| Weight | 150.221 g/mol |
|---|---|
| Formula | C10H14O |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
3-tert-Butylphenol (585-34-2)
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- Reactions of 2,2-Methylenebis(4-chloro-6-isopropyl-3-methylphenol) and 2,2-Ethylidenebis(4,6-di-tert-butylphenol) with MgnBu2: Efficient Catalysts for Ring-Opening Polymerization of -Caprolactone and l-Lactide (Macromolecules, 2004)
- Calixarenes. 3. Preparation of the 2,4-dinitrophenyl and camphorsulfonyl derivatives of the calix[8]arene from p-tert-butylphenol (Journal of Organic Chemistry, 1979)
- High-pressure vapor-liquid equilibria for CO[sub 2] + benzonitrile, CO[sub 2] + benzyl alcohol, CO[sub 2] + 2-tert-butylphenol, CO[sub 2] + methoxybenzene, and CO[sub 2] + 1,2,3,4-Tetrahydronaphthalene at temperatures between 313 and 393 K and pressures up to 20 MPa (Journal of Chemical & Engineering Data, 1993)
- Oxidation of 2,6-di-tert-butylphenol with tert-butylhydroperoxide catalyzed by cobalt(II) phthalocyanine tetrasulfonate in a methanolwater mixture and formation of an unusual product 4,4-dihydroxy-3,3,5,5-tetra-tert-butylbiphenyl (Journal of Molecular Catalysis A-chemical, 2005)
- Aquatic Toxicity of Four Alkylphenols (3-tert-Butylphenol, 2-Isopropylphenol, 3-Isopropylphenol, and 4-Isopropylphenol) and Their Binary Mixtures to Microbes, Invertebrates, and Fish (Environmental Toxicology, 2004)
- Base-catalyzed oxygenation of tert-butylated phenols. 3. Base-catalyzed reaction of peroxyquinols derived from oxygenation of 2,6-di-tert-butylphenols and mechanism of regioselective formation of epoxy-o-quinol from 2,4,6-tri-tert-butylphenol (Journal of Organic Chemistry, 1979)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC(C)(C)C1=CC(=CC=C1)O
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InChIKeyCYEKUDPFXBLGHH-UHFFFAOYSA-N
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