Cas no 135990-29-3 (Triflusulfuron)
Triflusulfuron Chemical and Physical Properties
Names and Identifiers
-
- Triflusulfuron
- 2-[[4-(Dimethylamino)-6-(2,2,2-trifluoroethoxy)-1,3,5-triazin-2-yl]carbamoylsulfamoyl]-3-methylbenzoic acid
- 2-[[[[[4-(dimethylamino)-6-(2,2,2-trifluoroethoxy)-1,3,5-triazin-2-yl]amino]carbonyl]amino]sulfonyl]-3-methylbenzoic acid
- 2-[[4-(dimethylamino)-6-(2,2,2-trifluoroethoxy)-1,3,5-triazin-2-yl]carbamoylsulfamo
- 2-[4-dimethylamino-6-(2,2,2-trifluoroethoxy)-1,3,5-triazin-2-ylcarbamoylsulfamoyl]-m-toluic acid
- Benzoic acid,2-(((((4-(dimethylamino)-6-(2,2,2-trifluoroethoxy)-1,3,5-triazin-2-yl)amino)carbonyl)amino)sulfonyl)-3-methyl
- Triflusulfuron [ISO]
- 2-(((((4-(DIMETHYLAMINO)-6-(2,2,2-TRIFLUOROETHOXY)-1,3,5-TRIAZIN-2-YL)AMINO)CARBONYL)AMINO)SULFONYL)-3-METHYLBENZOIC ACID
- SCHEMBL55458
- NS00001864
- CHEBI:142847
- 2-(4-DIMETHYLAMINO-6-(2,2,2-TRIFLUOROETHOXY)-1,3,5-TRIAZIN-2-YLCARBAMOYLSULFAMOYL)-M-TOLUIC ACID
- DTXSID10159614
- Benzoic acid, 2-(((((4-(dimethylamino)-6-(2,2,2-trifluoroethoxy)-1,3,5-triazin-2-yl)amino)carbonyl)amino)sulfonyl)-3-methyl-
- triflusulfuron-methyl TP5
- 019NSK845Q
- 2-({[4-(dimethylamino)-6-(2,2,2-trifluoroethoxy)-1,3,5-triazin-2-yl]carbamoyl}sulfamoyl)-3-methylbenzoic acid
- UNII-019NSK845Q
- AKTQJCBOGPBERP-UHFFFAOYSA-N
- 2-(N-{[4-(dimethylamino)-6-(2,2,2-trifluoroethoxy)-1,3,5-triazin-2-yl]carbamoyl}sulfamoyl)-3-methylbenzoic acid
- Q27231418
- 135990-29-3
-
- Inchi： 1S/C16H17F3N6O6S/c1-8-5-4-6-9(11(26)27)10(8)32(29,30)24-14(28)21-12-20-13(25(2)3)23-15(22-12)31-7-16(17,18)19/h4-6H,7H2,1-3H3,(H,26,27)(H2,20,21,22,23,24,28)
- InChI Key： AKTQJCBOGPBERP-UHFFFAOYSA-N
- SMILES： S(C1C(C(=O)O)=CC=CC=1C)(NC(NC1N=C(N=C(N=1)N(C)C)OCC(F)(F)F)=O)(=O)=O
Computed Properties
- Exact Mass: 478.08800
- Monoisotopic Mass: 478.088
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 3
- Hydrogen Bond Acceptor Count: 13
- Heavy Atom Count: 32
- Rotatable Bond Count: 7
- Complexity: 777
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- Topological Polar Surface Area: 172A^2
- XLogP3: 2.8
Experimental Properties
- Density: 1.571
- Melting Point: 160-163oC
- Boiling Point: °Cat760mmHg
- Flash Point: °C
- Refractive Index: 1.578
- PSA: 172.09000
- LogP: 2.94040
Triflusulfuron Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| TRC | T782005-10mg |
Triflusulfuron |
135990-29-3 | 10mg |
$ 540.00 | 2023-09-05 | ||
| TRC | T782005-25mg |
Triflusulfuron |
135990-29-3 | 25mg |
$ 1047.00 | 2023-09-05 | ||
| TRC | T782005-100mg |
Triflusulfuron |
135990-29-3 | 100mg |
$ 3985.00 | 2023-09-05 | ||
| A2B Chem LLC | AE45223-100mg |
Triflusulfuron |
135990-29-3 | 100mg |
$1215.00 | 2024-04-20 |
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Triflusulfuron Related Literature
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Sergio C. Nanita,Laura G. Kaldon,David L. Bailey Anal. Methods 2015 7 2300
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Sergio C. Nanita Analyst 2011 136 285
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Christina K. Remucal Environ. Sci.: Processes Impacts 2014 16 628
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Mike May Pestic. Outlook 2001 12 188
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Abera Gure,Negussie Megersa,Negussie Retta Anal. Methods 2014 6 4633
Additional information on Triflusulfuron
Triflusulfuron: A Comprehensive Overview
Triflusulfuron, also known by its CAS number 135990-29-3, is a highly effective herbicide that has gained significant attention in the agricultural and environmental sectors. This compound belongs to the sulfonylurea class of herbicides, which are widely used for their ability to control a broad spectrum of weeds. Triflusulfuron is particularly noted for its low application rate and high efficiency, making it a preferred choice for farmers and agricultural professionals worldwide.
