Fomesafen structure
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Common Name | Fomesafen | ||
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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 |
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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]. |
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Related Catalog | |
References |
Density | 1.6±0.1 g/cm3 |
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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 |
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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 |
~% Fomesafen CAS#:72178-02-0 |
Literature: US5952531 A1, ; |
~% Fomesafen CAS#:72178-02-0 |
Literature: US4388472 A1, ; |
Precursor 3 | |
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DownStream 0 |
HS Code | 2935009016 |
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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% |
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 |