Synthesis and Herbicidal Activity of N-[5-(3-Methyl-2,6-dioxo-4-trifluoromethyl-2,3-dihydropyrimidin-1(6H)-yl) phenyl]-N',N'-disubstituted Urea Compounds
Mingzhi Huang
Abstract
Mingzhi Huang
Abstract
In search of safe and low toxin herbicidal compounds, seven N-[5-(3-methyl-2,6-dioxo-4- trifluoromethyl-2,3-dihydropyrimidin-1(6H)-yl)phenyl]-N',N'-disubstituted urea compounds were designed and synthesized. Their structures were confirmed by IR, 1H NMR, LC/MS and elemental analyses. Pre- liminary bioassay showed that most of title compounds had good herbicidal activity, for example, 4c-4f exhibited more than 90% inhibition to Abutilon theophrasti Medic, Amaranthus spinosus, Chenopodium album, Digitaria sanguinalis, Echinochloa crus-galli, and Setaria viridis at active ingredient 75 g a.i./hm2 in post-emergence treatment.
A significance statement is not available in the OpenAlex record.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
In search of safe and low toxin herbicidal compounds, seven N-[5-(3-methyl-2,6-dioxo-4- trifluoromethyl-2,3-dihydropyrimidin-1(6H)-yl)phenyl]-N',N'-disubstituted urea compounds were designed and synthesized. Their structures were confirmed by IR, 1H NMR, LC/MS and elemental analyses. Pre- liminary bioassay showed that most of title compounds had good herbicidal activity, for example, 4c-4f exhibited more than 90% inhibition to Abutilon theophrasti Medic, Amaranthus spinosus, Chenopodium album, Digitaria sanguinalis, Echinochloa crus-galli, and Setaria viridis at active ingredient 75 g a.i./hm2 in post-emergence treatment.
Key concepts: Abutilon, Trifluoromethyl, Digitaria sanguinalis, Echinochloa, Urea, Setaria viridis, Chemistry, Bioassay