DE2217721A1 - Verfahren zur bekaempfung unerwuenschter pflanzen - Google Patents
Verfahren zur bekaempfung unerwuenschter pflanzenInfo
- Publication number
- DE2217721A1 DE2217721A1 DE2217721A DE2217721A DE2217721A1 DE 2217721 A1 DE2217721 A1 DE 2217721A1 DE 2217721 A DE2217721 A DE 2217721A DE 2217721 A DE2217721 A DE 2217721A DE 2217721 A1 DE2217721 A1 DE 2217721A1
- Authority
- DE
- Germany
- Prior art keywords
- radical
- compound
- lower alkyl
- active ingredient
- halogen
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 238000000034 method Methods 0.000 title description 12
- -1 alkyl radical Chemical class 0.000 claims description 27
- 150000001875 compounds Chemical class 0.000 claims description 15
- 229910052736 halogen Inorganic materials 0.000 claims description 6
- 244000045561 useful plants Species 0.000 claims description 6
- 125000004432 carbon atom Chemical group C* 0.000 claims description 5
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical class [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 claims description 4
- 150000002148 esters Chemical class 0.000 claims description 3
- 125000005843 halogen group Chemical group 0.000 claims description 3
- SLRMQYXOBQWXCR-UHFFFAOYSA-N 2154-56-5 Chemical compound [CH2]C1=CC=CC=C1 SLRMQYXOBQWXCR-UHFFFAOYSA-N 0.000 claims description 2
- WZKSXHQDXQKIQJ-UHFFFAOYSA-N F[C](F)F Chemical compound F[C](F)F WZKSXHQDXQKIQJ-UHFFFAOYSA-N 0.000 claims description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- 239000002253 acid Substances 0.000 claims description 2
- RMRFFCXPLWYOOY-UHFFFAOYSA-N allyl radical Chemical class [CH2]C=C RMRFFCXPLWYOOY-UHFFFAOYSA-N 0.000 claims description 2
- ARUKYTASOALXFG-UHFFFAOYSA-N cycloheptylcycloheptane Chemical group C1CCCCCC1C1CCCCCC1 ARUKYTASOALXFG-UHFFFAOYSA-N 0.000 claims description 2
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- 125000000896 monocarboxylic acid group Chemical group 0.000 claims description 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 2
- 150000003254 radicals Chemical class 0.000 claims 3
- 239000004480 active ingredient Substances 0.000 description 72
- 241000196324 Embryophyta Species 0.000 description 29
- 238000009331 sowing Methods 0.000 description 13
- 244000024671 Brassica kaber Species 0.000 description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- 235000008427 Brassica arvensis Nutrition 0.000 description 9
- 235000004977 Brassica sinapistrum Nutrition 0.000 description 9
- 244000292693 Poa annua Species 0.000 description 9
- 244000285774 Cyperus esculentus Species 0.000 description 5
- 235000005853 Cyperus esculentus Nutrition 0.000 description 5
- 240000007594 Oryza sativa Species 0.000 description 5
- 235000007164 Oryza sativa Nutrition 0.000 description 5
- 239000002689 soil Substances 0.000 description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- 244000058871 Echinochloa crus-galli Species 0.000 description 4
- 235000010469 Glycine max Nutrition 0.000 description 4
- 235000011999 Panicum crusgalli Nutrition 0.000 description 4
- 244000062793 Sorghum vulgare Species 0.000 description 4
