ZA200208114B - Fungicidal combinations of active agents. - Google Patents
Fungicidal combinations of active agents. Download PDFInfo
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- ZA200208114B ZA200208114B ZA200208114A ZA200208114A ZA200208114B ZA 200208114 B ZA200208114 B ZA 200208114B ZA 200208114 A ZA200208114 A ZA 200208114A ZA 200208114 A ZA200208114 A ZA 200208114A ZA 200208114 B ZA200208114 B ZA 200208114B
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- South Africa
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- active compound
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- 230000000855 fungicidal effect Effects 0.000 title claims description 3
- 239000013543 active substance Substances 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims description 126
- 150000003852 triazoles Chemical class 0.000 claims description 17
- 229910052799 carbon Inorganic materials 0.000 claims description 12
- 239000000575 pesticide Substances 0.000 claims description 12
- 229910052739 hydrogen Inorganic materials 0.000 claims description 9
- 150000001448 anilines Chemical class 0.000 claims description 7
- 241000233866 Fungi Species 0.000 claims description 5
- WURBVZBTWMNKQT-UHFFFAOYSA-N 1-(4-chlorophenoxy)-3,3-dimethyl-1-(1,2,4-triazol-1-yl)butan-2-one Chemical compound C1=NC=NN1C(C(=O)C(C)(C)C)OC1=CC=C(Cl)C=C1 WURBVZBTWMNKQT-UHFFFAOYSA-N 0.000 claims description 4
- VGPIBGGRCVEHQZ-UHFFFAOYSA-N 1-(biphenyl-4-yloxy)-3,3-dimethyl-1-(1,2,4-triazol-1-yl)butan-2-ol Chemical compound C1=NC=NN1C(C(O)C(C)(C)C)OC(C=C1)=CC=C1C1=CC=CC=C1 VGPIBGGRCVEHQZ-UHFFFAOYSA-N 0.000 claims description 4
- MGNFYQILYYYUBS-UHFFFAOYSA-N 1-[3-(4-tert-butylphenyl)-2-methylpropyl]piperidine Chemical compound C=1C=C(C(C)(C)C)C=CC=1CC(C)CN1CCCCC1 MGNFYQILYYYUBS-UHFFFAOYSA-N 0.000 claims description 4
- IUOKJNROJISWRO-UHFFFAOYSA-N N-(2-cyano-3-methylbutan-2-yl)-2-(2,4-dichlorophenoxy)propanamide Chemical compound CC(C)C(C)(C#N)NC(=O)C(C)OC1=CC=C(Cl)C=C1Cl IUOKJNROJISWRO-UHFFFAOYSA-N 0.000 claims description 4
- CRQQGFGUEAVUIL-UHFFFAOYSA-N chlorothalonil Chemical compound ClC1=C(Cl)C(C#N)=C(Cl)C(C#N)=C1Cl CRQQGFGUEAVUIL-UHFFFAOYSA-N 0.000 claims description 4
- 239000000203 mixture Substances 0.000 claims description 4
- WRPIRSINYZBGPK-UHFFFAOYSA-N quinoxyfen Chemical compound C1=CC(F)=CC=C1OC1=CC=NC2=CC(Cl)=CC(Cl)=C12 WRPIRSINYZBGPK-UHFFFAOYSA-N 0.000 claims description 4
- BAZVSMNPJJMILC-UHFFFAOYSA-N triadimenol Chemical compound C1=NC=NN1C(C(O)C(C)(C)C)OC1=CC=C(Cl)C=C1 BAZVSMNPJJMILC-UHFFFAOYSA-N 0.000 claims description 4
