| Weight | 401.422 g/mol |
|---|---|
| Formula | C15H16F5NO2S2 |
| Hydrogen Acceptors | 5 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 5 |
Dithiopyr (97886-45-8)
Score:
#12 in i
,
#5132 in Chemistry
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- Effects of the herbicide dithiopyr on cell division in wheat root tips (Pesticide Biochemistry and Physiology, 1991)
- Turf Safety and Effectiveness of Dithiopyr and Quinclorac for Large Crabgrass (Digitaria sanguinalis) Control in Spring-Seeded Turf" (Weed Technology, 1999)
- Efficacy and dissipation of dithiopyr and pendimethalin in perennial ryegrass (Lolium perenne) turf (Weed Science, 1995)
- Potential Movement of Dithiopyr following Application to Golf Courses (Journal of Environmental Quality, 1997)
- Abiotic and Biotic Degradation of Dithiopyr in Golf Course Greens (Journal of Agricultural and Food Chemistry, 1996)
- Immunofluorescence and electron microscopic investigations of the effects of dithiopyr on onion root tips (Pesticide Biochemistry and Physiology, 1991)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC(C)CC1=C(C(=NC(=C1C(=O)SC)C(F)(F)F)C(F)F)C(=O)SC
-
InChIKeyYUBJPYNSGLJZPQ-UHFFFAOYSA-N
- Pubchem - Dithiopyr
- Wikipedia - dithiopyr
Dithiopyr is a preemergent herbicide for crabgrass control in turf and ornamental grasses. It is effective on 45 grassy and broadleaf weeds. Dithiopyr inhibits root growth of susceptible weeds as well as turf grass and thus should be used only on established turf with a well-developed root system.
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Synthesis
Reactant
+
1-Chloro-2-methylpropane
(Friedel-Crafts alkylation)
Reactant
+
dimethyl sulfide
(Corey-Kim oxidation of secondary alcohols)
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