NZ213401A - Sulphamoyl urea derivatives and herbicidal compositions - Google Patents
Sulphamoyl urea derivatives and herbicidal compositionsInfo
- Publication number
- NZ213401A NZ213401A NZ21340185A NZ21340185A NZ213401A NZ 213401 A NZ213401 A NZ 213401A NZ 21340185 A NZ21340185 A NZ 21340185A NZ 21340185 A NZ21340185 A NZ 21340185A NZ 213401 A NZ213401 A NZ 213401A
- Authority
- NZ
- New Zealand
- Prior art keywords
- compound
- alkyl
- hydrogen
- weeds
- mixture
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims description 27
- 230000002363 herbicidal effect Effects 0.000 title claims description 6
- OJXASOYYODXRPT-UHFFFAOYSA-N sulfamoylurea Chemical class NC(=O)NS(N)(=O)=O OJXASOYYODXRPT-UHFFFAOYSA-N 0.000 title description 4
- 150000001875 compounds Chemical class 0.000 claims description 35
- 241000196324 Embryophyta Species 0.000 claims description 24
- 125000000217 alkyl group Chemical group 0.000 claims description 12
- 238000009472 formulation Methods 0.000 claims description 11
- 239000001257 hydrogen Substances 0.000 claims description 9
- 229910052739 hydrogen Inorganic materials 0.000 claims description 9
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 8
- 239000004202 carbamide Substances 0.000 claims description 7
- 239000004009 herbicide Substances 0.000 claims description 7
- 238000000034 method Methods 0.000 claims description 7
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 5
- 229910052736 halogen Inorganic materials 0.000 claims description 5
- 150000002367 halogens Chemical class 0.000 claims description 5
- 244000058871 Echinochloa crus-galli Species 0.000 claims description 4
- 235000007320 Avena fatua Nutrition 0.000 claims description 3
- 244000075850 Avena orientalis Species 0.000 claims description 3
- 235000003403 Limnocharis flava Nutrition 0.000 claims description 3
- 235000005373 Uvularia sessilifolia Nutrition 0.000 claims description 3
- 125000003342 alkenyl group Chemical group 0.000 claims description 2
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims description 2
- 125000003545 alkoxy group Chemical group 0.000 claims description 2
- 125000000304 alkynyl group Chemical group 0.000 claims description 2
- 125000001188 haloalkyl group Chemical group 0.000 claims description 2
- 150000002431 hydrogen Chemical class 0.000 claims description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
- 239000001963 growth medium Substances 0.000 claims 2
- 244000278243 Limnocharis flava Species 0.000 claims 1
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 21
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 12
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 9
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 7
- 239000002904 solvent Substances 0.000 description 7
- 239000000243 solution Substances 0.000 description 6
- 239000002689 soil Substances 0.000 description 5
- 239000007787 solid Substances 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- 240000008100 Brassica rapa Species 0.000 description 4
- 238000005481 NMR spectroscopy Methods 0.000 description 4
- 230000006378 damage Effects 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- 229910000029 sodium carbonate Inorganic materials 0.000 description 4
- 235000011292 Brassica rapa Nutrition 0.000 description 3
- 235000004977 Brassica sinapistrum Nutrition 0.000 description 3
- 235000005853 Cyperus esculentus Nutrition 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 3