- RYAUSSKQMZRMAI-ALOPSCKCSA-N (2S,6R)-4-[3-(4-tert-butylphenyl)-2-methylpropyl]-2,6-dimethylmorpholine Chemical compound C=1C=C(C(C)(C)C)C=CC=1CC(C)CN1C[C@H](C)O[C@H](C)C1 RYAUSSKQMZRMAI-ALOPSCKCSA-N 0.000 claims description 3
- 239000005846 Triadimenol Substances 0.000 claims description 3
- YWTYJOPNNQFBPC-UHFFFAOYSA-N imidacloprid Chemical compound [O-][N+](=O)\N=C1/NCCN1CC1=CC=C(Cl)N=C1 YWTYJOPNNQFBPC-UHFFFAOYSA-N 0.000 claims description 3
- 150000002460 imidazoles Chemical class 0.000 claims description 3
- ZMYFCFLJBGAQRS-IRXDYDNUSA-N (2R,3S)-epoxiconazole Chemical compound C1=CC(F)=CC=C1[C@@]1(CN2N=CN=C2)[C@H](C=2C(=CC=CC=2)Cl)O1 ZMYFCFLJBGAQRS-IRXDYDNUSA-N 0.000 claims description 2
- PXMNMQRDXWABCY-UHFFFAOYSA-N 1-(4-chlorophenyl)-4,4-dimethyl-3-(1H-1,2,4-triazol-1-ylmethyl)pentan-3-ol Chemical compound C1=NC=NN1CC(O)(C(C)(C)C)CCC1=CC=C(Cl)C=C1 PXMNMQRDXWABCY-UHFFFAOYSA-N 0.000 claims description 2
- WKBPZYKAUNRMKP-UHFFFAOYSA-N 1-[2-(2,4-dichlorophenyl)pentyl]1,2,4-triazole Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(CCC)CN1C=NC=N1 WKBPZYKAUNRMKP-UHFFFAOYSA-N 0.000 claims description 2
- UFNOUKDBUJZYDE-UHFFFAOYSA-N 2-(4-chlorophenyl)-3-cyclopropyl-1-(1H-1,2,4-triazol-1-yl)butan-2-ol Chemical compound C1=NC=NN1CC(O)(C=1C=CC(Cl)=CC=1)C(C)C1CC1 UFNOUKDBUJZYDE-UHFFFAOYSA-N 0.000 claims description 2
- CIIBXKOZNOARPC-UHFFFAOYSA-N 3-tert-butyl-n-ethyl-7-methyl-n-propyl-6,9-dioxaspiro[4.5]decan-7-amine Chemical compound O1C(N(CC)CCC)(C)COCC11CC(C(C)(C)C)CC1 CIIBXKOZNOARPC-UHFFFAOYSA-N 0.000 claims description 2
- 239000005730 Azoxystrobin Substances 0.000 claims description 2
- 239000005747 Chlorothalonil Substances 0.000 claims description 2
- 239000005757 Cyproconazole Substances 0.000 claims description 2
- 239000005758 Cyprodinil Substances 0.000 claims description 2
- 239000005767 Epoxiconazole Substances 0.000 claims description 2
- 239000005777 Fenpropidin Substances 0.000 claims description 2
- 239000005778 Fenpropimorph Substances 0.000 claims description 2
- 239000005785 Fluquinconazole Substances 0.000 claims description 2
- 239000005906 Imidacloprid Substances 0.000 claims description 2
- FKWDSATZSMJRLC-UHFFFAOYSA-N Iminoctadine acetate Chemical compound CC([O-])=O.CC([O-])=O.CC([O-])=O.NC([NH3+])=NCCCCCCCC[NH2+]CCCCCCCCN=C(N)[NH3+] FKWDSATZSMJRLC-UHFFFAOYSA-N 0.000 claims description 2
- 239000005800 Kresoxim-methyl Substances 0.000 claims description 2
- 239000005807 Metalaxyl Substances 0.000 claims description 2
- 239000005868 Metconazole Substances 0.000 claims description 2
- 239000005813 Penconazole Substances 0.000 claims description 2
- 239000005820 Prochloraz Substances 0.000 claims description 2
- 239000005822 Propiconazole Substances 0.000 claims description 2
