| Weight | 180.25 g/mol |
|---|---|
| Formula | C14H12 |
| Hydrogen Acceptors | 0 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 2 |
1,1-DIPHENYLETHYLENE (530-48-3)
Score:
#2279 in Physics
,
#7040 in Chemistry
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- Precise syntheses of chain-multi-functionalized polymers, star-branched polymers, star-linear block polymers, densely branched polymers, and dendritic branched polymers based on iterative approach using functionalized 1,1-diphenylethylene derivatives (Progress in Polymer Science, 2005)
- Radical ions in photochemistry. I. 1,1-Diphenylethylene cation radical (Journal of the American Chemical Society, 1973)
- Redox-photosensitized reactions. 7. Aromatic hydrocarbon-photosensitized electron-transfer reactions of furan, methylated furans, 1,1-diphenylethylene, and indene with p-dicyanobenzene (Journal of the American Chemical Society, 1981)
- Applications of 1,1-Diphenylethylene Chemistry in Anionic Synthesis of Polymers with Controlled Structures (Advances in Polymer Science, 2000)
- Dibenzofulvene, a 1,1-Diphenylethylene Analogue, Gives a -Stacked Polymer by Anionic, Free-Radical, and Cationic Catalysts (Journal of the American Chemical Society, 2001)
- Living Anionic Surface-Initiated Polymerization (LASIP) of Styrene from Clay Nanoparticles Using Surface Bound 1,1-Diphenylethylene (DPE) Initiators (Langmuir, 2002)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC=C(C1=CC=CC=C1)C2=CC=CC=C2
-
InChIKeyZMYIIHDQURVDRB-UHFFFAOYSA-N
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Synthesis
Reactant
+
1-Hydroxy-1,2-benziodoxol-3(1H)-one 1-oxide
(Nicolaou IBX dehydrogenation)
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1,1-DIPHENYLETHYLENE
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