| Identification | Back Directory | [Name]
ethyl 2-[[4-chloro-6-(propan-2-ylamino)-1,3,5-triazin-2-yl]amino]aceta te | [CAS]
68228-18-2 | [Synonyms]
MG-07
Proglinazine-ethyl
N-(4-Chloro-6-isopropylamino-1,3,5-triazin-2-yl)glycine ethyl ester
ethyl 2-[[4-chloro-6-(propan-2-ylamino)-1,3,5-triazin-2-yl]amino]aceta te
Glycine, N-[4-chloro-6-[(1-methylethyl)amino]-1,3,5-triazin-2-yl]-, ethyl ester | [Molecular Formula]
C10H16ClN5O2 | [MOL File]
68228-18-2.mol | [Molecular Weight]
273.72 |
| Hazard Information | Back Directory | [Production Methods]
Proglinazine was produced through a manufacturing sequence typical of substituted triazinone chemistry. Industrial routes generally began with cyanuric chloride, which was subjected to stepwise nucleophilic substitution: first with an appropriate amine to introduce the primary side chain, then with a secondary amine or heterocycle to complete the substitution pattern that defines proglinazine’s herbicidal structure. Each substitution step required careful temperature control to ensure selectivity among the three chlorine atoms on the triazine ring. After neutralisation and isolation of this intermediate, the ethyl ester functionality was installed by reacting the appropriate carboxylate or acylating agent with the remaining reactive site on the triazinone framework. | [Mechanism of action]
Photosynthetic electron transport inhibitor at the photosystem II receptor site, Selective | [Pesticide Type]
Herbicide |
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