- 241001506766 Xanthium Species 0.000 description 4
- 240000008042 Zea mays Species 0.000 description 4
- 239000013543 active substance Substances 0.000 description 4
- 235000019713 millet Nutrition 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- ZFXYFBGIUFBOJW-UHFFFAOYSA-N theophylline Chemical compound O=C1N(C)C(=O)N(C)C2=C1NC=N2 ZFXYFBGIUFBOJW-UHFFFAOYSA-N 0.000 description 4
- 229960000278 theophylline Drugs 0.000 description 4
- 244000291564 Allium cepa Species 0.000 description 3
- 241001621841 Alopecurus myosuroides Species 0.000 description 3
- 240000001592 Amaranthus caudatus Species 0.000 description 3
- 235000009328 Amaranthus caudatus Nutrition 0.000 description 3
- 240000005528 Arctium lappa Species 0.000 description 3
- 235000003130 Arctium lappa Nutrition 0.000 description 3
- 235000008078 Arctium minus Nutrition 0.000 description 3
- 235000005637 Brassica campestris Nutrition 0.000 description 3
- 235000014750 Brassica kaber Nutrition 0.000 description 3
- 235000010149 Brassica rapa subsp chinensis Nutrition 0.000 description 3
- 235000010570 Brassica rapa var. rapa Nutrition 0.000 description 3
- 244000025254 Cannabis sativa Species 0.000 description 3
- 241000234653 Cyperus Species 0.000 description 3
- 235000014820 Galium aparine Nutrition 0.000 description 3
- 240000005702 Galium aparine Species 0.000 description 3
- 241000287828 Gallus gallus Species 0.000 description 3
- 244000042664 Matricaria chamomilla Species 0.000 description 3
- 235000007232 Matricaria chamomilla Nutrition 0.000 description 3
- 235000002595 Solanum tuberosum Nutrition 0.000 description 3
- 244000061456 Solanum tuberosum Species 0.000 description 3
- 240000006694 Stellaria media Species 0.000 description 3
- 244000098338 Triticum aestivum Species 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- CWOBGOXHYZMVNY-UHFFFAOYSA-N methyl 2,3,5,6-tetrachloro-4-[methoxy(methyl)carbamoyl]benzoate Chemical compound CON(C)C(=O)C1=C(Cl)C(Cl)=C(C(=O)OC)C(Cl)=C1Cl CWOBGOXHYZMVNY-UHFFFAOYSA-N 0.000 description 3
- XITQUSLLOSKDTB-UHFFFAOYSA-N nitrofen Chemical compound C1=CC([N+](=O)[O-])=CC=C1OC1=CC=C(Cl)C=C1Cl XITQUSLLOSKDTB-UHFFFAOYSA-N 0.000 description 3
- ASRSBXRMOCLKQC-UHFFFAOYSA-N 2-(4-chloro-2-methylphenoxy)-n-methoxyacetamide Chemical compound CONC(=O)COC1=CC=C(Cl)C=C1C ASRSBXRMOCLKQC-UHFFFAOYSA-N 0.000 description 2
- UOQJYFBKWJMHIQ-UHFFFAOYSA-N 3-methyl-6-(2-methylphenyl)sulfanylpyridazine Chemical compound N1=NC(C)=CC=C1SC1=CC=CC=C1C UOQJYFBKWJMHIQ-UHFFFAOYSA-N 0.000 description 2
- 235000013291 Alisma plantago aquatica Nutrition 0.000 description 2
- 240000004615 Alisma plantago-aquatica Species 0.000 description 2
- 235000005255 Allium cepa Nutrition 0.000 description 2
- 241000743985 Alopecurus Species 0.000 description 2
- 235000007320 Avena fatua Nutrition 0.000 description 2
- 241000209764 Avena fatua Species 0.000 description 2
- 244000152970 Digitaria sanguinalis Species 0.000 description 2
- 235000010823 Digitaria sanguinalis Nutrition 0.000 description 2
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 2
- 241000192043 Echinochloa Species 0.000 description 2