- 240000002439 Sorghum halepense Species 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 150000001412 amines Chemical class 0.000 description 3
- 239000000969 carrier Substances 0.000 description 3
- -1 dlatomaceous earth Substances 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- FIDRAVVQGKNYQK-UHFFFAOYSA-N 1,2,3,4-tetrahydrotriazine Chemical compound C1NNNC=C1 FIDRAVVQGKNYQK-UHFFFAOYSA-N 0.000 description 2
- 240000000321 Abutilon grandifolium Species 0.000 description 2
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
- 240000006122 Chenopodium album Species 0.000 description 2
- 235000009344 Chenopodium album Nutrition 0.000 description 2
- 235000007542 Cichorium intybus Nutrition 0.000 description 2
- 244000298479 Cichorium intybus Species 0.000 description 2
- 240000001505 Cyperus odoratus Species 0.000 description 2
- 240000008853 Datura stramonium Species 0.000 description 2
- 235000010823 Digitaria sanguinalis Nutrition 0.000 description 2
- 244000025670 Eleusine indica Species 0.000 description 2
- 235000014716 Eleusine indica Nutrition 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 2
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
- 240000003194 Sida rhombifolia Species 0.000 description 2
- 235000002834 Sida rhombifolia Nutrition 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 208000027418 Wounds and injury Diseases 0.000 description 2
- 239000002671 adjuvant Substances 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- WRJWRGBVPUUDLA-UHFFFAOYSA-N chlorosulfonyl isocyanate Chemical compound ClS(=O)(=O)N=C=O WRJWRGBVPUUDLA-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 230000008020 evaporation Effects 0.000 description 2
- 239000008187 granular material Substances 0.000 description 2
- 238000004128 high performance liquid chromatography Methods 0.000 description 2
- 208000014674 injury Diseases 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 239000012044 organic layer Substances 0.000 description 2
- 239000012074 organic phase Substances 0.000 description 2
- 235000011837 pasties Nutrition 0.000 description 2
- 238000005191 phase separation Methods 0.000 description 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 239000012258 stirred mixture Substances 0.000 description 2
- PYOKUURKVVELLB-UHFFFAOYSA-N trimethyl orthoformate Chemical compound COC(OC)OC PYOKUURKVVELLB-UHFFFAOYSA-N 0.000 description 2
- BBWLVVPHYQCHBZ-UHFFFAOYSA-N 2-(1,3-dioxolan-2-ylmethyl)aniline Chemical compound NC1=CC=CC=C1CC1OCCO1 BBWLVVPHYQCHBZ-UHFFFAOYSA-N 0.000 description 1
- JTWHVBNYYWFXSI-UHFFFAOYSA-N 2-nitro-1-phenylethanone Chemical compound [O-][N+](=O)CC(=O)C1=CC=CC=C1 JTWHVBNYYWFXSI-UHFFFAOYSA-N 0.000 description 1
- OOHIAOSLOGDBCE-UHFFFAOYSA-N 6-chloro-4-n-cyclopropyl-2-n-propan-2-yl-1,3,5-triazine-2,4-diamine Chemical compound CC(C)NC1=NC(Cl)=NC(NC2CC2)=N1 OOHIAOSLOGDBCE-UHFFFAOYSA-N 0.000 description 1
- 241000132076 Acroptilon Species 0.000 description 1
- 240000001592 Amaranthus caudatus Species 0.000 description 1
- 235000009328 Amaranthus caudatus Nutrition 0.000 description 1
- 235000013479 Amaranthus retroflexus Nutrition 0.000 description 1
- 235000004135 Amaranthus viridis Nutrition 0.000 description 1
- 244000036975 Ambrosia artemisiifolia Species 0.000 description 1
- 235000003129 Ambrosia artemisiifolia var elatior Nutrition 0.000 description 1
- 240000005528 Arctium lappa Species 0.000 description 1
- 235000003130 Arctium lappa Nutrition 0.000 description 1
- 235000008078 Arctium minus Nutrition 0.000 description 1
