| Weight | 216.198 g/mol |
|---|---|
| Formula | C8H9O3PS |
| Hydrogen Acceptors | 4 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
Salithion
90293-10-0, 3811-49-2, 90293-16-6
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- Synthesis of Highly Pure Enantiomers of the Insecticide Salithion (Agricultural and biological chemistry, 1989)
- Separation and toxicity of salithion enantiomers. (Chirality, 2009)
- Effect of Salithion Enantiomers on Larval Growth, Carbohydrases, Acetylcholinesterase, Adenylate Cyclase Activities and Cyclic Adenosine 3,5-monophosphate Level of Musca domestica and Tribolium castaneum (Agricultural and biological chemistry, 1990)
- Biological Activity of Optically Active Salithion and Salioxon (Agricultural and biological chemistry, 1989)
- Effect of salithion enantiomers on the trehalase system and on the digestive protease, amylase, and invertase of Tribolium castaneum (Pesticide Biochemistry and Physiology, 1989)
- Stereoselective degradation of organophosphorus insecticide salithion in upland soils (Journal of Pesticide Science, 1991)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H301: Toxic if swallowed
Danger Acute toxicity, oral - Category 3 - H370: Causes damage to organs
Danger Specific target organ toxicity, single exposure - Category 1 -
SMILESCOP1(=S)OCC2=CC=CC=C2O1
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InChIKeyOUNSASXJZHBGAI-UHFFFAOYSA-N
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