- 240000005979 Hordeum vulgare Species 0.000 description 2
- 235000007340 Hordeum vulgare Nutrition 0.000 description 2
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical class [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 244000286177 Raphanus raphanistrum Species 0.000 description 2
- 244000067505 Xanthium strumarium Species 0.000 description 2
- 235000007244 Zea mays Nutrition 0.000 description 2
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical class OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000008187 granular material Substances 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 235000012015 potatoes Nutrition 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- VXPLXMJHHKHSOA-UHFFFAOYSA-N propham Chemical compound CC(C)OC(=O)NC1=CC=CC=C1 VXPLXMJHHKHSOA-UHFFFAOYSA-N 0.000 description 2
- PBMFSQRYOILNGV-UHFFFAOYSA-N pyridazine Chemical compound C1=CC=NN=C1 PBMFSQRYOILNGV-UHFFFAOYSA-N 0.000 description 2
- 235000009566 rice Nutrition 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- DSVOTYIOPGIVPP-UHFFFAOYSA-N (3,4-dichlorophenyl)methyl n-methylcarbamate Chemical compound CNC(=O)OCC1=CC=C(Cl)C(Cl)=C1 DSVOTYIOPGIVPP-UHFFFAOYSA-N 0.000 description 1
- CDPIAMPYDNIIHI-UHFFFAOYSA-N 2-phenoxy-1h-pyridazine Chemical compound N1C=CC=CN1OC1=CC=CC=C1 CDPIAMPYDNIIHI-UHFFFAOYSA-N 0.000 description 1
- REEXLQXWNOSJKO-UHFFFAOYSA-N 2h-1$l^{4},2,3-benzothiadiazine 1-oxide Chemical class C1=CC=C2S(=O)NN=CC2=C1 REEXLQXWNOSJKO-UHFFFAOYSA-N 0.000 description 1
- VQBQXLPOBZZZLL-UHFFFAOYSA-N 3-(2,4-dichlorophenyl)sulfanylpyridazine Chemical compound ClC1=CC(Cl)=CC=C1SC1=CC=CN=N1 VQBQXLPOBZZZLL-UHFFFAOYSA-N 0.000 description 1
- XEAYEFPRHATNAC-UHFFFAOYSA-N 3-(2,4-dimethylphenyl)sulfanyl-6-methylpyridazine Chemical compound CC1=CC(C)=CC=C1SC1=CC=C(C)N=N1 XEAYEFPRHATNAC-UHFFFAOYSA-N 0.000 description 1
- SCIKACPNLRPELG-UHFFFAOYSA-N 3-(2,5-dimethylphenoxy)pyridazine Chemical compound CC1=CC=C(C)C(OC=2N=NC=CC=2)=C1 SCIKACPNLRPELG-UHFFFAOYSA-N 0.000 description 1
- QIMHOOCLDKBEES-UHFFFAOYSA-N 3-(2-butan-2-yl-5-methylphenoxy)pyridazine Chemical compound CCC(C)C1=CC=C(C)C=C1OC1=CC=CN=N1 QIMHOOCLDKBEES-UHFFFAOYSA-N 0.000 description 1
- YXKARCIPERIRAB-UHFFFAOYSA-N 3-(2-butan-2-ylphenoxy)pyridazine Chemical compound CCC(C)C1=CC=CC=C1OC1=CC=CN=N1 YXKARCIPERIRAB-UHFFFAOYSA-N 0.000 description 1
- REBOCHOVNYUILK-UHFFFAOYSA-N 3-(2-ethylphenoxy)pyridazine Chemical compound CCC1=CC=CC=C1OC1=CC=CN=N1 REBOCHOVNYUILK-UHFFFAOYSA-N 0.000 description 1
- DWMXUXUDAWNDHA-UHFFFAOYSA-N 3-(2-propan-2-ylphenoxy)pyridazine Chemical compound CC(C)C1=CC=CC=C1OC1=CC=CN=N1 DWMXUXUDAWNDHA-UHFFFAOYSA-N 0.000 description 1
- ZCCWLVYDLOYYET-UHFFFAOYSA-N 3-(2-tert-butylphenoxy)pyridazine Chemical compound CC(C)(C)C1=CC=CC=C1OC1=CC=CN=N1 ZCCWLVYDLOYYET-UHFFFAOYSA-N 0.000 description 1
- OWKQMKRSKCMYRF-UHFFFAOYSA-N 3-(5-methyl-2-propan-2-ylphenoxy)pyridazine Chemical compound CC(C)C1=CC=C(C)C=C1OC1=CC=CN=N1 OWKQMKRSKCMYRF-UHFFFAOYSA-N 0.000 description 1
- FTXJUKILOHPHHB-UHFFFAOYSA-N 3-phenoxypyridazine Chemical compound C=1C=CN=NC=1OC1=CC=CC=C1 FTXJUKILOHPHHB-UHFFFAOYSA-N 0.000 description 1
