| Weight | 295.77 g/mol |
|---|---|
| Formula | C14H18ClN3O2 |
| Hydrogen Acceptors | 5 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 4 |
TRIADIMENOL
triadimefon · Bayleton · azocene
55219-65-3, 70585-35-2, 89482-17-7, 89497-63-2
Score:
#1397 in Biology
,
#1634 in Chemistry
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- Triadimefon induced changes in the antioxidant metabolism and ajmalicine production in Catharanthus roseus (L.) G. Don. (Plant Science, 2006)
- Effect of triadimefon and triadimenol on growth of various plant species as well as on gibberellin content and sterol metabolism in shoots of barley seedlings (Pesticide Biochemistry and Physiology, 1981)
- Triadimefon Protects Bean Plants from Water Stress through its Effects on Abscisic Acid (Plant and Cell Physiology, 1986)
- Comparative activity of the enantiomers of triadimenol and paclobutrazol as inhibitors of fungal growth and plant sterol and gibberellin biosynthesis (Pesticide Science, 1987)
- Distributions of Sensitivities to Three Sterol Demethylation Inhibitor Fungicides Among Populations of Uncinula necator Sensitive and Resistant to Triadimefon. (Phytopathology, 1997)
- Triadimefon induced salt stress tolerance in Withania somnifera and its relationship to antioxidant defense system (South African Journal of Botany, 2008)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - triadimefon
- Bayleton
- azocene
- triadimefon nitrate
- 1-(1,2,4-triazolyl)-1-(4-chlorophenoxy)-3,3-dimethylbutan-2-one
- triadimefon sulfate
- Tripinacloraz
-
SMILESCC(C)(C)C(C(N1C=NC=N1)OC2=CC=C(C=C2)Cl)O
-
InChIKeyBAZVSMNPJJMILC-UHFFFAOYSA-N
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