| Weight | 238.374 g/mol |
|---|---|
| Formula | C18H22 |
| Hydrogen Acceptors | 0 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 3 |
2,3-Dimethyl-2,3-diphenylbutane (1889-67-4)
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- Photochemistry of 2,3-dimethyl-2,3-diphenylbutane: carbon-carbon homolysis and protonation-induced side-chain fragmentation (The Journal of Physical Chemistry, 1992)
- 2,3-Dimethyl-2,3-diphenylbutane mediated grafting of vinyltriethoxysilane to polyethylene: a novel radical initiation system (Polymer, 2003)
- Mechanism and selectivity of 2,3-dimethyl-2,3-diphenylbutane mediated addition of vinyltriethoxysilane to polyethylene (European Polymer Journal, 2006)
- An infrared and Raman spectroscopic study of rotational isomerism in 2,3-dimethyl-2,3-diphenylbutane, the fluoro-, chloro-, and bromo-substituted 2,3-dimethyl-2,3-di-p-halogenophenylbutanes and 1,2-diphenyltetrachloroethane (Journal of The Chemical Society B: Physical Organic, 1970)
- ChemInform Abstract: Photochemistry of 2,3Dimethyl2,3diphenylbutane: CC Homolysis and ProtonationInduced SideChain Fragmentation. (ChemInform, 2010)
- ChemInform Abstract: Lewis-Acid Mediated Formation of (.+-.)-(cis)-2,6-Dimethyl-4,4- diphenyl-1,3-dioxane from (.+-.)-1,1-Diphenylbutane-1,3-diol. (ChemInform, 2010)
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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)(C1=CC=CC=C1)C(C)(C)C2=CC=CC=C2
-
InChIKeyHGTUJZTUQFXBIH-UHFFFAOYSA-N
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Synthesis
benzene
+
Reactant
(Friedel-Crafts alkylation)
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