| Identification | Back Directory | [Name]
Carbonic acid, butyl 3-(2,4-dichlorophenyl)-2-oxo-1-oxaspiro[4.5]dec-3-en-4-yl ester | [CAS]
1305319-70-3 | [Synonyms]
Spirobudiclofen
Carbonic acid, butyl 3-(2,4-dichlorophenyl)-2-oxo-1-oxaspiro[4.5]dec-3-en-4-yl ester | [Molecular Formula]
C20H22Cl2O5 | [MOL File]
1305319-70-3.mol | [Molecular Weight]
413.29 |
| Chemical Properties | Back Directory | [Boiling point ]
560.8±50.0 °C(Predicted) | [density ]
1.33±0.1 g/cm3(Predicted) | [solubility ]
Chloroform (Slightly), Methanol (Slightly, Heated) | [form ]
Solid | [color ]
White to Off-White |
| Hazard Information | Back Directory | [Uses]
Butyl 3-(2,4-dichlorophenyl)-2-oxo-1-oxaspiro[4.5]dec-3-en-4-yl carbonate(cas# 1305319-70-3) is used in agricultural studies based on active compound combinations comprising fatty acids. Acaricide related to Spirodiclofen (S682990) | [Definition]
ChEBI: Spirobudifen is an oxaspiro compound that is 1-oxaspiro[4.5]dec-3-en-2-one substituted by 2,4-dichlorophenyl and (butoxycarbonyl)oxy groups at positions 3 and 4, respectively. It is an acaricide from Zhejiang Udragon Bioscience. It is a dichlorobenzene, an oxaspiro compound, an organochlorine acaricide and a carbonate ester. | [Production Methods]
Although no public source provides a full industrial manufacturing description for spirobudifen, its structure and class make the commercial route clear: production centers on constructing the tetronic acid core, followed by spiro fusion with a substituted cycloalkenone, and final esterification to introduce the butoxycarbonyl group. The 2,4 dichlorophenyl moiety is incorporated via electrophilic substitution or coupling chemistry typical of modern acaricide synthesis. | [Mechanism of action]
Selective, non-systemic, distrupts mite development. Acetyl CoA carboxylase inhibitor (ACCase) - distrupts fatty acid biosynthesis and lipid formation. | [Pesticide Type]
Insecticide; Acaricide |
|
|