- 125000006283 4-chlorobenzyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1Cl)C([H])([H])* 0.000 description 1
- 235000016626 Agrimonia eupatoria Nutrition 0.000 description 1
- 241000748223 Alisma Species 0.000 description 1
- 235000017300 Alisma plantago Nutrition 0.000 description 1
- 244000233890 Alisma plantago Species 0.000 description 1
- MDBGGTQNNUOQRC-UHFFFAOYSA-N Allidochlor Chemical compound ClCC(=O)N(CC=C)CC=C MDBGGTQNNUOQRC-UHFFFAOYSA-N 0.000 description 1
- 235000002732 Allium cepa var. cepa Nutrition 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- 244000105624 Arachis hypogaea Species 0.000 description 1
- 239000005711 Benzoic acid Chemical class 0.000 description 1
- 241000219198 Brassica Species 0.000 description 1
- 235000003351 Brassica cretica Nutrition 0.000 description 1
- 235000003343 Brassica rupestris Nutrition 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical class [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 235000007866 Chamaemelum nobile Nutrition 0.000 description 1
- HSSBORCLYSCBJR-UHFFFAOYSA-N Chloramben Chemical compound NC1=CC(Cl)=CC(C(O)=O)=C1Cl HSSBORCLYSCBJR-UHFFFAOYSA-N 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- 241000234646 Cyperaceae Species 0.000 description 1
- 235000017896 Digitaria Nutrition 0.000 description 1
- 241001303487 Digitaria <clam> Species 0.000 description 1
- QAHFOPIILNICLA-UHFFFAOYSA-N Diphenamid Chemical compound C=1C=CC=CC=1C(C(=O)N(C)C)C1=CC=CC=C1 QAHFOPIILNICLA-UHFFFAOYSA-N 0.000 description 1
- HHMCAJWVGYGUEF-UHFFFAOYSA-N Fluorodifen Chemical compound C1=CC([N+](=O)[O-])=CC=C1OC1=CC=C(C(F)(F)F)C=C1[N+]([O-])=O HHMCAJWVGYGUEF-UHFFFAOYSA-N 0.000 description 1
- 241000748465 Galinsoga Species 0.000 description 1
- 235000018914 Galinsoga parviflora Nutrition 0.000 description 1
- 244000214240 Galinsoga parviflora Species 0.000 description 1
- 244000068988 Glycine max Species 0.000 description 1
- 241000219146 Gossypium Species 0.000 description 1
- 241000209219 Hordeum Species 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical class 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
- 241000209510 Liliopsida Species 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical class [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- 235000017945 Matricaria Nutrition 0.000 description 1
- 240000004658 Medicago sativa Species 0.000 description 1
- 235000017587 Medicago sativa ssp. sativa Nutrition 0.000 description 1
- BAVYZALUXZFZLV-UHFFFAOYSA-O Methylammonium ion Chemical class [NH3+]C BAVYZALUXZFZLV-UHFFFAOYSA-O 0.000 description 1
- WXZVAROIGSFCFJ-UHFFFAOYSA-N N,N-diethyl-2-(naphthalen-1-yloxy)propanamide Chemical compound C1=CC=C2C(OC(C)C(=O)N(CC)CC)=CC=CC2=C1 WXZVAROIGSFCFJ-UHFFFAOYSA-N 0.000 description 1
- UEEJHVSXFDXPFK-UHFFFAOYSA-N N-dimethylaminoethanol Chemical compound CN(C)CCO UEEJHVSXFDXPFK-UHFFFAOYSA-N 0.000 description 1
- 241000282376 Panthera tigris Species 0.000 description 1
- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 1
- 244000046052 Phaseolus vulgaris Species 0.000 description 1
- 235000010582 Pisum sativum Nutrition 0.000 description 1
