Tebufloquin
| Structural formula | |||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|||||||||||||
| General | |||||||||||||
| Surname | Tebufloquin | ||||||||||||
| other names |
6- (1,1-Dimethylethyl) -8-fluoro-2,3-dimethyl-4-quinolinylacetate |
||||||||||||
| Molecular formula | C 17 H 20 FNO 2 | ||||||||||||
| External identifiers / databases | |||||||||||||
|
|||||||||||||
| properties | |||||||||||||
| Molar mass | 289.34 g mol −1 | ||||||||||||
| Physical state |
firmly |
||||||||||||
| density |
1.12 g cm −3 (bulk density) |
||||||||||||
| Melting point |
379.6 ° C |
||||||||||||
| safety instructions | |||||||||||||
|
|||||||||||||
| As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions . | |||||||||||||
Tebufloquin is a chemical compound from the quinoline group .
Extraction and presentation
Tebufloquin can be obtained by O -acylation of 6- tert- butyl-8-fluoro-2,3-dimethylquinolin-4 (1 H ) -one with a mixture of acetic anhydride and pyridine .
use
Tebufloquin is used as a fungicide to control Magnaporthe grisea in rice. It was discovered by Meiji Seika Kaisha in 2000.
Individual evidence
- ↑ a b Entry on tebufloquine in the Pesticide Properties DataBase (PPDB) of the University of Hertfordshire , accessed on December 27, 2014.
- ↑ This substance has either not yet been classified with regard to its hazardousness or a reliable and citable source has not yet been found.
- ^ A b Ulrich Schirmer, Peter Jeschke, Matthias Witschel: Modern Crop Protection Compounds: Herbicides . John Wiley & Sons, 2012, ISBN 978-3-527-32965-6 , pp. 879 ( limited preview in Google Book search).