Weight | 202.214 g/mol |
---|---|
Formula | C7H14N4O3 |
Hydrogen Acceptors | 4 |
Hydrogen Donors | 2 |
Aromatic Rings | 0 |
Rotatable Bonds | 3 |
Dinotefuran (165252-70-0)
Score:
#1802 in Biology
,
#2146 in Chemistry
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- Sigma-Aldrich - Dinotefuran255.50 USD
- Fisher Scientific - Search for Dinotefuran
- TCI - Search for Dinotefuran
- Dinotefuran: A Potential Neonicotinoid Insecticide Against Resistant Mosquitoes (Journal of Medical Entomology, 2004)
- The discovery of dinotefuran: a novel neonicotinoid. (Pest Management Science, 2003)
- Unique and common metabolites of thiamethoxam, clothianidin, and dinotefuran in mice. (Chemical Research in Toxicology, 2006)
- Structural effects of dinotefuran and analogues in insecticidal and neural activities (Pest Management Science, 2002)
- Interaction of dinotefuran and its analogues with nicotinic acetylcholine receptors of cockroach nerve cords (Pest Management Science, 2002)
- Analytical evaluation of enzyme-linked immunosorbent assay for neonicotinoid dinotefuran for potential application to quick and simple screening method in rice samples. (Talanta, 2011)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCN=C(NCC1CCOC1)N[N+](=O)[O-]
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InChIKeyYKBZOVFACRVRJN-UHFFFAOYSA-N
- Pubchem - Dinotefuran
- Wikipedia - dinotefuran
Dinotefuran is an insecticide of the neonicotinoid class developed by Mitsui Chemicals for control of insect pests such as aphids, whiteflies, thrips, leafhoppers, leafminers, sawflies, mole cricket, white grubs, lacebugs, billbugs, beetles, mealybugs, and cockroaches on leafy vegetables, in residential and commercial buildings, and for professional turf management. Its mechanism of action involves disruption of the insect's nervous system by inhibiting nicotinic acetylcholine receptors. In order to avoid harming beneficial insects such as bees, it should not be applied during bloom.
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Nitramide
(Thiourea)
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