IE46502B1 - Imidazole derivatives having herbicidal activity - Google Patents

Info

Publication number

IE46502B1

IE46502B1 IE431/78A IE43178A IE46502B1 IE 46502 B1 IE46502 B1 IE 46502B1 IE 431/78 A IE431/78 A IE 431/78A IE 43178 A IE43178 A IE 43178A IE 46502 B1 IE46502 B1 IE 46502B1

Authority

IE

Ireland

Prior art keywords

imidazole

dicarboxamide

dimethyl

ethyl

spp

Prior art date

1977-03-04

Links

• Espacenet
• Global Dossier
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• 150000002460 imidazoles Chemical class 0.000 title claims abstract description 49
• 229940079865 intestinal antiinfectives imidazole derivative Drugs 0.000 title claims abstract description 21
• 230000002363 herbicidal effect Effects 0.000 title claims description 48
• 150000001875 compounds Chemical class 0.000 claims abstract description 88
• 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims abstract description 48
• 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 22
• 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims abstract description 13
• 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 12
• 239000001257 hydrogen Substances 0.000 claims abstract description 12
• 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims abstract description 12
• 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 11
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 11
• 125000000217 alkyl group Chemical group 0.000 claims abstract description 8
• 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims abstract description 8
• 125000005843 halogen group Chemical group 0.000 claims abstract description 7
• 239000004009 herbicide Substances 0.000 claims abstract description 7
• 125000001153 fluoro group Chemical group F* 0.000 claims abstract description 5
• 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 claims abstract description 5
• 125000003342 alkenyl group Chemical group 0.000 claims abstract description 3
• 125000000304 alkynyl group Chemical group 0.000 claims abstract description 3
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• 238000000034 method Methods 0.000 claims description 51
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• 238000006243 chemical reaction Methods 0.000 claims description 35
• 230000012010 growth Effects 0.000 claims description 35
• 238000002360 preparation method Methods 0.000 claims description 32
• BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 claims description 28
• -1 trifluoromethoxy, methyl Chemical group 0.000 claims description 20
• 239000003085 diluting agent Substances 0.000 claims description 18
• 239000011149 active material Substances 0.000 claims description 16
• RAXXELZNTBOGNW-UHFFFAOYSA-N 1H-imidazole Chemical compound C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 claims description 12
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