Epoxiconazole
Epoxiconazole structure
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Common Name | Epoxiconazole | ||
|---|---|---|---|---|
| CAS Number | 133855-98-8 | Molecular Weight | 329.756 | |
| Density | 1.4±0.1 g/cm3 | Boiling Point | 463.1±55.0 °C at 760 mmHg | |
| Molecular Formula | C17H13ClFN3O | Melting Point | 125°C (lit.) | |
| MSDS | Chinese USA | Flash Point | 233.9±31.5 °C | |
| Symbol |
GHS08, GHS09 |
Signal Word | Danger | |
Use of EpoxiconazoleEpoxiconazole, a fungicide, is a demethylation inhibitor of the Ergosterol biosynthesis pathway. Epoxiconazole exhibits strong inhibitory effects on both carbendazim-resistant and phenamacril-resistant isolates, and can be used for controlling many crop diseases[1]. |
| Name | 1-[[(2S,3R)-3-(2-chlorophenyl)-2-(4-fluorophenyl)oxiran-2-yl]methyl]-1,2,4-triazole |
|---|---|
| Synonym | More Synonyms |
| Description | Epoxiconazole, a fungicide, is a demethylation inhibitor of the Ergosterol biosynthesis pathway. Epoxiconazole exhibits strong inhibitory effects on both carbendazim-resistant and phenamacril-resistant isolates, and can be used for controlling many crop diseases[1]. |
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| Related Catalog | |
| References |
| Density | 1.4±0.1 g/cm3 |
|---|---|
| Boiling Point | 463.1±55.0 °C at 760 mmHg |
| Melting Point | 125°C (lit.) |
| Molecular Formula | C17H13ClFN3O |
| Molecular Weight | 329.756 |
| Flash Point | 233.9±31.5 °C |
| Exact Mass | 329.073120 |
| PSA | 43.24000 |
| LogP | 3.44 |
| Vapour Pressure | 0.0±1.1 mmHg at 25°C |
| Index of Refraction | 1.659 |
| Symbol |
GHS08, GHS09 |
|---|---|
| Signal Word | Danger |
| Hazard Statements | H351-H360Df-H411 |
| Precautionary Statements | P201-P273-P308 + P313-P391-P501 |
| Hazard Codes | Xn: Harmful;N: Dangerous for the environment; |
| Risk Phrases | R40;R51/53;R62;R63 |
| Safety Phrases | 36/37-46-61 |
| RIDADR | UN 3077 |
| RTECS | XZ4500100 |
| HS Code | 2933199090 |
| HS Code | 2933199090 |
|---|---|
| Summary | 2933199090. other compounds containing an unfused pyrazole ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |
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Molecular modelling of the emergence of azole resistance in Mycosphaerella graminicola.
PLoS ONE 6(6) , e20973, (2011) A structural rationale for recent emergence of azole (imidazole and triazole) resistance associated with CYP51 mutations in the wheat pathogen Mycosphaerella graminicola is presented, attained by homo... |
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Enantiomeric separation of triazole fungicides with 3-μm and 5-μml particle chiral columns by reverse-phase high-performance liquid chromatography.
Chirality 23(6) , 479-86, (2011) This study used chiral columns packed with 3-μm and 5-μm particles to comparatively separate enantiomers of 9 triazole fungicides, and Lux Cellulose-1 columns with chiral stationary phase of cellulose... |
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Inhibition of efflux transporter-mediated fungicide resistance in Pyrenophora tritici-repentis by a derivative of 4'-hydroxyflavone and enhancement of fungicide activity.
Appl. Environ. Microbiol. 71(6) , 3269-75, (2005) Populations of the causal agent of wheat tan spot, Pyrenophora tritici-repentis, that are collected from fields frequently treated with reduced fungicide concentrations have reduced sensitivity to str... |
| Opal 7.5 EC |
| 1-{[3-(2-Chlorphenyl)-2-(4-fluorphenyl)oxiran-2-yl]methyl}-1H-1,2,4-triazol |
| 1-[[3-(2-Chlorophenyl)-2-(4-fluorophenyl)oxiranyl]methyl]-1H-1,2,4-triazole |
| 1-{[3-(2-Chlorophenyl)-2-(4-fluorophenyl)-2-oxiranyl]methyl}-1H-1,2,4-triazole |
| 1H-1,2,4-Triazole, 1-[[3-(2-chlorophenyl)-2-(4-fluorophenyl)oxiranyl]methyl]- |
| OPUS |
| (2RS,3SR)-1-[3-(2-chlorophenyl)-2,3-epoxy-2-(4-fluorophenyl)propyl]-1H-1,2,4-triazole |
| Epoxiconazole |
| 1-{[3-(2-Chlorophenyl)-2-(4-fluorophenyl)oxiran-2-yl]methyl}-1H-1,2,4-triazole |