| Weight | 200.262 g/mol |
|---|---|
| Formula | C12H8OS |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 0 |
Phenoxathiin (262-20-4)
Score:
#1698 in Physics
,
#5281 in Chemistry
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- 2,8-Dimethyl-4-(carboxymethyl)-6-(aminomethyl)phenoxathiin S-dioxide: an organic substitute for the .beta.-turn in peptides? (Journal of the American Chemical Society, 1986)
- High-Efficiency Blue Organic Light-Emitting Diodes Based on Thermally Activated Delayed Fluorescence from Phenoxaphosphine and Phenoxathiin Derivatives. (Advanced Materials, 2016)
- The Oxidation of Dibenzothiophene and Phenoxathiin with Hydrogen Peroxide (Journal of the American Chemical Society, 1952)
- A modular approach to polymer architecture control via catenation of prefabricated biomolecular segments : Polymers containing parallel -sheets templated by a phenoxathiin-based reverse turn mimic (Macromolecules, 1997)
- Spectral study and molecular modeling of the inclusion complexes of -cyclodextrin with some phenoxathiin derivatives (Journal of Physical Chemistry B, 2002)
- Hydroprocessing of dibenzothiophene, phenothiazine, phenoxathiin, thianthrene, and thioxanthene on a sulfided NiOMoO3-Al2O3 catalyst (Journal of Catalysis, 1986)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC=C2C(=C1)OC3=CC=CC=C3S2
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InChIKeyGJSGGHOYGKMUPT-UHFFFAOYSA-N
- Pubchem - Phenoxathiin
- Wikipedia - phenoxathiin
Phenoxathiin (dibenzooxathiane) C12H8OS is a heterocyclic compound of molecular weight 200.25632 g/mol with the CAS Registry Number 262-20-4. Diphenyl ether is a starting material in the production of phenoxathiin via the Ferrario reaction. Phenoxathiin is used in polyamide and polyimide production.
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Phenoxathiin
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