Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C15H9ClF3N2O6S.Na |
| Molecular Weight | 460.745 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
[Na+].CS(=O)(=O)[N-]C(=O)C1=CC(OC2=CC=C(C=C2Cl)C(F)(F)F)=CC=C1[N+]([O-])=O
InChI
InChIKey=CRHGSCXKJPJNAB-UHFFFAOYSA-M
InChI=1S/C15H10ClF3N2O6S.Na/c1-28(25,26)20-14(22)10-7-9(3-4-12(10)21(23)24)27-13-5-2-8(6-11(13)16)15(17,18)19;/h2-7H,1H3,(H,20,22);/q;+1/p-1
| Molecular Formula | C15H10ClF3N2O6S |
| Molecular Weight | 438.763 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
| Molecular Formula | Na |
| Molecular Weight | 22.98976928 |
| Charge | 1 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Assessment of possible carcinogenicity of oxyfluorfen to humans using mode of action analysis of rodent liver effects. | 2012-08 |
|
| [Isolation, identification and soil remediation of atrazine-degrading strain T3 AB1]. | 2010-12 |
|
| [Determination of biphenyl ether herbicides in water using HPLC with cloud-point extraction]. | 2010-01 |
|
| Biodegradation of fomesafen by strain Lysinibacillus sp. ZB-1 isolated from soil. | 2009-12 |
|
| Effects of diquat and fomesafen applied alone and in combination with a nonylphenol polyethoxylate adjuvant on Lemna minor in aquatic indoor microcosms. | 2009-03 |
|
| Effect of a toxicant on phagocytosis pathways in the freshwater snail Lymnaea stagnalis. | 2008-07 |
|
| Haemocyte apoptosis as a general cellular immune response of the snail, Lymnaea stagnalis, to a toxicant. | 2007-05 |
|
| Hemocyte-specific responses to the peroxidizing herbicide fomesafen in the pond snail Lymnaea stagnalis (Gastropoda, Pulmonata). | 2007-03 |
|
| Use of carbon and nitrogen stable isotope ratios to assess the effects of environmental contaminants on aquatic food webs. | 2006-05 |
|
| Effects of self-fertilization, environmental stress and exposure to xenobiotics on fitness-related traits of the freshwater snail Lymnaea stagnalis. | 2006-03 |
|
| Homoglutathione confers tolerance to acifluorfen in transgenic tobacco plants expressing soybean homoglutathione synthetase. | 2005-08 |
|
| Manipulation of plant tolerance to herbicides through co-ordinated metabolic engineering of a detoxifying glutathione transferase and thiol cosubstrate. | 2005-07 |
|
| Effects of fomesafen, alone and in combination with an adjuvant, on plankton communities in freshwater outdoor pond mesocosms. | 2005-05 |
|
| Population dynamics of weeds in no-tillage and conventional crop systems. | 2005 |
|
| Multiple resistance of acetolactate synthase and protoporphyrinogen oxidase inhibitors in Euphorbia heterophylla biotypes. | 2005 |
|
| Quantitative expression analysis of GH3, a gene induced by plant growth regulator herbicides in soybean. | 2004-02-11 |
|
| Experimental hepatic uroporphyria induced by the diphenyl-ether herbicide fomesafen in male DBA/2 mice. | 2003-05-15 |
|
| ZnCl2 induces Syrian hamster embryo (SHE) cell transformation. | 2003-04-30 |
|
| Solid-phase fluoroimmunoassay for the determination of mesotrione--a novel triketone herbicide--in water with direct measurement of the fluorescence onto the solid support. | 2003-04 |
|
| Circadian response of annual weeds in a natural setting to high and low application rates of four herbicides with different modes of actions. | 2003-03 |
|
| Nonylphenol polyethoxylate adjuvant mitigates the reproductive toxicity of fomesafen on the freshwater snail Lymnaea stagnalis in outdoor experimental ponds. | 2002-09 |
|
| [Participation of dexamethasone and E and C vitamins in the modulation of the hepatotoxic effect induced by fomesafen and 2,4-D amino herbicides, in rats ]. | 2002 |
|
| The effect of protoporphyrinogen oxidase inhibitors on microsomal and mitochondrial cytochromes. | 1995-12 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 23:24:59 GMT 2025
by
admin
on
Mon Mar 31 23:24:59 GMT 2025
|
| Record UNII |
T0SNA1AMVA
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
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Common Name | English | ||
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Preferred Name | English | ||
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| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
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EPA PESTICIDE CODE |
123802
Created by
admin on Mon Mar 31 23:24:59 GMT 2025 , Edited by admin on Mon Mar 31 23:24:59 GMT 2025
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| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
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fomesafen-sodium
Created by
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108731-70-0
Created by
admin on Mon Mar 31 23:24:59 GMT 2025 , Edited by admin on Mon Mar 31 23:24:59 GMT 2025
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60267
Created by
admin on Mon Mar 31 23:24:59 GMT 2025 , Edited by admin on Mon Mar 31 23:24:59 GMT 2025
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138164
Created by
admin on Mon Mar 31 23:24:59 GMT 2025 , Edited by admin on Mon Mar 31 23:24:59 GMT 2025
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DTXSID1034921
Created by
admin on Mon Mar 31 23:24:59 GMT 2025 , Edited by admin on Mon Mar 31 23:24:59 GMT 2025
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T0SNA1AMVA
Created by
admin on Mon Mar 31 23:24:59 GMT 2025 , Edited by admin on Mon Mar 31 23:24:59 GMT 2025
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m5524
Created by
admin on Mon Mar 31 23:24:59 GMT 2025 , Edited by admin on Mon Mar 31 23:24:59 GMT 2025
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PRIMARY | Merck Index |