| Weight | 222.328 g/mol |
|---|---|
| Formula | C14H22O2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
3,5-Di-tert-butylcatechol (1020-31-1)
3,5-di-t-butyl catechol
Score:
#38 in Inorganic chemistry
,
#6569 in Chemistry
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- Studies on Aerobic Reactions of Ammonia/3,5-Di-tert-butylcatechol Schiff-Base Condensation Products with Copper, Copper(I), and Copper(II). Strong Copper(II)Radical Ferromagnetic Exchange and Observations on a Unique NN Coupling Reaction (Inorganic Chemistry, 1996)
- Synthetic, structural, and physical studies of titanium complexes of catechol and 3,5-di-tert-butylcatechol (Inorganic Chemistry, 1984)
- Oxygenase model reactions. 1. Intra- and extradiol oxygenations of 3,5-di-tert-butylcatechol catalyzed by (bipyridine)(pyridine)iron(III) complex (Journal of the American Chemical Society, 1986)
- Catalytic oxidation of 3,5-Di-tert-butylcatechol by a series of mononuclear manganese complexes: synthesis, structure, and kinetic investigation. (Inorganic Chemistry, 2003)
- Catechol oxidations. Characterization of metal complexes of 3,5-di-tert-butyl-1,2-quinone 1-(2-hydroxy-3,5-di-tert-butylphenyl)imine formed by the aerial oxidation of 3,5-di-tert-butylcatechol in the presence of ammonia and divalent metal ions (Inorganic Chemistry, 1975)
- Chemistry of superoxide ion. I. Oxidation of 3,5-di-tert-butylcatechol with KO2. (Journal of the American Chemical Society, 1976)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 3,5-di-t-butyl catechol
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SMILESCC(C)(C)C1=CC(=C(C(=C1)O)O)C(C)(C)C
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InChIKeyPJZLSMMERMMQBJ-UHFFFAOYSA-N
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