- 240000004713 Pisum sativum Species 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical class [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 241000220259 Raphanus Species 0.000 description 1
- 235000000241 Raphanus raphanistrum Nutrition 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 241000220261 Sinapis Species 0.000 description 1
- 240000007641 Spergula rubra Species 0.000 description 1
- 241000219793 Trifolium Species 0.000 description 1
- 235000021307 Triticum Nutrition 0.000 description 1
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
- 235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 description 1
- PXAJQJMDEXJWFB-UHFFFAOYSA-N acetone oxime Chemical compound CC(C)=NO PXAJQJMDEXJWFB-UHFFFAOYSA-N 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 125000005210 alkyl ammonium group Chemical group 0.000 description 1
- 125000003368 amide group Chemical group 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- VGPYEHKOIGNJKV-UHFFFAOYSA-N asulam Chemical compound COC(=O)NS(=O)(=O)C1=CC=C(N)C=C1 VGPYEHKOIGNJKV-UHFFFAOYSA-N 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- QKSKPIVNLNLAAV-UHFFFAOYSA-N bis(2-chloroethyl) sulfide Chemical compound ClCCSCCCl QKSKPIVNLNLAAV-UHFFFAOYSA-N 0.000 description 1
- 239000008280 blood Substances 0.000 description 1
- 210000004369 blood Anatomy 0.000 description 1
- 239000011575 calcium Chemical class 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 229940112021 centrally acting muscle relaxants carbamic acid ester Drugs 0.000 description 1
- 235000013339 cereals Nutrition 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 235000005822 corn Nutrition 0.000 description 1
- 229960002887 deanol Drugs 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012972 dimethylethanolamine Substances 0.000 description 1
- USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical class C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 125000001033 ether group Chemical group 0.000 description 1
- QUSNBJAOOMFDIB-UHFFFAOYSA-O ethylaminium Chemical class CC[NH3+] QUSNBJAOOMFDIB-UHFFFAOYSA-O 0.000 description 1
- 241001233957 eudicotyledons Species 0.000 description 1
- 239000003337 fertilizer Substances 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 230000002363 herbicidal effect Effects 0.000 description 1
- 239000004009 herbicide Substances 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- 150000002429 hydrazines Chemical class 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- BLNWTAHYTCHDJH-UHFFFAOYSA-O hydroxy(oxo)azanium Chemical compound O[NH+]=O BLNWTAHYTCHDJH-UHFFFAOYSA-O 0.000 description 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 125000000468 ketone group Chemical group 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 235000009973 maize Nutrition 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- UFEJKYYYVXYMMS-UHFFFAOYSA-N methylcarbamic acid Chemical compound CNC(O)=O UFEJKYYYVXYMMS-UHFFFAOYSA-N 0.000 description 1
- 235000010460 mustard Nutrition 0.000 description 1
- 150000002790 naphthalenes Chemical class 0.000 description 1
