0, 1300-71-6)
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- Diastereoselective Aldol Reaction with an Acetate Enolate: 2,6-Bis(2-isopropylphenyl)-3,5-dimethylphenol as an Extremely Effective Chiral Auxiliary (Angewandte Chemie, 1998)
- Direct hydrodeoxygenation and hydrogenation of 2,6- and 3,5-dimethylphenol over sulphided CoMo catalyst (Applied Catalysis A-general, 1994)
- Perjodatoxydation von Phenolen. VII. 2,6-Dimethylphenol sowie 2,4,6- und 2,3,5-Trimethylphenol. (Acta Chemica Scandinavica, 1960)
- Synthesis of ,-bis(2,6-dimethylphenol)-poly(2,6-dimethyl-1,4-phenylene oxide) by phase transfer catalyzed polymerization of 4-bromo-2,6-dimethylphenol in the presence of 2,2-di(4-hydroxy-3,5-dimethylphenyl)propane (Polymer Bulletin, 1990)
- 2,6-Bis(2-alkylphenyl)-3,5-dimethylphenol as a New Chiral Phenol with C2-Symmetry. Application to the Asymmetric Alkylation of Aldehydes (Journal of Organic Chemistry, 1997)
- Solubility of 2,5-dimethylphenol and 3,4-dimethylphenol in binary solvent mixtures containing alcohols (Fluid Phase Equilibria, 1988)
-
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 -
SMILESCC1=C(C(=CC=C1)O)C
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InChIKeyQWBBPBRQALCEIZ-UHFFFAOYSA-N
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