| Weight | 216.668 g/mol |
|---|---|
| Formula | C9H13ClN2O2 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
TERBACIL (5902-51-2)
terbacil monolithium salt · 3-tert-butyl-5-chloro-6-methyluracil · terbacyl
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- Semiconductor-mediated photocatalyzed degradation of two selected pesticide derivatives, terbacil and 2,4,5-tribromoimidazole, in aqueous suspension (Applied Catalysis B-environmental, 2002)
- Synthesis and studies with labeled bromacil 2-C14 and terbacil. (Journal of Agricultural and Food Chemistry, 1969)
- Thinning of Spur `Delicious' Apples by Shade, Terbacil, Carbaryl, and Ethephon (Journal of The American Society for Horticultural Science, 1990)
- Persistence of terbacil and trifluralin under different soil and climatic conditions (Weed Research, 1977)
- Movement and persistence of imazaquin, oxyfluorfen, flurochloridone and terbacil in soil (Weed Research, 1996)
- Identification of the metabolites of terbacil in dog urine. (Journal of Agricultural and Food Chemistry, 1969)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - terbacil monolithium salt
- 3-tert-butyl-5-chloro-6-methyluracil
- terbacyl
-
SMILESCC1=C(C(=O)N(C(=O)N1)C(C)(C)C)Cl
-
InChIKeyNBQCNZYJJMBDKY-UHFFFAOYSA-N
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