- 239000005831 Quinoxyfen Substances 0.000 claims description 2
- 239000005837 Spiroxamine Substances 0.000 claims description 2
- 239000005839 Tebuconazole Substances 0.000 claims description 2
- LFVVNPBBFUSSHL-UHFFFAOYSA-N alexidine Chemical compound CCCCC(CC)CNC(=N)NC(=N)NCCCCCCNC(=N)NC(=N)NCC(CC)CCCC LFVVNPBBFUSSHL-UHFFFAOYSA-N 0.000 claims description 2
- 229950010221 alexidine Drugs 0.000 claims description 2
- WFDXOXNFNRHQEC-GHRIWEEISA-N azoxystrobin Chemical compound CO\C=C(\C(=O)OC)C1=CC=CC=C1OC1=CC(OC=2C(=CC=CC=2)C#N)=NC=N1 WFDXOXNFNRHQEC-GHRIWEEISA-N 0.000 claims description 2
- HAORKNGNJCEJBX-UHFFFAOYSA-N cyprodinil Chemical compound N=1C(C)=CC(C2CC2)=NC=1NC1=CC=CC=C1 HAORKNGNJCEJBX-UHFFFAOYSA-N 0.000 claims description 2
- WURGXGVFSMYFCG-UHFFFAOYSA-N dichlofluanid Chemical compound CN(C)S(=O)(=O)N(SC(F)(Cl)Cl)C1=CC=CC=C1 WURGXGVFSMYFCG-UHFFFAOYSA-N 0.000 claims description 2
- IJJVMEJXYNJXOJ-UHFFFAOYSA-N fluquinconazole Chemical compound C=1C=C(Cl)C=C(Cl)C=1N1C(=O)C2=CC(F)=CC=C2N=C1N1C=NC=N1 IJJVMEJXYNJXOJ-UHFFFAOYSA-N 0.000 claims description 2
- FQKUGOMFVDPBIZ-UHFFFAOYSA-N flusilazole Chemical compound C=1C=C(F)C=CC=1[Si](C=1C=CC(F)=CC=1)(C)CN1C=NC=N1 FQKUGOMFVDPBIZ-UHFFFAOYSA-N 0.000 claims description 2
- 229940056881 imidacloprid Drugs 0.000 claims description 2
- ZOTBXTZVPHCKPN-HTXNQAPBSA-N kresoxim-methyl Chemical compound CO\N=C(\C(=O)OC)C1=CC=CC=C1COC1=CC=CC=C1C ZOTBXTZVPHCKPN-HTXNQAPBSA-N 0.000 claims description 2
- XWPZUHJBOLQNMN-UHFFFAOYSA-N metconazole Chemical compound C1=NC=NN1CC1(O)C(C)(C)CCC1CC1=CC=C(Cl)C=C1 XWPZUHJBOLQNMN-UHFFFAOYSA-N 0.000 claims description 2
- ZQEIXNIJLIKNTD-UHFFFAOYSA-N methyl N-(2,6-dimethylphenyl)-N-(methoxyacetyl)alaninate Chemical compound COCC(=O)N(C(C)C(=O)OC)C1=C(C)C=CC=C1C ZQEIXNIJLIKNTD-UHFFFAOYSA-N 0.000 claims description 2
- 150000002780 morpholines Chemical class 0.000 claims description 2
- TVLSRXXIMLFWEO-UHFFFAOYSA-N prochloraz Chemical compound C1=CN=CN1C(=O)N(CCC)CCOC1=C(Cl)C=C(Cl)C=C1Cl TVLSRXXIMLFWEO-UHFFFAOYSA-N 0.000 claims description 2
- STJLVHWMYQXCPB-UHFFFAOYSA-N propiconazole Chemical compound O1C(CCC)COC1(C=1C(=CC(Cl)=CC=1)Cl)CN1N=CN=C1 STJLVHWMYQXCPB-UHFFFAOYSA-N 0.000 claims description 2
- PUYXTUJWRLOUCW-UHFFFAOYSA-N spiroxamine Chemical compound O1C(CN(CC)CCC)COC11CCC(C(C)(C)C)CC1 PUYXTUJWRLOUCW-UHFFFAOYSA-N 0.000 claims description 2
- HYVWIQDYBVKITD-UHFFFAOYSA-N tolylfluanid Chemical compound CN(C)S(=O)(=O)N(SC(F)(Cl)Cl)C1=CC=C(C)C=C1 HYVWIQDYBVKITD-UHFFFAOYSA-N 0.000 claims description 2
- -1 6-chloro-3-pyridinyl Chemical group 0.000 claims 3