- 235000005637 Brassica campestris Nutrition 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- 241001148727 Bromus tectorum Species 0.000 description 1
- BMTAFVWTTFSTOG-UHFFFAOYSA-N Butylate Chemical compound CCSC(=O)N(CC(C)C)CC(C)C BMTAFVWTTFSTOG-UHFFFAOYSA-N 0.000 description 1
- 235000010301 Carolina horsenettle Nutrition 0.000 description 1
- 241000132585 Centaurea calcitrapa Species 0.000 description 1
- 235000005484 Chenopodium berlandieri Nutrition 0.000 description 1
- 235000009332 Chenopodium rubrum Nutrition 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 235000005918 Cirsium arvense Nutrition 0.000 description 1
- 240000001579 Cirsium arvense Species 0.000 description 1
- 244000272323 Cirsium lanceolatum Species 0.000 description 1
- 235000010856 Cirsium lanceolatum Nutrition 0.000 description 1
- 244000075634 Cyperus rotundus Species 0.000 description 1
- 235000001602 Digitaria X umfolozi Nutrition 0.000 description 1
- 235000017898 Digitaria ciliaris Nutrition 0.000 description 1
- 235000005476 Digitaria cruciata Nutrition 0.000 description 1
- 235000006830 Digitaria didactyla Nutrition 0.000 description 1
- 235000005804 Digitaria eriantha ssp. eriantha Nutrition 0.000 description 1
- 244000152970 Digitaria sanguinalis Species 0.000 description 1
- GUVLYNGULCJVDO-UHFFFAOYSA-N EPTC Chemical compound CCCN(CCC)C(=O)SCC GUVLYNGULCJVDO-UHFFFAOYSA-N 0.000 description 1
- 241000508725 Elymus repens Species 0.000 description 1
- 241000195955 Equisetum hyemale Species 0.000 description 1
- 241000490229 Eucephalus Species 0.000 description 1
- 244000207543 Euphorbia heterophylla Species 0.000 description 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- 235000014820 Galium aparine Nutrition 0.000 description 1
- 241000169130 Heteranthera limosa Species 0.000 description 1
- 235000017335 Hordeum vulgare subsp spontaneum Nutrition 0.000 description 1
- 241001299819 Hordeum vulgare subsp. spontaneum Species 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 206010061217 Infestation Diseases 0.000 description 1
- 240000001549 Ipomoea eriocarpa Species 0.000 description 1
- 235000005146 Ipomoea eriocarpa Nutrition 0.000 description 1
- 241000209082 Lolium Species 0.000 description 1
- 241000083473 Lychnis Species 0.000 description 1
- 235000000060 Malva neglecta Nutrition 0.000 description 1
- 240000000982 Malva neglecta Species 0.000 description 1
- 235000012629 Mentha aquatica Nutrition 0.000 description 1
- 235000009382 Mollugo verticillata Nutrition 0.000 description 1
- 235000015225 Panicum colonum Nutrition 0.000 description 1
- 240000000275 Persicaria hydropiper Species 0.000 description 1
- 235000017337 Persicaria hydropiper Nutrition 0.000 description 1
- 240000005218 Phyla nodiflora Species 0.000 description 1
- 241000209504 Poaceae Species 0.000 description 1
- 244000292697 Polygonum aviculare Species 0.000 description 1
- 235000006386 Polygonum aviculare Nutrition 0.000 description 1
- 235000004442 Polygonum persicaria Nutrition 0.000 description 1
- 244000234609 Portulaca oleracea Species 0.000 description 1
- 235000001855 Portulaca oleracea Nutrition 0.000 description 1
- 241000756999 Potamogetonaceae Species 0.000 description 1
- 235000015422 Rumex crispus ssp. crispus Nutrition 0.000 description 1
- 235000015426 Rumex crispus ssp. fauriei Nutrition 0.000 description 1
- 244000207667 Rumex vesicarius Species 0.000 description 1
- 235000008515 Setaria glauca Nutrition 0.000 description 1
- 235000001155 Setaria leucopila Nutrition 0.000 description 1
- 244000010062 Setaria pumila Species 0.000 description 1
