Benzenetellurol
| Benzenetellurol molecule | |
| File:Benzenetellurol-3D-vdW.png | |
| Names | |
|---|---|
| IUPAC name
Benzenetellurol[2]
| |
| Other names
Tellurophenol[1]
| |
| Identifiers | |
3D model (JSmol)
|
|
| ChemSpider | |
| ECHA InfoCard | Lua error in Module:Wikidata at line 879: attempt to index field 'wikibase' (a nil value). Lua error in Module:Wikidata at line 879: attempt to index field 'wikibase' (a nil value). |
| E number | Lua error in Module:Wikidata at line 879: attempt to index field 'wikibase' (a nil value). |
CompTox Dashboard (EPA)
|
|
| |
| |
| Properties | |
| C 6H 5TeH | |
| Molar mass | 205.71 g·mol−1 |
| Appearance | Colorless oily liquid |
| Odor | Unpleasant |
| Solubility | Soluble in organic solvents |
| Related compounds | |
Related compounds
|
|
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| Infobox references | |
Benzenetellurol is an organotellurium compound with the chemical formula C
6H
5TeH, often abbreviated as PhTeH, where Ph stands for phenyl. It is an analog of phenol C
6H
5OH, where oxygen is replaced by tellurium.
Benzenetellurol can be synthesized by methanolysis of phenyl trimethylsilyl telluride (C
6H
5TeSi(CH
3)
3) or reduction of diphenyl ditelluride with phosphinic acid or sodium borohydride. It is unstable. It is used as a reducing agent in situ in organic synthesis, for example, to reduce aromatic nitro compounds to amines.[3][4]
References
- ↑ https://www.chemspider.com/Chemical-Structure.4414346.html
- ↑ https://pubchem.ncbi.nlm.nih.gov/compound/Benzenetellurol
- ↑ https://academic.oup.com/chemlett/article-abstract/13/6/853/7415054?redirectedFrom=fulltext&login=false
- ↑ https://books.google.com.br/books?id=0GNno3CX0PcC&pg=PA5715&f=false#v=onepage&q&f=false
This article "Benzenetellurol" is from Wikipedia. The list of its authors can be seen in its historical and/or the page Edithistory:Benzenetellurol. Articles copied from Draft Namespace on Wikipedia could be seen on the Draft Namespace of Wikipedia and not main one.
