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| Formula | C10H5Cl2NO2 |
| Net Charge | 0 |
| Average Mass | 242.061 |
| Monoisotopic Mass | 240.96973 |
| SMILES | O=C(O)c1c(Cl)ccc2cc(Cl)cnc12 |
| InChI | InChI=1S/C10H5Cl2NO2/c11-6-3-5-1-2-7(12)8(10(14)15)9(5)13-4-6/h1-4H,(H,14,15) |
| InChIKey | FFSSWMQPCJRCRV-UHFFFAOYSA-N |
| Wikipedia |
|---|
| Roles Classification |
|---|
| Chemical Role: | Bronsted acid A molecular entity capable of donating a hydron to an acceptor (Brønsted base). |
| Biological Role: | synthetic auxin A synthetic compound exhibiting auxin activity. |
| Applications: | herbicide A substance used to destroy plant pests. agrochemical An agrochemical is a substance that is used in agriculture or horticulture. |
| ChEBI Ontology |
|---|
| Outgoing Relation(s) |
| quinclorac (CHEBI:81974) has role agrochemical (CHEBI:33286) |
| quinclorac (CHEBI:81974) has role herbicide (CHEBI:24527) |
| quinclorac (CHEBI:81974) has role synthetic auxin (CHEBI:26841) |
| quinclorac (CHEBI:81974) is a monocarboxylic acid (CHEBI:25384) |
| quinclorac (CHEBI:81974) is a organochlorine compound (CHEBI:36683) |
| quinclorac (CHEBI:81974) is a quinolinemonocarboxylic acid (CHEBI:26512) |
| quinclorac (CHEBI:81974) is conjugate acid of quinclorac(1−) (CHEBI:132178) |
| Incoming Relation(s) |
| quinclorac-methyl (CHEBI:132879) has functional parent quinclorac (CHEBI:81974) |
| quinclorac(1−) (CHEBI:132178) is conjugate base of quinclorac (CHEBI:81974) |
| IUPAC Name |
|---|
| 3,7-dichloroquinoline-8-carboxylic acid |
| Synonym | Source |
|---|---|
| 3,7-dichloro-8-quinolinecarboxylic acid | Alan Wood's Pesticides |
| Manual Xrefs | Databases |
|---|---|
| C18806 | KEGG COMPOUND |
| quinclorac | Alan Wood's Pesticides |
| Quinclorac | Wikipedia |
| 577 | PPDB |
| Registry Numbers | Sources |
|---|---|
| Reaxys:7761858 | Reaxys |
| CAS:84087-01-4 | KEGG COMPOUND |
| CAS:84087-01-4 | Alan Wood's Pesticides |
| CAS:84087-01-4 | ChemIDplus |
| Citations |
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