| Weight | 228.254 g/mol |
|---|---|
| Formula | C16H8N2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 3 |
| Rotatable Bonds | 0 |
9,10-Dicyanoanthracene (1217-45-4)
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- Electron Transfer and Singlet Oxygen Mechanisms in the Photooxygenation of Dibutyl Sulfide and Thioanisole in MeCN Sensitized by N-Methylquinolinium Tetrafluoborate and 9,10-Dicyanoanthracene. The Probable Involvement of a Thiadioxirane Intermediate in Electron Transfer Photooxygenations (Journal of the American Chemical Society, 2003)
- Mechanisms of photooxygenation. 2. Formation of 1,2-dioxetanes via 9,10-dicyanoanthracene-sensitized electron-transfer processes [14] (Journal of the American Chemical Society, 1980)
- Formation of an ozonide by electron-transfer photooxygenation of tetraphenyloxirane. Cosensitization by 9,10-dicyanoanthracene and biphenyl (Journal of the American Chemical Society, 1983)
- Chemistry of singlet oxygen. 39. 9,10-Dicyanoanthracene-sensitized formation of singlet oxygen (The Journal of Physical Chemistry, 1983)
- Photoadditions of ethers, thioethers, and amines to 9,10-dicyanoanthracene by electron transfer pathways (Journal of Organic Chemistry, 1988)
- PHOTOINDUCED ELECTRON TRANSFER REACTIONS OF BENZYL PHENYL SULFIDES PROMOTED BY 9,10-DICYANOANTHRACENE (Tetrahedron, 1997)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC=C2C(=C1)C(=C3C=CC=CC3=C2C#N)C#N
-
InChIKeyBIOPPFDHKHWJIA-UHFFFAOYSA-N
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