Methyl 2-[[[4-chloro-2-fluoro-5-[(2,2,2-trifluoroethyl)thio]phenyl]amino]methyl]benzoate
![Methyl 2-[[[4-chloro-2-fluoro-5-[(2,2,2-trifluoroethyl)thio]phenyl]amino]methyl]benzoate Structure](CAS/20210305/GIF/2566451-67-8.gif)
- CAS No.
- 2566451-67-8
- Chemical Name:
- Methyl 2-[[[4-chloro-2-fluoro-5-[(2,2,2-trifluoroethyl)thio]phenyl]amino]methyl]benzoate
- Synonyms
- Methyl 2-[[[4-chloro-2-fluoro-5-[(2,2,2-trifluoroethyl)thio]phenyl]amino]methyl]benzoate;methyl 2-[({4-chloro-2-fluoro-5-[(2,2,2-trifluoroethyl)sulfanyl]phenyl}amino)methyl]benzoate
- CBNumber:
- CB213499314
- Molecular Formula:
- C17H14ClF4NO2S
- Molecular Weight:
- 407.81
- MDL Number:
- MOL File:
- 2566451-67-8.mol
Methyl 2-[[[4-chloro-2-fluoro-5-[(2,2,2-trifluoroethyl)thio]phenyl]amino]methyl]benzoate price
| Manufacturer | Product number | Product description | CAS number | Packaging | Price | Updated | Buy |
|---|---|---|---|---|---|---|---|
| aablocks | AA02AIND | methyl 2-[({4-chloro-2-fluoro-5-[(2,2,2-trifluoroethyl)sulfanyl]phenyl}amino)methyl]benzoate 95.00% | 2566451-67-8 | 50mg | $323 | 2026-06-02 | Buy |
| aablocks | AA02AIND | methyl 2-[({4-chloro-2-fluoro-5-[(2,2,2-trifluoroethyl)sulfanyl]phenyl}amino)methyl]benzoate 95.00% | 2566451-67-8 | 100mg | $462 | 2026-06-02 | Buy |
| aablocks | AA02AIND | methyl 2-[({4-chloro-2-fluoro-5-[(2,2,2-trifluoroethyl)sulfanyl]phenyl}amino)methyl]benzoate 95.00% | 2566451-67-8 | 250mg | $642 | 2026-06-02 | Buy |
| aablocks | AA02AIND | methyl 2-[({4-chloro-2-fluoro-5-[(2,2,2-trifluoroethyl)sulfanyl]phenyl}amino)methyl]benzoate 95.00% | 2566451-67-8 | 500mg | $988 | 2026-06-02 | Buy |
| aablocks | AA02AIND | methyl 2-[({4-chloro-2-fluoro-5-[(2,2,2-trifluoroethyl)sulfanyl]phenyl}amino)methyl]benzoate 95.00% | 2566451-67-8 | 1g | $1254 | 2026-06-02 | Buy |
Methyl 2-[[[4-chloro-2-fluoro-5-[(2,2,2-trifluoroethyl)thio]phenyl]amino]methyl]benzoate Chemical Properties, Uses, Production
Production Methods
Bentioflumin is produced through a multi-step synthesis that constructs its benzamide-based acaricide framework. The process begins with the preparation of a substituted aniline derivative containing chloro, fluoro, and trifluoroethylthio substituents on the aromatic ring. This intermediate is then coupled via nucleophilic substitution with a benzylamine fragment to introduce the aminomethyl linkage. Finally, esterification with methanol yields the methyl benzoate moiety, completing the structure. Careful control of reaction conditions ensures the correct substitution pattern and stability of the trifluoroethylthio group, after which the product is purified and formulated for agricultural use.
Mechanism of action
Acts as a mitochondrial electron transport inhibitor, specifically targeting complex II (succinate dehydrogenase) in mites. By disrupting energy production in the mitochondria, it causes rapid paralysis and death of target species.
Pesticide Type
Acaricide; Insecticide
Methyl 2-[[[4-chloro-2-fluoro-5-[(2,2,2-trifluoroethyl)thio]phenyl]amino]methyl]benzoate Preparation Products And Raw materials
Raw materials
Preparation Products
Methyl 2-[[[4-chloro-2-fluoro-5-[(2,2,2-trifluoroethyl)thio]phenyl]amino]methyl]benzoate Suppliers
| Supplier | Tel | Country | ProdList | Advantage | |
|---|---|---|---|---|---|
| Hangzhou Oder Technology Co., Ltd. | 0571-88772972-0 15057128248 | 2746615063@qq.com | China | 2669 | 58 |
| Supplier | Advantage |
|---|---|
| Hangzhou Oder Technology Co., Ltd. | 58 |
