| Weight | 212.273 g/mol |
|---|---|
| Formula | C13H8OS |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 3 |
| Rotatable Bonds | 0 |
Thioxanthen-9-one (492-22-8)
thioxanthone
Score:
#2364 in Physics
,
#7226 in Chemistry
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- Novel Thermally Activated Delayed Fluorescence MaterialsThioxanthone Derivatives and Their Applications for Highly Efficient OLEDs (Advanced Materials, 2014)
- Thioxanthone-Anthracene: A New Photoinitiator for Free Radical Polymerization in the Presence of Oxygen (Macromolecules, 2007)
- Synthesis and Characterization of Polymeric Thioxanthone Photoinitatiors via Double Click Reactions (Macromolecules, 2008)
- Mechanistic Study of Photoinitiated Free Radical Polymerization Using Thioxanthone Thioacetic Acid as One-Component Type II Photoinitiator (Macromolecules, 2005)
- On the photoinitiation of free radical polymerization-laser flash photolysis investigations on thioxanthone derivatives (Macromolecular Chemistry and Physics, 1981)
- Thioxanthone-Fluorenes as Visible Light Photoinitiators for Free Radical Polymerization (Macromolecules, 2010)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - thioxanthone
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SMILESC1=CC=C2C(=C1)C(=O)C3=CC=CC=C3S2
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InChIKeyYRHRIQCWCFGUEQ-UHFFFAOYSA-N
- Pubchem - Thioxanthen-9-one
- Wikipedia - thioxanthone
Thioxanthone is a heterocyclic compound that is a sulfur analog of xanthone. Thioxanthone can be prepared by the reaction of diphenyl sulfide with phosgene in the presence of catalytic aluminium chloride. This synthesis can be seen as a special case of the Friedel-Crafts acylation.
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Thioxanthen-9-one
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