- LDVVMCZRFWMZSG-OLQVQODUSA-N (3ar,7as)-2-(trichloromethylsulfanyl)-3a,4,7,7a-tetrahydroisoindole-1,3-dione Chemical compound C1C=CC[C@H]2C(=O)N(SC(Cl)(Cl)Cl)C(=O)[C@H]21 LDVVMCZRFWMZSG-OLQVQODUSA-N 0.000 claims 2
- 239000005745 Captan Substances 0.000 claims 2
- UELITFHSCLAHKR-UHFFFAOYSA-N acibenzolar-S-methyl Chemical compound CSC(=O)C1=CC=CC2=C1SN=N2 UELITFHSCLAHKR-UHFFFAOYSA-N 0.000 claims 2
- 150000003936 benzamides Chemical class 0.000 claims 2
- 229940117949 captan Drugs 0.000 claims 2
- TWFZGCMQGLPBSX-UHFFFAOYSA-N carbendazim Chemical compound C1=CC=C2NC(NC(=O)OC)=NC2=C1 TWFZGCMQGLPBSX-UHFFFAOYSA-N 0.000 claims 2
- RXDMAYSSBPYBFW-UHFFFAOYSA-N carpropamid Chemical compound C=1C=C(Cl)C=CC=1C(C)NC(=O)C1(CC)C(C)C1(Cl)Cl RXDMAYSSBPYBFW-UHFFFAOYSA-N 0.000 claims 2
- HKMOPYJWSFRURD-UHFFFAOYSA-N chloro hypochlorite;copper Chemical compound [Cu].ClOCl HKMOPYJWSFRURD-UHFFFAOYSA-N 0.000 claims 2
- FKLFBQCQQYDUAM-UHFFFAOYSA-N fenpiclonil Chemical compound ClC1=CC=CC(C=2C(=CNC=2)C#N)=C1Cl FKLFBQCQQYDUAM-UHFFFAOYSA-N 0.000 claims 2
- UYJUZNLFJAWNEZ-UHFFFAOYSA-N fuberidazole Chemical compound C1=COC(C=2NC3=CC=CC=C3N=2)=C1 UYJUZNLFJAWNEZ-UHFFFAOYSA-N 0.000 claims 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 2
- 150000003230 pyrimidines Chemical class 0.000 claims 2
- 239000011701 zinc Substances 0.000 claims 2
- 229910052725 zinc Inorganic materials 0.000 claims 2
- XERJKGMBORTKEO-VZUCSPMQSA-N (1e)-2-(ethylcarbamoylamino)-n-methoxy-2-oxoethanimidoyl cyanide Chemical compound CCNC(=O)NC(=O)C(\C#N)=N\OC XERJKGMBORTKEO-VZUCSPMQSA-N 0.000 claims 1
- WCXDHFDTOYPNIE-RIYZIHGNSA-N (E)-acetamiprid Chemical compound N#C/N=C(\C)N(C)CC1=CC=C(Cl)N=C1 WCXDHFDTOYPNIE-RIYZIHGNSA-N 0.000 claims 1
- HOKKPVIRMVDYPB-UVTDQMKNSA-N (Z)-thiacloprid Chemical compound C1=NC(Cl)=CC=C1CN1C(=N/C#N)/SCC1 HOKKPVIRMVDYPB-UVTDQMKNSA-N 0.000 claims 1
- PZBPKYOVPCNPJY-UHFFFAOYSA-N 1-[2-(allyloxy)-2-(2,4-dichlorophenyl)ethyl]imidazole Chemical compound ClC1=CC(Cl)=CC=C1C(OCC=C)CN1C=NC=C1 PZBPKYOVPCNPJY-UHFFFAOYSA-N 0.000 claims 1
- HJEVQOSZWIDFQJ-UHFFFAOYSA-N 2-(2h-triazol-4-yl)ethanol Chemical class OCCC1=CNN=N1 HJEVQOSZWIDFQJ-UHFFFAOYSA-N 0.000 claims 1
- ICSNLGPSRYBMBD-UHFFFAOYSA-N 2-aminopyridine Chemical compound NC1=CC=CC=N1 ICSNLGPSRYBMBD-UHFFFAOYSA-N 0.000 claims 1
- SOUGWDPPRBKJEX-UHFFFAOYSA-N 3,5-dichloro-N-(1-chloro-3-methyl-2-oxopentan-3-yl)-4-methylbenzamide Chemical compound ClCC(=O)C(C)(CC)NC(=O)C1=CC(Cl)=C(C)C(Cl)=C1 SOUGWDPPRBKJEX-UHFFFAOYSA-N 0.000 claims 1
- FSCWZHGZWWDELK-UHFFFAOYSA-N 3-(3,5-dichlorophenyl)-5-ethenyl-5-methyl-2,4-oxazolidinedione Chemical compound O=C1C(C)(C=C)OC(=O)N1C1=CC(Cl)=CC(Cl)=C1 FSCWZHGZWWDELK-UHFFFAOYSA-N 0.000 claims 1
