| Identification | Back Directory | [Name]
Methanesulfonamide, N-[2-[(3,3-dimethyl-2-oxo-1-azetidinyl)methyl]phenyl]-1,1,1-trifluoro- | [CAS]
1215111-77-5 | [Synonyms]
N-{2-[(3,3-dimethyl-2-oxoazetidin-1-yl)methyl]phenyl}-1,1,1-trifluoromethanesulfonamide
Methanesulfonamide, N-[2-[(3,3-dimethyl-2-oxo-1-azetidinyl)methyl]phenyl]-1,1,1-trifluoro- | [Molecular Formula]
C13H15F3N2O3S | [MDL Number]
MFCD34168500 | [MOL File]
1215111-77-5.mol | [Molecular Weight]
336.33 |
| Hazard Information | Back Directory | [Production Methods]
Dimesulfazet is manufactured through an industrial sequence that assembles its sulfonyl-triazinone framework and substituted aromatic ring system under conditions designed to tightly control regioselectivity and sulphur-based impurities. Producers typically begin by constructing the heterocyclic triazinone core from an appropriate urea or guanidine precursor, followed by chlorination or other activation steps that prepare the ring for nucleophilic substitution. In parallel, the substituted phenylsulfonyl fragment is generated through controlled sulfonation and halogenation, then converted to a reactive sulfonyl chloride or equivalent. The key bond-forming stage is the coupling of this activated sulfonyl intermediate with the triazinone nucleus under anhydrous, base-mediated conditions that suppress over sulfonylation and decomposition of the heterocycle. | [Mechanism of action]
Inhibition of very long chain fatty acids (VLCFA, inhibition of cell division) | [Pesticide Type]
Herbicide |
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