Weight | 220.312 g/mol |
---|---|
Formula | C14H20O2 |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 0 |
Aromatic Rings | 0 |
Rotatable Bonds | 0 |
3383-21-9 (3383-21-9)
3,5-DTBBQ · 3,5-di-tert-butyl-1,2-benzoquinone · 3,5-di-t-butyl-o-benzoquinone
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- Characterization of Redox States of Ru(OH2)(Q)(tpy)2+ (Q = 3,5-di-tert-butyl-1,2-benzoquinone, tpy = 2,2#:6#,2#-terpyridine)and Related Species through Experimental and Theoretical Studies (Inorganic Chemistry, 2009)
- Mechanism of the Electrochemical Reduction of 3,5-Di-tert-butyl-1,2-benzoquinone. Evidence for a Concerted Electron and Proton Transfer Reaction Involving a Hydrogen-Bonded Complex as Reactant (Journal of Physical Chemistry B, 2001)
- Metal(II) derivatives of 3,5-di-tert-butyl-1,2-o-benzoquinone. EPR study of conformation in biradicals (Journal of the American Chemical Society, 1991)
- Redox reactions of 3,5-di-tert-butyl-1,2-benzoquinone. Implications for reversal of paper yellowing (Canadian Journal of Chemistry, 1995)
- Oxidative substitution of pentacarbonylmanganese(1-) by 3,5-di-tert-butyl-1,2-benzoquinone. Synthesis and characterization of the unsaturated Mn(CO)3(DBCat)- anion (Inorganic Chemistry, 1990)
- Coordination compounds of indium. XLVI: Indium(I) derivatives of 3,5-di-tert-butyl-1,2-o-benzoquinone (Inorganic Chemistry, 1989)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 3,5-DTBBQ
- 3,5-di-tert-butyl-1,2-benzoquinone
- 3,5-di-t-butyl-o-benzoquinone
-
SMILESCC(C)(C)C1=CC(=O)C(=O)C(=C1)C(C)(C)C
-
InChIKeyNOUZOVBGCDDMSX-UHFFFAOYSA-N
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Synthesis
Reactant
+
dimethyl sulfide
(Corey-Kim oxidation of secondary alcohols)
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