- 241000501039 Solanum carolinense Species 0.000 description 1
- 240000001949 Taraxacum officinale Species 0.000 description 1
- 235000005187 Taraxacum officinale ssp. officinale Nutrition 0.000 description 1
- 235000008214 Thlaspi arvense Nutrition 0.000 description 1
- 240000008488 Thlaspi arvense Species 0.000 description 1
- 240000000260 Typha latifolia Species 0.000 description 1
- 241000159750 Urtica cannabina Species 0.000 description 1
- 235000013018 Vernonia anthelmintica Nutrition 0.000 description 1
- 244000145469 Vernonia anthelmintica Species 0.000 description 1
- 244000067505 Xanthium strumarium Species 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- NUFNQYOELLVIPL-UHFFFAOYSA-N acifluorfen Chemical compound C1=C([N+]([O-])=O)C(C(=O)O)=CC(OC=2C(=CC(=CC=2)C(F)(F)F)Cl)=C1 NUFNQYOELLVIPL-UHFFFAOYSA-N 0.000 description 1
- XCSGPAVHZFQHGE-UHFFFAOYSA-N alachlor Chemical compound CCC1=CC=CC(CC)=C1N(COC)C(=O)CCl XCSGPAVHZFQHGE-UHFFFAOYSA-N 0.000 description 1
- RQVYBGPQFYCBGX-UHFFFAOYSA-N ametryn Chemical compound CCNC1=NC(NC(C)C)=NC(SC)=N1 RQVYBGPQFYCBGX-UHFFFAOYSA-N 0.000 description 1
- 235000003484 annual ragweed Nutrition 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- ZOMSMJKLGFBRBS-UHFFFAOYSA-N bentazone Chemical compound C1=CC=C2NS(=O)(=O)N(C(C)C)C(=O)C2=C1 ZOMSMJKLGFBRBS-UHFFFAOYSA-N 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 235000010310 bull nettle Nutrition 0.000 description 1
- 235000006263 bur ragweed Nutrition 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 235000003488 common ragweed Nutrition 0.000 description 1
- 235000010313 devils tomato Nutrition 0.000 description 1
- 229960004132 diethyl ether Drugs 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000004495 emulsifiable concentrate Substances 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 230000009969 flowable effect Effects 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 230000012010 growth Effects 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- 238000002386 leaching Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000001473 noxious effect Effects 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- ISEUFVQQFVOBCY-UHFFFAOYSA-N prometon Chemical compound COC1=NC(NC(C)C)=NC(NC(C)C)=N1 ISEUFVQQFVOBCY-UHFFFAOYSA-N 0.000 description 1
- AAEVYOVXGOFMJO-UHFFFAOYSA-N prometryn Chemical compound CSC1=NC(NC(C)C)=NC(NC(C)C)=N1 AAEVYOVXGOFMJO-UHFFFAOYSA-N 0.000 description 1
- VXPLXMJHHKHSOA-UHFFFAOYSA-N propham Chemical compound CC(C)OC(=O)NC1=CC=CC=C1 VXPLXMJHHKHSOA-UHFFFAOYSA-N 0.000 description 1
- 238000010926 purge Methods 0.000 description 1
- 235000009736 ragweed Nutrition 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- ODCWYMIRDDJXKW-UHFFFAOYSA-N simazine Chemical compound CCNC1=NC(Cl)=NC(NCC)=N1 ODCWYMIRDDJXKW-UHFFFAOYSA-N 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000012265 solid product Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000000967 suction filtration Methods 0.000 description 1
- 239000000375 suspending agent Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- IROINLKCQGIITA-UHFFFAOYSA-N terbutryn Chemical compound CCNC1=NC(NC(C)(C)C)=NC(SC)=N1 IROINLKCQGIITA-UHFFFAOYSA-N 0.000 description 1
- 150000003558 thiocarbamic acid derivatives Chemical class 0.000 description 1
- 238000003971 tillage Methods 0.000 description 1
- 238000001291 vacuum drying Methods 0.000 description 1
- 230000009105 vegetative growth Effects 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
Landscapes
