492-22-8
Chemical Structure
Thioxanthone
- CAS No.: 492-22-8
- Formula:C13H8OS
- Molecular Weight:212.27
IUPAC Name: 9H-thioxanthen-9-one
InChIKey: YRHRIQCWCFGUEQ-UHFFFAOYSA-N
SMILES: O=C1C2=C(SC3=C1C=CC=C3)C=CC=C2
Biological Activity: Thioxanthone is a powerful photocatalyst for organic reactions. Thioxanthone mediates energy transfer, single-electron transfer, and hydrogen atom transfer processes. As a photoredox catalyst, Thioxanthone is used in nickel-catalyzed self-coupling reactions of aryl halides, arylation reactions of H-phosphine oxides/H-phosphites, decarbonylation reactions of cyclopropenones, and reactions generating acyl radicals from aromatic aldehydes[1].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
Thioxanthone | 98.31% | Thioxanthone is a powerful photocatalyst for organic reactions. Thioxanthone mediates energy transfer, single-electron transfer, and hydrogen atom transfer processes. As a photoredox catalyst, Thioxanthone is used in nickel-catalyzed self-coupling reactions of aryl halides, arylation reactions of H-phosphine oxides/H-phosphites, decarbonylation reactions of cyclopropenones, and reactions generating acyl radicals from aromatic aldehydes. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
Keywords
