| Weight | 192.001 g/mol |
|---|---|
| Formula | C6H3Cl2NO2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
2,6-Dichloroisonicotinic acid (5398-44-7)
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- Inhibition of ascorbate peroxidase by salicylic acid and 2,6-dichloroisonicotinic acid, two inducers of plant defense responses (Proceedings of the National Academy of Sciences of the United States of America, 1995)
- 2,6-Dichloroisonicotinic acid-induced resistance to pathogens without the accumulation of salicylic acid (Molecular Plant-microbe Interactions, 1995)
- Acquired Resistance in Barley (The Resistance Mechanism Induced by 2,6-Dichloroisonicotinic Acid Is a Phenocopy of a Genetically Based Mechanism Governing Race-Specific Powdery Mildew Resistance) (Plant Physiology, 1994)
- Effect of treating soybean with 2,6-dichloroisonicotinic acid (INA) and benzothiadiazole (BTH) on seed yields and the level of disease caused by Sclerotinia sclerotiorum in field and greenhouse studies (European Journal of Plant Pathology, 1998)
- Gene-Expression Patterns and Levels of Jasmonic Acid in Rice Treated with the Resistance Inducer 2,6-Dichloroisonicotinic Acid (Plant Physiology, 1997)
- Induction of tomato stress protein mRNAs by ethephon, 2,6-dichloroisonicotinic acid and salicylate (Plant Molecular Biology, 1995)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=C(C=C(N=C1Cl)Cl)C(=O)O
-
InChIKeySQSYNRCXIZHKAI-UHFFFAOYSA-N
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2,6-Dichloroisonicotinic acid
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