| Identification | Back Directory | [Name]
Benzenesulfonamide, 2-iodo-N-[[(4-methoxy-6-methyl-1,3,5-triazin-2-yl)amino]carbonyl]- | [CAS]
1144097-22-2 | [Synonyms]
Benzenesulfonamide, 2-iodo-N-[[(4-methoxy-6-methyl-1,3,5-triazin-2-yl)amino]carbonyl]- | [Molecular Formula]
C12H12IN5O4S | [MOL File]
1144097-22-2.mol | [Molecular Weight]
449.22 |
| Hazard Information | Back Directory | [Production Methods]
Iofensulfuron is produced commercially through a sulfonylurea-type synthetic route that builds its pyrimidinylsulfonylurea herbicide framework. Industrial synthesis begins with preparation of a trifluoromethyl-substituted pyrimidine intermediate, which is functionalised via chlorination and subsequent substitution to introduce the sulfonyl group. In parallel, a phenylurea fragment is generated from aniline derivatives through carbamoylation. These two fragments are then coupled under controlled conditions to form the sulfonylurea linkage, yielding the final iofensulfuron structure. The process requires careful control of halogenation and condensation steps to ensure selectivity and high yield. | [Mechanism of action]
Inhibitor of acetolactate synthase which reduces plant shoot and root growth | [Pesticide Type]
Herbicide |
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