Spirodiclofen
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| Names | |
|---|---|
| Preferred IUPAC name
3-(2,4-Dichlorophenyl)-2-oxo-1-oxaspiro[4.5]non-3-en-4-yl 2,2-dimethylbutanoate | |
| Identifiers | |
3D model (JSmol)
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| ChEMBL | |
| ChemSpider | |
| ECHA InfoCard | Lua error in Module:Wikidata at line 880: attempt to index field 'wikibase' (a nil value). Lua error in Module:Wikidata at line 880: attempt to index field 'wikibase' (a nil value).Lua error in Module:EditAtWikidata at line 29: attempt to index field 'wikibase' (a nil value). |
| EC Number |
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| E number | Lua error in Module:Wikidata at line 880: attempt to index field 'wikibase' (a nil value). |
| KEGG | |
PubChem CID
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| UNII | |
CompTox Dashboard (EPA)
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| Properties | |
| C21H24Cl2O4 | |
| Molar mass | 411.32 g·mol−1 |
| Appearance | White solid |
| Melting point | 94.8 °C (202.6 °F; 367.9 K)[1] |
| Hazards | |
| GHS labelling: | |
| GHS07: Exclamation markGHS08: Health hazardGHS09: Environmental hazard | |
| Danger | |
| H317, H350, H361, H373, H410 | |
| P201, P202, P260, P261, P272, P273, P280, P281, P302+P352, P308+P313, P314, P321, P333+P313, P363, P391, P405, P501 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Spirodiclofen is an acaricide and insecticide used in agriculture to control mites and San Jose scale. In the United States, it is used on citrus, grapes, pome fruit, stone fruit, and tree nut crops.[1][2][3]
Spirodiclofen belongs to the tetronic acid class and acts by inhibiting lipid biosynthesis, specifically acetyl CoA carboxylase, and is in IRAC group 23.[3][4]
References
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