| Identification | Back Directory | [Name]
1H-Pyrazole-4-carboxylic acid, 5-chloro-1,3-dimethyl-, 4-[2-chloro-3-[(5-methyl-2-oxo-1,3,4-oxadiazol-3(2H)-yl)methyl]-4-(methylsulfonyl)benzoyl]-3-cyclopropyl-1-methyl-1H-pyrazol-5-yl ester | [CAS]
3023924-34-4 | [Synonyms]
1H-Pyrazole-4-carboxylic acid, 5-chloro-1,3-dimethyl-, 4-[2-chloro-3-[(5-methyl-2-oxo-1,3,4-oxadiazol-3(2H)-yl)methyl]-4-(methylsulfonyl)benzoyl]-3-cyclopropyl-1-methyl-1H-pyrazol-5-yl ester | [Molecular Formula]
C25H24Cl2N6O7S | [MOL File]
3023924-34-4.mol | [Molecular Weight]
623.47 |
| Hazard Information | Back Directory | [Production Methods]
Prochlorosulfone is synthesised through a multi-step condensation process. Commercial production begins with the preparation of a substituted benzoyl chloride, which is reacted with a methylsulfonyl group and a chloro-substituted aromatic ring. This intermediate is then coupled with heterocyclic components, specifically a pyrazole derivative and an oxadiazolone fragment, using controlled acylation and esterification reactions. The process requires precise temperature and pH control to maintain stereochemistry (typically the (1R,3R)-cyclopropyl configuration) for optimal herbicidal activity. After assembly of the full molecule, the product undergoes purification and crystallisation to achieve technical-grade purity suitable for formulation. | [Mechanism of action]
Bleaching: inhibition of 4-hydroxyphenyl-pyruvate-dioxygenase. | [Pesticide Type]
Herbicide |
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