![]() | |
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)
|
|
ChEBI | |
ChEMBL | |
ChemSpider | |
ECHA InfoCard | 100.130.204 |
EC Number |
|
KEGG | |
PubChem
CID
|
|
UNII | |
CompTox Dashboard (
EPA)
|
|
| |
| |
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: | |
![]() ![]() ![]() | |
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).
|
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]
Spirodiclofen belongs to the tetronic acid class and acts by inhibiting lipid biosynthesis. [3]
![]() | |
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)
|
|
ChEBI | |
ChEMBL | |
ChemSpider | |
ECHA InfoCard | 100.130.204 |
EC Number |
|
KEGG | |
PubChem
CID
|
|
UNII | |
CompTox Dashboard (
EPA)
|
|
| |
| |
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: | |
![]() ![]() ![]() | |
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).
|
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]
Spirodiclofen belongs to the tetronic acid class and acts by inhibiting lipid biosynthesis. [3]