Weight | 122.167 g/mol |
---|---|
Formula | C8H10O |
Hydrogen Acceptors | 1 |
Hydrogen Donors | 1 |
Aromatic Rings | 1 |
Rotatable Bonds | 0 |
2,5-DIMETHYLPHENOL (95-87-4)
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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)
- Regiocontrolled Oxidative Coupling Polycondensation of 2,5-Dimethylphenol Induced by Mesoporous Interior (Macromolecules, 2004)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H301: Toxic if swallowed
Danger Acute toxicity, oral - Category 3 - H302: Harmful if swallowed
Warning Acute toxicity, oral - Category 4 - H314: Causes severe skin burns and eye damage
Danger Skin corrosion/irritation - Category 1A, B, C - H411: Toxic to aquatic life with long lasting effects
Hazardous to the aquatic environment, long-term hazard - Category 2 -
SMILESCC1=CC(=C(C=C1)C)O
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InChIKeyNKTOLZVEWDHZMU-UHFFFAOYSA-N
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