Fomesafen structure
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Common Name | Fomesafen | ||
|---|---|---|---|---|
| CAS Number | 72178-02-0 | Molecular Weight | 438.763 | |
| Density | 1.6±0.1 g/cm3 | Boiling Point | 531.4±60.0 °C at 760 mmHg | |
| Molecular Formula | C15H10ClF3N2O6S | Melting Point | 220-221°C | |
| MSDS | Chinese USA | Flash Point | 275.2±32.9 °C | |
| Symbol |
GHS07 |
Signal Word | Warning | |
Use of FomesafenFomesafen is a type of efficient and selective protoporphyrinogen IX oxidase (PPO) inhibitor. Fomesafen is a herbicide and has the advantages of low toxicity and high selectivity[1]. |
| Name | fomesafen |
|---|---|
| Synonym | More Synonyms |
| Description | Fomesafen is a type of efficient and selective protoporphyrinogen IX oxidase (PPO) inhibitor. Fomesafen is a herbicide and has the advantages of low toxicity and high selectivity[1]. |
|---|---|
| Related Catalog | |
| References |
| Density | 1.6±0.1 g/cm3 |
|---|---|
| Boiling Point | 531.4±60.0 °C at 760 mmHg |
| Melting Point | 220-221°C |
| Molecular Formula | C15H10ClF3N2O6S |
| Molecular Weight | 438.763 |
| Flash Point | 275.2±32.9 °C |
| Exact Mass | 437.990021 |
| PSA | 126.67000 |
| LogP | 3.58 |
| Vapour Pressure | 0.0±1.5 mmHg at 25°C |
| Index of Refraction | 1.586 |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
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| Symbol |
GHS07 |
|---|---|
| Signal Word | Warning |
| Hazard Statements | H302 |
| Personal Protective Equipment | dust mask type N95 (US);Eyeshields;Gloves |
| Hazard Codes | Xn:Harmful |
| Risk Phrases | R22 |
| Safety Phrases | S2 |
| RIDADR | NONH for all modes of transport |
| RTECS | CV2475000 |
| HS Code | 2935009016 |
|
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Fomesafen CAS#:72178-02-0 |
| Literature: US5952531 A1, ; |
|
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Fomesafen CAS#:72178-02-0 |
| Literature: US4388472 A1, ; |
| Precursor 3 | |
|---|---|
| DownStream 0 | |
| HS Code | 2935009016 |
|---|---|
| Summary | 2935009016 methyl (4-aminophenyl)sulfonylcarbamate。supervision conditions:s(import or export registration certificate for pesticides)。VAT:17.0%。tax rebate rate:9.0%。MFN tarrif:6.5%。general tariff:35.0% |
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The effect of protoporphyrinogen oxidase inhibitors on microsomal and mitochondrial cytochromes.
Obes. Res. 3 Suppl 5 , 785S-788S, (1995) Neurological dysfunction is a characteristic feature of acute porphyrias, unexplained until now. One of the possible explanations is a deficiency of heme in the central nervous system, caused by a blo... |
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Occurrence and distribution of sulfonylurea and related herbicides in central Canadian surface waters 2006-2008.
Bull. Environ. Contam. Toxicol. 87(4) , 420-5, (2011) Surface water sampling in 2006-2008 measured the occurrence of sulfonylureas and related herbicides (SUs) during base flow conditions and wet weather events. Flumetsulam (29.2%), diuron (36.5%) and fo... |
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Experimental hepatic uroporphyria induced by the diphenyl-ether herbicide fomesafen in male DBA/2 mice.
Toxicol. Appl. Pharmacol. 189(1) , 28-38, (2003) Hepatic uroporphyria can be readily induced by a variety of treatments in mice of the C57BL strains, whereas DBA/2 mice are almost completely resistant. However, feeding of the protoporphyrinogen oxid... |
| 5-[2-chloro-4-(trifluoromethyl)phenoxy]-N-(methanesulfonyl)-2-nitrobenzamide |
| Benzamide, 5-[2-chloro-4-(trifluoromethyl)phenoxy]-N-(methylsulfonyl)-2-nitro- |
| 5-[2-chloro-4-(trifluoromethyl)phenoxy]-N-methylsulfonyl-2-nitrobenzamide |
| Benzenecarboximidic acid, 5-[2-chloro-4-(trifluoromethyl)phenoxy]-N-(methylsulfonyl)-2-nitro- |
| MFCD01632756 |
| EINECS 276-439-9 |
| 5-[2-Chloro-4-(trifluoromethyl)phenoxy]-N-(methylsulfonyl)-2-nitrobenzenecarboximidic acid |
| 5-(2-chloro-α,α,α-trifluoro-p-tolyloxy)-N-mesyl-2-nitrobenzamide |
| fomesafen [ANSI] |
| Fomesafen |
| 5-[2-Chloro-4-(trifluoromethyl)phenoxy]-N-(methylsulfonyl)-2-nitrobenzamide |
| WS1&MVR BNW EOR BG DXFFF |
| Fomesafene |