- 235000014571 nuts Nutrition 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 235000020232 peanut Nutrition 0.000 description 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
- HKOOXMFOFWEVGF-UHFFFAOYSA-N phenylhydrazine Chemical compound NNC1=CC=CC=C1 HKOOXMFOFWEVGF-UHFFFAOYSA-N 0.000 description 1
- 229940067157 phenylhydrazine Drugs 0.000 description 1
- 239000011591 potassium Chemical class 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- PHNUZKMIPFFYSO-UHFFFAOYSA-N propyzamide Chemical compound C#CC(C)(C)NC(=O)C1=CC(Cl)=CC(Cl)=C1 PHNUZKMIPFFYSO-UHFFFAOYSA-N 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 150000003503 terephthalic acid derivatives Chemical class 0.000 description 1
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 1
- 150000003560 thiocarbamic acids Chemical class 0.000 description 1
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical class CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N urethane group Chemical class NC(=O)OCC JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Priority Applications (30)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2217721A DE2217721A1 (de) | 1972-04-13 | 1972-04-13 | Verfahren zur bekaempfung unerwuenschter pflanzen |
| BG025070A BG20283A3 (bg) | 1972-04-13 | 1973-03-15 | Метод за борба с нежелана растителност |
| BG025069A BG20282A3 (bg) | 1972-04-13 | 1973-03-15 | Метод за борба с нежелана растителност |
| BG025066A BG20279A3 (bg) | 1972-04-13 | 1973-03-15 | Метод за борба с нежелана растителност |
| BG025071A BG20528A3 (bg) | 1972-04-13 | 1973-03-15 | Хербицидна смес |
| BG025068A BG20281A3 (bg) | 1972-04-13 | 1973-03-15 | Метод за борба с нежелана растителност |
| BG025064A BG20527A3 (bg) | 1972-04-13 | 1973-03-15 | Метод за борба с нежелана растителност |
| BG025712A BG20753A3 (bg) | 1972-04-13 | 1973-03-15 | Средство за борба с нежелана растителност |
| BG025065A BG20998A3 (bg) | 1972-04-13 | 1973-03-15 | Метод за борба с нежелана растителност |
| BG025067A BG20280A3 (bg) | 1972-04-13 | 1973-03-15 | Метод за борба с нежелана растителност |
| IL41819A IL41819A0 (en) | 1972-04-13 | 1973-03-19 | The control of the growth of unwanted plants by combined pre-and post-emergence treatment |
| AU53633/73A AU5363373A (en) | 1972-04-13 | 1973-03-22 | Control of unwanted plants |
| NL7304399A NL7304399A (enrdf_load_stackoverflow) | 1972-04-13 | 1973-03-29 | |
| DD169916A DD104013A5 (enrdf_load_stackoverflow) | 1972-04-13 | 1973-04-03 | |
| SU2040368A SU504448A3 (ru) | 1972-04-13 | 1973-04-05 | Гербицидный состав |
| SU2040369A SU496703A3 (ru) | 1972-04-13 | 1973-04-05 | Гербицидный состав |
| FR7312441A FR2179822B1 (enrdf_load_stackoverflow) | 1972-04-13 | 1973-04-06 | |
| ZA732443A ZA732443B (en) | 1972-04-13 | 1973-04-10 | Control of unwanted plants |
| OA54878A OA04529A (fr) | 1972-04-13 | 1973-04-11 | Lutte contre des plantes indésirables. |
| HUBA2910A HU166673B (enrdf_load_stackoverflow) | 1972-04-13 | 1973-04-11 | |
| IT49410/73A IT980187B (it) | 1972-04-13 | 1973-04-12 | Composizione erbicida per la lotta contro piante indesiderate |
| BE129940A BE798133A (fr) | 1972-04-13 | 1973-04-12 | Lutte contre des plantes indesirables |