The chemical structure of Triflusulfuron is characterized by a sulfonylurea group, which plays a crucial role in its herbicidal activity. This group is responsible for inhibiting the enzyme acetolactate synthase (ALS), which is essential for the biosynthesis of branched-chain amino acids in plants. By targeting this enzyme, Triflusulfuron effectively disrupts the growth and development of weeds, leading to their eventual death. Recent studies have highlighted the specificity of Triflusulfuron's action, which minimizes its impact on non-target crops and enhances its selectivity as a herbicide.
One of the most notable advancements in the application of Triflusulfuron is its use in integrated pest management (IPM) systems. Farmers are increasingly adopting IPM strategies to reduce reliance on chemical inputs and promote sustainable agriculture. Triflusulfuron's compatibility with these systems has been validated by recent research, which demonstrates its ability to work synergistically with other pest control methods. For instance, studies have shown that combining Triflusulfuron with biological control agents can significantly reduce weed populations while maintaining crop health and productivity.
The environmental impact of Triflusulfuron has also been a focal point of recent investigations. Research indicates that Triflusulfuron degrades relatively quickly in soil, reducing the risk of long-term environmental contamination. However, its persistence in water bodies remains a concern, particularly in regions with high rainfall or irrigation practices. To address this issue, scientists have developed modified formulations of Triflusulfuron that enhance its stability under specific environmental conditions while minimizing leaching into water systems.
In terms of application methods, Triflusulfuron can be applied as a pre-emergent or post-emergent herbicide, depending on the specific weed species and crop rotation practices. Its versatility makes it suitable for use in various cropping systems, including cereals, oilseeds, and vegetables. Recent trials have demonstrated the effectiveness of Triflusulfuron in controlling glyphosate-resistant weeds, a growing challenge in modern agriculture. This capability underscores its importance as a tool for managing herbicide resistance and ensuring sustainable crop production.
The global market for Triflusulfuron has seen steady growth over the past decade, driven by increasing demand from developing countries with expanding agricultural sectors. According to market analysis reports, the herbicide's demand is expected to rise further due to its cost-effectiveness and compatibility with organic farming practices. However, regulatory scrutiny regarding the safety and efficacy of sulfonylurea herbicides continues to influence market dynamics. Researchers are actively exploring ways to optimize Triflusulfuron's formulation to meet stringent safety standards while maintaining its performance attributes.
In conclusion, Triflusulfuron (CAS No. 135990-29-3) stands out as a critical component in modern weed management strategies. Its unique mode of action, coupled with advancements in formulation technology and application techniques, positions it as a valuable tool for achieving sustainable agricultural outcomes. As research continues to uncover new insights into its environmental behavior and efficacy against resistant weeds, Triflusulfuron is poised to remain a cornerstone of agricultural pest management for years to come.
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