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succinate dehydrogenase inhibitor
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| Names | |
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IUPAC name 2’-[1,1’-bicycloprop-2-yl]-3-(difluoromethyl)-1-methylpyrazole-4-carboxanilide | |
| Other names SYN524464 | |
| Identifiers | |
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3D model (JSmol) |
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ChemSpider |
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ECHA InfoCard | 100.214.982 |
PubChem CID |
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{{{1}}} |
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| Properties | |
Chemical formula | C18H19F2N3O |
Molar mass | 7002331367000000000♠331.367 g·mol−1 |
| Appearance | White powder[1] |
Odor | Odorless[1] |
Density | 1.23 g/cm3 (26 °C)[1] |
Melting point | 121.4 °C (250.5 °F; 394.5 K)[1] |
Solubility in water | Very slightly soluble (0.67 g/L, 20 °C)[1] |
Solubility in other solvents | Slightly soluble in acetone (410 g/L) and dichloromethane (500 g/L)[1] |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
Infobox references | |
Sedaxane is a chemical developed as a fungicide in the European Union.
The molecular grouping to which it belongs is a pyrazole-4-carboxylic acid amide; its method of action is as a succinate dehydrogenase inhibitor (SDI).[2]
It is approved in Austria, and pending approval in Germany and Switzerland.
References
^ abcdef William Donovan. "Sedaxane" (PDF). United States Environmental Protection Agency..mw-parser-output cite.citation{font-style:inherit}.mw-parser-output .citation q{quotes:"""""""'""'"}.mw-parser-output .citation .cs1-lock-free a{background:url("//upload.wikimedia.org/wikipedia/commons/thumb/6/65/Lock-green.svg/9px-Lock-green.svg.png")no-repeat;background-position:right .1em center}.mw-parser-output .citation .cs1-lock-limited a,.mw-parser-output .citation .cs1-lock-registration a{background:url("//upload.wikimedia.org/wikipedia/commons/thumb/d/d6/Lock-gray-alt-2.svg/9px-Lock-gray-alt-2.svg.png")no-repeat;background-position:right .1em center}.mw-parser-output .citation .cs1-lock-subscription a{background:url("//upload.wikimedia.org/wikipedia/commons/thumb/a/aa/Lock-red-alt-2.svg/9px-Lock-red-alt-2.svg.png")no-repeat;background-position:right .1em center}.mw-parser-output .cs1-subscription,.mw-parser-output .cs1-registration{color:#555}.mw-parser-output .cs1-subscription span,.mw-parser-output .cs1-registration span{border-bottom:1px dotted;cursor:help}.mw-parser-output .cs1-ws-icon a{background:url("//upload.wikimedia.org/wikipedia/commons/thumb/4/4c/Wikisource-logo.svg/12px-Wikisource-logo.svg.png")no-repeat;background-position:right .1em center}.mw-parser-output code.cs1-code{color:inherit;background:inherit;border:inherit;padding:inherit}.mw-parser-output .cs1-hidden-error{display:none;font-size:100%}.mw-parser-output .cs1-visible-error{font-size:100%}.mw-parser-output .cs1-maint{display:none;color:#33aa33;margin-left:0.3em}.mw-parser-output .cs1-subscription,.mw-parser-output .cs1-registration,.mw-parser-output .cs1-format{font-size:95%}.mw-parser-output .cs1-kern-left,.mw-parser-output .cs1-kern-wl-left{padding-left:0.2em}.mw-parser-output .cs1-kern-right,.mw-parser-output .cs1-kern-wl-right{padding-right:0.2em}
^ Ronald Zeun, Gabriel Scalliet and Michael Oostendorp (2013). "Biological activity of sedaxane - a novel broad-spectrum fungicide for seed treatment" (PDF). Pest Management Science. 69 (4): 527–534. doi:10.1002/ps.3405.
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