| GB1719975A GB1420090A (en) | 1972-04-13 | 1973-04-12 | Herbicidal compositions |
| GB1755273A GB1420089A (en) | 1972-04-13 | 1973-04-12 | Control of unwanted plants |
| JP48040961A JPS497436A (enrdf_load_stackoverflow) | 1972-04-13 | 1973-04-12 | |
| BR732684A BR7302684D0 (pt) | 1972-04-13 | 1973-04-13 | Processo herbicida |
| DK672674A DK672674A (enrdf_load_stackoverflow) | 1972-04-13 | 1974-12-20 | |
| DK672574A DK672574A (enrdf_load_stackoverflow) | 1972-04-13 | 1974-12-20 | |
| DK672774A DK672774A (enrdf_load_stackoverflow) | 1972-04-13 | 1974-12-20 | |
| US05/551,129 US3963477A (en) | 1972-04-13 | 1975-02-19 | Herbicidal mixtures of S-halobenzyl-N,N-dialkylthiolcarbamates and 3-lower alkyl-2,1,3-benzothiadiazinone-(4)-2,2-dioxides and salts thereof |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2217721A DE2217721A1 (de) | 1972-04-13 | 1972-04-13 | Verfahren zur bekaempfung unerwuenschter pflanzen |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE2217721A1 true DE2217721A1 (de) | 1973-10-25 |
Family
ID=5841783
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE2217721A Pending DE2217721A1 (de) | 1972-04-13 | 1972-04-13 | Verfahren zur bekaempfung unerwuenschter pflanzen |
Country Status (16)
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR1480359A (fr) * | 1965-05-26 | 1967-05-12 | Sankyo Co | Nouvelles compositions herbicides à base de 3-phénoxypyridazines |
| FR1538698A (fr) * | 1966-08-30 | 1968-09-06 | Basf Ag | Agents herbicides |
| US3621017A (en) * | 1967-09-30 | 1971-11-16 | Basf Ag | Salts of thiadiazinones |
-
1972
- 1972-04-13 DE DE2217721A patent/DE2217721A1/de active Pending
-
1973
- 1973-03-15 BG BG025065A patent/BG20998A3/xx unknown
- 1973-03-15 BG BG025069A patent/BG20282A3/xx unknown
- 1973-03-15 BG BG025064A patent/BG20527A3/xx unknown
- 1973-03-15 BG BG025071A patent/BG20528A3/xx unknown
- 1973-03-15 BG BG025712A patent/BG20753A3/xx unknown
- 1973-03-15 BG BG025067A patent/BG20280A3/xx unknown
- 1973-03-15 BG BG025070A patent/BG20283A3/xx unknown
- 1973-03-15 BG BG025068A patent/BG20281A3/xx unknown
- 1973-03-15 BG BG025066A patent/BG20279A3/xx unknown
- 1973-03-19 IL IL41819A patent/IL41819A0/xx unknown
- 1973-03-22 AU AU53633/73A patent/AU5363373A/en not_active Expired
- 1973-03-29 NL NL7304399A patent/NL7304399A/xx unknown
- 1973-04-03 DD DD169916A patent/DD104013A5/xx unknown
- 1973-04-05 SU SU2040368A patent/SU504448A3/ru active
- 1973-04-05 SU SU2040369A patent/SU496703A3/ru active
- 1973-04-06 FR FR7312441A patent/FR2179822B1/fr not_active Expired
- 1973-04-10 ZA ZA732443A patent/ZA732443B/xx unknown
- 1973-04-11 HU HUBA2910A patent/HU166673B/hu unknown
- 1973-04-11 OA OA54878A patent/OA04529A/xx unknown
- 1973-04-12 GB GB1719975A patent/GB1420090A/en not_active Expired
- 1973-04-12 BE BE129940A patent/BE798133A/xx unknown
- 1973-04-12 JP JP48040961A patent/JPS497436A/ja active Pending
- 1973-04-12 IT IT49410/73A patent/IT980187B/it active
- 1973-04-12 GB GB1755273A patent/GB1420089A/en not_active Expired
- 1973-04-13 BR BR732684A patent/BR7302684D0/pt unknown
Also Published As
| Publication number | Publication date |
|---|---|
