| Weight | 332.139 g/mol |
|---|---|
| Formula | C13H11Cl2NO5 |
| Hydrogen Acceptors | 5 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 3 |
CHLOZOLINATE (84332-86-5, 72391-46-9)
dichlozolinate
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- Administration of potentially antiandrogenic pesticides (procymidone, linuron, iprodione, chlozolinate, p,p-DDE, and ketoconazole) and toxic substances (dibutyl- and diethylhexyl phthalate, PCB 169, and ethane dimethane sulphonate) during sexual differentiation produces diverse profiles of reproductive malformations in the male rat (Toxicology and Industrial Health, 1999)
- Reversed-phase high-performance liquid chromatography of pesticides. VII: Analysis of vinclozolin, iprodione, procymidone, dichlozolinate and their degradation product 3,5-dichloroaniline on white must and wine extracts (Journal of Chromatography A, 1983)
- Chlozolinate fate during vinification process (Journal of Agricultural and Food Chemistry, 1992)
- Degradation of dicarboximidic fungicides in wine. Part II: Isolation and identification of the major breakdown products of chlozolinate, vinclozolin and procymidone (Pesticide Science, 1986)
- Asymmetric synthesis of (R)-()-chlozolinate through a chemoenzymatic procedure (Tetrahedron-asymmetry, 2001)
- Residue Analysis of Imazapyr and Chlozolinate in Water Using Sunlight (Bulletin of Environmental Contamination and Toxicology, 1999)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H351: Suspected of causing cancer
Warning Carcinogenicity - Category 2 - dichlozolinate
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SMILESCCOC(=O)C1(C(=O)N(C(=O)O1)C2=CC(=CC(=C2)Cl)Cl)C
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InChIKeyIGUYEXXAGBDLLX-UHFFFAOYSA-N
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CHLOZOLINATE
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