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US06/677,617 US4559081A (en) | 1984-12-03 | 1984-12-03 | Sulfamoyl urea derivatives |
US06/698,001 US4592776A (en) | 1985-02-04 | 1985-02-04 | Sulfamoyl urea derivatives |
Publications (1)
Publication Number | Publication Date |
---|---|
NZ213401A true NZ213401A (en) | 1987-11-27 |
Family
ID=27101842
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NZ21340185A NZ213401A (en) | 1984-12-03 | 1985-09-09 | Sulphamoyl urea derivatives and herbicidal compositions |
Country Status (8)
Country | Link |
---|---|
AR (1) | AR241135A1 (es) |
AU (1) | AU559017B2 (es) |
CA (1) | CA1229608A (es) |
DE (1) | DE3583491D1 (es) |
HU (1) | HU197173B (es) |
NZ (1) | NZ213401A (es) |
PL (1) | PL148736B1 (es) |
SU (1) | SU1517750A3 (es) |
-
1985
- 1985-09-09 NZ NZ21340185A patent/NZ213401A/en unknown
- 1985-09-19 AU AU47618/85A patent/AU559017B2/en not_active Ceased
- 1985-11-04 CA CA000494537A patent/CA1229608A/en not_active Expired
- 1985-11-22 AR AR30234785A patent/AR241135A1/es active
- 1985-11-26 PL PL25645285A patent/PL148736B1/pl unknown
- 1985-11-27 DE DE8585115026T patent/DE3583491D1/de not_active Expired - Lifetime
- 1985-12-02 SU SU853987358A patent/SU1517750A3/ru active
- 1985-12-02 HU HU460185A patent/HU197173B/hu not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
AU559017B2 (en) | 1987-02-19 |
AR241135A2 (es) | 1991-11-29 |
DE3583491D1 (de) | 1991-08-22 |
HU197173B (en) | 1989-03-28 |
HUT39332A (en) | 1986-09-29 |
PL148736B1 (en) | 1989-11-30 |
PL256452A1 (en) | 1987-10-05 |
SU1517750A3 (ru) | 1989-10-23 |
AU4761885A (en) | 1986-06-12 |
AR241135A1 (es) | 1991-11-29 |
CA1229608A (en) | 1987-11-24 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US4559081A (en) | Sulfamoyl urea derivatives | |
US4622065A (en) | Sulfamoyl urea derivatives | |
AU605889B2 (en) | Herbicidally active arloxy saturated 5-membered benzo-fused-heterocyclic compounds | |
EP0193700B1 (en) | Herbicidally active substituted benzisoxazole (or benzisothiazone) compounds | |
CA1205077A (en) | Herbicidally active 3-isoxazolyl-2-imidazolidinone derivatives | |
US4571255A (en) | Subsituted phenoxybenzisoxazole herbicides | |
US4756744A (en) | Herbicidally active 4-aminoalkylamino-3-isoxazolyl-2-imidazolidinone derivatives | |
US4696695A (en) | Sulfamoyl urea derivatives | |
US4717414A (en) | Herbicidally active imidazopyrrolo-pyridine (or benzene) derivatives | |
EP0184122B1 (en) | Sulfamoyl urea derivatives | |
US4741762A (en) | Sulfamoyl urea derivatives | |
US4592776A (en) | Sulfamoyl urea derivatives | |
KR910004434B1 (ko) | 치환된 티오펜설폰아미드 화합물의 제조방법 | |
US4666508A (en) | Sulfamoyl urea derivatives | |
US4790868A (en) | Herbicidally active substituted phenoxy or phenylthio benzoxazolone (or benzthiazolone) compounds | |
US4602939A (en) | Sulfamoyl urea derivatives | |
US4596883A (en) | Herbicidally active substituted diphenyl ethers | |
NZ213401A (en) | Sulphamoyl urea derivatives and herbicidal compositions | |
US4707180A (en) | Herbicidally active isoxazolyl-imidazolidinone derivatives | |
US4657580A (en) | Herbicidally active substituted diphenyl ether oxime derivatives | |
US4746351A (en) | Herbicidally active substituted phenoxy benzoxazole (or benzothiazole) | |
CA1235702A (en) | 2-alkylcarbonylphenylsulfamoyl-triazinyl or pyrimidinyl ureas | |
EP0155613A2 (en) | Diphenylether oxime ester derivatives | |
US4836845A (en) | Herbicidally active isoxazolyl-imadazolidinone derivatives | |
US4501924A (en) | Herbicidally active substituted diphenyl ether acetals or ketals |