| GB1420090A (en) | 1976-01-07 |
| OA04529A (fr) | 1980-03-30 |
| ZA732443B (en) | 1974-02-27 |
| BR7302684D0 (pt) | 1974-08-15 |
| HU166673B (enrdf_load_stackoverflow) | 1975-05-28 |
| BG20281A3 (bg) | 1975-11-05 |
| JPS497436A (enrdf_load_stackoverflow) | 1974-01-23 |
| GB1420089A (en) | 1976-01-07 |
| BE798133A (fr) | 1973-10-12 |
| FR2179822A1 (enrdf_load_stackoverflow) | 1973-11-23 |
| NL7304399A (enrdf_load_stackoverflow) | 1973-10-16 |
| SU496703A3 (ru) | 1975-12-25 |
| SU504448A3 (ru) | 1976-02-25 |
| BG20282A3 (bg) | 1975-11-05 |
| BG20279A3 (bg) | 1975-11-05 |
| BG20753A3 (bg) | 1975-12-20 |
| IL41819A0 (en) | 1973-05-31 |
| IT980187B (it) | 1974-09-30 |
| BG20283A3 (bg) | 1975-11-05 |
| BG20527A3 (bg) | 1975-12-05 |
| DD104013A5 (enrdf_load_stackoverflow) | 1974-02-20 |
| FR2179822B1 (enrdf_load_stackoverflow) | 1976-06-11 |
| AU5363373A (en) | 1974-09-26 |
| BG20280A3 (bg) | 1975-11-05 |
| BG20528A3 (bg) | 1975-12-05 |
| BG20998A3 (bg) | 1976-01-20 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE2328340C3 (de) | N-aliphatoxyalkylierte Chloracetanilide, Verfahren zu deren Herstellung und Mittel zur Beeinflussung des Pflanzenwachstums | |
| DE3603789A1 (de) | N-substituierte 3,4,5,6-tetrahydrophthalimide | |
| DE2747531A1 (de) | Substituierte 3-aminopyrazole | |
| DE2639405A1 (de) | Neuer oximaether, verfahren zu dessen herstellung und seine verwendung als gegenmittel fuer kulturpflanzen schaedigende herbizide | |
| EP0003805B1 (de) | Pyridazonverbindungen und diese enthaltende herbizide Zusammensetzungen | |
| DE1542755A1 (de) | Verfahren zur Herstellung von Unkrautvernichtungsmitteln,diese enthaltende Mittel und deren Anwendung | |
| DE1189312B (de) | Mittel mit selektiver herbizider Wirkung | |
| DE1284151B (de) | Selektive herbicide Mittel | |
| EP0775124B1 (de) | Herbizide saccharincarbonsäure-derivate und verfahren zu ihrer herstellung | |
| DE2217722A1 (de) | Herbizid | |
| CH628017A5 (de) | Verfahren zur herstellung der neuen verbindung n-(4-benzyloxyphenyl)-n'-methyl-n'-methoxyharnstoff. | |
| EP0007089B1 (de) | Acylanilide mit herbicider und fungicider Wirkung, Verfahren zu ihrer Herstellung und ihre Verwendung | |
| DE2703838A1 (de) | Diurethane | |
| DE3047629A1 (de) | "tetrahydrofuranderivate" | |
| DE2217721A1 (de) | Verfahren zur bekaempfung unerwuenschter pflanzen | |
| DE1903198A1 (de) | Substituierte Anilide | |
| DE3300056C2 (de) | 3-Nitrobenzolsulfonanilid-Derivate und diese enthaltende fungizide Mittel | |
| WO1996005183A1 (de) | Saccharinderivate und ihre anwendung als herbizide | |
| CH403391A (de) | Herbicides Mittel, enthaltend neue Harnstoffe | |
| DD156413A5 (de) | Zusammensetzung mit wachstumsregulierung fuer pflanzen | |
| DE1300727B (de) | Verwendung von Dinitroanilinderivaten als selektive Vorauflaufherbizide | |
| EP0067381B1 (de) | Anilide, Verfahren zu ihrer Herstellung und diese enthaltende Herbizide | |
| DE2624094A1 (de) | N-carbamoyl-n-phenylaminosaeure-derivate, verfahren zu ihrer herstellung und herbizide mittel | |
| AT227020B (de) | Herbizide Mittel | |
| WO1996005179A1 (de) | Substituierte triazolinone als pflanzenschutzmittel |