1258836-72-4
Chemical Structure
Trifludimoxazin
- CAS No.: 1258836-72-4
- Formula:C16H11F3N4O4S
- Molecular Weight:412.34
IUPAC Name: 1,5-dimethyl-6-thioxo-3-(2,2,7-trifluoro-3-oxo-4-(prop-2-yn-1-yl)-3,4-dihydro-2H-benzo[b][1,4]oxazin-6-yl)-1,3,5-triazinane-2,4-dione
InChIKey: AZHZOGYUMMIAOF-UHFFFAOYSA-N
SMILES: O=C(N(C1=C(F)C=C(OC(F)(F)C(N2CC#C)=O)C2=C1)C(N3C)=O)N(C)C3=S
Biological Activity: Trifludimoxazin is a click chemistry reagent, a protoporphyrinogen oxidase (PPO) inhibitor and herbicide. Trifludimoxazin inhibits PPO, accumulates reactive oxygen species, damages cell membranes, and thereby causes weed death. Trifludimoxazin exhibits high-efficiency activity in controlling broadleaf weeds and grassy weeds[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Trifludimoxazin | 98.05% | Trifludimoxazin is a click chemistry reagent, a protoporphyrinogen oxidase (PPO) inhibitor and herbicide. Trifludimoxazin inhibits PPO, accumulates reactive oxygen species, damages cell membranes, and thereby causes weed death. Trifludimoxazin exhibits high-efficiency activity in controlling broadleaf weeds and grassy weeds. | ||||||||||||||||||||
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References
- [1]. Porri A, et al. Inhibition profile of trifludimoxazin towards PPO2 target site mutations. Pest Manag Sci. 2023;79(2):507-519. [Content Brief]
- [2]. Liliana Parra Rapado, et al. Complementary activity of Trifludimoxazin and Saflufenacil when used in combination for postemergence and residual weed control. Weed Sci. 73(e14), 1–11.
