96525-23-4
Chemical Structure
Flurtamone
- CAS. Nr.: 96525-23-4
- Formula:C18H14F3NO2
- Molecular Weight:333.30
IUPAC Name: 5-(methylamino)-2-phenyl-4-(3-(trifluoromethyl)phenyl)furan-3(2H)-one
InChIKey: NYRMIJKDBAQCHC-UHFFFAOYSA-N
SMILES: O=C1C(OC(NC)=C1C2=CC=CC(C(F)(F)F)=C2)C3=CC=CC=C3
Biological Activity: Flurtamone is a herbicide that interferes with carotenoid biosynthesis by inhibiting phytoene desaturase, blocking the conversion of phytoene to ζ-carotene. Flurtamone can cause the accumulation of phytoene, leading to photooxidative destruction of chlorophyll and plant albinism. Flurtamone comprises a pair of chiral enantiomers, R-flurtamone and S-flurtamone, with R-flurtamone exhibiting significantly stronger herbicidal activity against target weeds. Flurtamone is toxic to Selenastrum capricornutum. Flurtamone can control broadleaf weeds and grass weeds as well as various weeds, and can be used in herbicide-related research[1][2][3].
| Art. -Nr. | Produktname | Reinheit | Beschreibung | Pricing | |||||||||||||||||||
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Flurtamone | 99.95% | Flurtamone is a herbicide that interferes with carotenoid biosynthesis by inhibiting phytoene desaturase, blocking the conversion of phytoene to ζ-carotene. Flurtamone can cause the accumulation of phytoene, leading to photooxidative destruction of chlorophyll and plant albinism. Flurtamone comprises a pair of chiral enantiomers, R-flurtamone and S-flurtamone, with R-flurtamone exhibiting significantly stronger herbicidal activity against target weeds. Flurtamone is toxic to Selenastrum capricornutum. Flurtamone can control broadleaf weeds and grass weeds as well as various weeds, and can be used in herbicide-related research. | ||||||||||||||||||||
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Flurtamone (Standard) | ≥98% | Flurtamone (Standard) is the analytical standard of Flurtamone. This product is intended for research and analytical applications. Flurtamone is a chiral herbicide with acute toxicity levels to Selenastrum capricornutum. | ||||||||||||||||||||
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References
- [1]. Sandmann G, et al. Bleaching herbicide flurtamone interferes with phytoene desaturase. Plant physiology. 1990 Oct;94(2):476-8.
- [2]. Zhang Y, et al. Comprehensive Assessment of Enantioselective Bioactivity, Toxicity, and Dissipation in Soil of the Chiral Herbicide Flurtamone. Journal of agricultural and food chemistry. 2023 Mar 29;71(12):4810-4816. [Content Brief]
- [3]. Kim J S, et al. Death mechanisms caused by carotenoid biosynthesis inhibitors in green and in undeveloped plant tissues. Pesticide Biochemistry and Physiology. 2004;78(3):127-139.
