| Weight | 291.782 g/mol |
|---|---|
| Formula | C15H18ClN3O |
| Hydrogen Acceptors | 4 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 5 |
Cyproconazole (94361-06-5)
Score:
#11 in Botany
,
#141 in Environmental science
,
#1756 in Biology
,
#2075 in Chemistry
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- Influence of pH on the stereoselective degradation of the fungicides epoxiconazole and cyproconazole in soils. (Environmental Science & Technology, 2006)
- Selection for increased cyproconazole tolerance in Mycosphaerella graminicola through local adaptation and in response to host resistance (Molecular Plant Pathology, 2006)
- Photocatalytic degradation of a triazole pesticide, cyproconazole, in water (Journal of Photochemistry and Photobiology A-chemistry, 2007)
- Mouse Liver Effects of Cyproconazole, a Triazole Fungicide: Role of the Constitutive Androstane Receptor (Toxicological Sciences, 2007)
- Transcriptomic concentration-response evaluation of valproic acid, cyproconazole, and hexaconazole in the neural embryonic stem cell test (ESTn). (Toxicological Sciences, 2012)
- Developmental toxicity of cyproconazole, an inhibitor of fungal ergosterol biosynthesis, in the rat. (Bulletin of Environmental Contamination and Toxicology, 1995)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H302: Harmful if swallowed
Warning Acute toxicity, oral - Category 4 - H400: Very toxic to aquatic life
Warning Hazardous to the aquatic environment, acute hazard - Category 1 - H410: Very toxic to aquatic life with long lasting effects
Warning Hazardous to the aquatic environment, long-term hazard - Category 1 -
SMILESCC(C1CC1)C(CN2C=NC=N2)(C3=CC=C(C=C3)Cl)O
-
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- Pubchem - Cyproconazole
- Wikipedia - 2-(4-chlorophenyl)-3-cyclopropyl-1-(1H-1,2,4-triazol-1-yl)butan-2-ol
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