2303-17-5
2303-17-5
Chemical Structure
Triallate
- CAS No.: 2303-17-5
- Formula:C10H16Cl3NOS
- Molecular Weight:304.66
IUPAC Name: S-(2,3,3-trichloroallyl) diisopropylcarbamothioate
InChIKey: MWBPRDONLNQCFV-UHFFFAOYSA-N
SMILES: O=C(SC/C(Cl)=C(Cl)/Cl)N(C(C)C)C(C)C
Biological Activity: Triallate is a selective thiocarbamate herbicide. Triallate regulates the biosynthesis of very-long-chain fatty acids and inhibits the elongation and division of plant cells. Triallate is used to control wild oats in barley, spring wheat, durum wheat, winter wheat and sugar beets[1][2][3][4][5][6][7].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Triallate | 99.02% | Triallate is a selective thiocarbamate herbicide. Triallate regulates the biosynthesis of very-long-chain fatty acids and inhibits the elongation and division of plant cells. Triallate is used to control wild oats in barley, spring wheat, durum wheat, winter wheat and sugar beets. | ||||||||||||||||||||
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Triallate (Standard) | ≥98% | Triallate (Standard) is the analytical standard of Triallate (HY-119435). This product is intended for research and analytical applications. Triallate is a selective thiocarbamate herbicide. Triallate regulates the biosynthesis of very-long-chain fatty acids and inhibits the elongation and division of plant cells. Triallate is used to control wild oats in barley, spring wheat, durum wheat, winter wheat and sugar beets | ||||||||||||||||||||
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Structural Analogs
-
Similarity Score 0.56
HY-W009690N,N,N',N'-Tetraacetylethylenediamine -
Similarity Score 0.54
HY-B0240Disulfiram -
Similarity Score 0.54
HY-B2149Quadrol -
Similarity Score 0.53
HY-17455RPramiracetam (Standard) -
Similarity Score 0.53
HY-W1278103,3',3''-Nitrilotripropionic Acid -
Similarity Score 0.52
HY-129912ARN1,N8-Diacetylspermidine hydrochloride (Standard) -
Similarity Score 0.52
HY-129912N1,N8-Diacetylspermidine -
Similarity Score 0.52
HY-165255N-Isobutyl decanamide -
Similarity Score 0.52
HY-W007801Tetrapropylammonium perruthenate -
Explore the MedChemAI to find more analogs
References
- [1]. Lapadula DM, et al. Absence of delayed neurotoxicity and increased plasma butyrylcholinesterase activity in triallate-treated hens. Fundam Appl Toxicol. 1990;14(1):191-198. [Content Brief]
- [2]. Alehashem M, et al. Linking pesticide exposure to neurodegenerative diseases: An in vitro investigation with human neuroblastoma cells. Sci Total Environ. 2024 Jul 10;933:173041. [Content Brief]
- [3]. Alehashem M, et al. Linking pesticide exposure to neurodegenerative diseases: An in vitro investigation with human neuroblastoma cells. Sci Total Environ. 2024;933:173041. [Content Brief]
- [4]. Quistad GB, et al. Aldehyde dehydrogenase of mice inhibited by thiocarbamate herbicides. Life Sci. 1994;55(20):1537-1544. [Content Brief]
- [5]. Ingolf Schuphan, et al. S-Chloroallyl thiocarbamate herbicides: chemical and biological formation and rearrangement of diallate and triallate sulfoxides. J. Agric. Food Chem. 1979, 27, 5, 1060-1067.
- [6]. K.A. Fayez, et al. The influence of herbicides on the growth and proline content of primary roots and on the ultrastructure of root caps. Environmental and Ex~invmtal Botany, Vol. 36, No. 1, pp. 71 81, 1996.
- [7]. J. D. Banting, et al. Effect of Diallate and Triallate on Wild Oat and Wheat Cells. Weed Science, Volume 18 , Issue 1 , January 1970 , pp. 80-84.
