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| | 1-(4-chlorophenyl)-6-methyl-4-oxo-pyridazine-3-carboxylate Basic information |
| Product Name: | 1-(4-chlorophenyl)-6-methyl-4-oxo-pyridazine-3-carboxylate | | Synonyms: | 1-(4-chlorophenyl)-6-methyl-4-oxo-pyridazine-3-carboxylate;Fenridazon [iso];1-(4-chlorophenyl)-6-Methyl-4-oxo-1,4-dihydropyridazine-3-carboxylate;1-(4-Chlorophenyl)-1,4-dihydro-6-methyl-4-oxo-3-pyridazinecarboxylic acid;3-Pyridazinecarboxylic acid, 1-(4-chlorophenyl)-1,4-dihydro-6-methyl-4-oxo-;Butafenacil Impurity 8 | | CAS: | 68254-10-4 | | MF: | C12H9ClN2O3 | | MW: | 264.66 | | EINECS: | | | Product Categories: | | | Mol File: | 68254-10-4.mol |  |
| | 1-(4-chlorophenyl)-6-methyl-4-oxo-pyridazine-3-carboxylate Chemical Properties |
| Melting point | 234.3-235.1℃ (ethanol ) | | Boiling point | 453.4±47.0 °C(Predicted) | | density | 1.43±0.1 g/cm3(Predicted) | | pka | 0.17±0.20(Predicted) |
| | 1-(4-chlorophenyl)-6-methyl-4-oxo-pyridazine-3-carboxylate Usage And Synthesis |
| Production Methods | The commercial production of fenridazon involves the synthesis of a pyridazine-3-carboxylic acid derivative, specifically 1-(4-chlorophenyl)-6-methyl-4-oxo-1,4-dihydropyridazine-3-carboxylic acid. The process includes chlorination, methylation, and cyclization steps to form the pyridazine ring system, followed by carboxylation. | | Mechanism of action | A chemical hybridizing agent causing male floral sterility | | Pesticide Type | Plant Growth Regulator; Gametocide |
| | 1-(4-chlorophenyl)-6-methyl-4-oxo-pyridazine-3-carboxylate Preparation Products And Raw materials |
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