- PCCSBWNGDMYFCW-UHFFFAOYSA-N 5-methyl-5-(4-phenoxyphenyl)-3-(phenylamino)-1,3-oxazolidine-2,4-dione Chemical compound O=C1C(C)(C=2C=CC(OC=3C=CC=CC=3)=CC=2)OC(=O)N1NC1=CC=CC=C1 PCCSBWNGDMYFCW-UHFFFAOYSA-N 0.000 claims 1
- 239000005875 Acetamiprid Substances 0.000 claims 1
- 239000005964 Acibenzolar-S-methyl Substances 0.000 claims 1
- 239000005752 Copper oxychloride Substances 0.000 claims 1
- 239000005756 Cymoxanil Substances 0.000 claims 1
- 239000005772 Famoxadone Substances 0.000 claims 1
- 239000005774 Fenamidone Substances 0.000 claims 1
- 239000005776 Fenhexamid Substances 0.000 claims 1
- 239000004606 Fillers/Extenders Substances 0.000 claims 1
- 239000005780 Fluazinam Substances 0.000 claims 1
- 239000005781 Fludioxonil Substances 0.000 claims 1
- 239000005786 Flutolanil Substances 0.000 claims 1
- 239000005789 Folpet Substances 0.000 claims 1
- 239000005791 Fuberidazole Substances 0.000 claims 1
- 239000005795 Imazalil Substances 0.000 claims 1
- 239000005867 Iprodione Substances 0.000 claims 1
- 239000005797 Iprovalicarb Substances 0.000 claims 1
- NWUWYYSKZYIQAE-ZBFHGGJFSA-N L-(R)-iprovalicarb Chemical compound CC(C)OC(=O)N[C@@H](C(C)C)C(=O)N[C@H](C)C1=CC=C(C)C=C1 NWUWYYSKZYIQAE-ZBFHGGJFSA-N 0.000 claims 1
- 241001484259 Lacuna Species 0.000 claims 1
- 239000005802 Mancozeb Substances 0.000 claims 1
- 239000005805 Mepanipyrim Substances 0.000 claims 1
- 239000005814 Pencycuron Substances 0.000 claims 1
- 239000005818 Picoxystrobin Substances 0.000 claims 1
- 239000005823 Propineb Substances 0.000 claims 1
- 239000005828 Pyrimethanil Substances 0.000 claims 1
- 239000005835 Silthiofam Substances 0.000 claims 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 1
- 239000005864 Sulphur Substances 0.000 claims 1
- 239000005940 Thiacloprid Substances 0.000 claims 1
- 239000005941 Thiamethoxam Substances 0.000 claims 1
- GNVMUORYQLCPJZ-UHFFFAOYSA-M Thiocarbamate Chemical compound NC([S-])=O GNVMUORYQLCPJZ-UHFFFAOYSA-M 0.000 claims 1
- 239000005847 Triazoxide Substances 0.000 claims 1
- 239000005857 Trifloxystrobin Substances 0.000 claims 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims 1
- 239000005863 Zoxamide Substances 0.000 claims 1
- METKIMKYRPQLGS-UHFFFAOYSA-N atenolol Chemical compound CC(C)NCC(O)COC1=CC=C(CC(N)=O)C=C1 METKIMKYRPQLGS-UHFFFAOYSA-N 0.000 claims 1
- RIOXQFHNBCKOKP-UHFFFAOYSA-N benomyl Chemical compound C1=CC=C2N(C(=O)NCCCC)C(NC(=O)OC)=NC2=C1 RIOXQFHNBCKOKP-UHFFFAOYSA-N 0.000 claims 1
- 150000001556 benzimidazoles Chemical class 0.000 claims 1
- IOJUPLGTWVMSFF-UHFFFAOYSA-N benzothiazole Chemical class C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 claims 1
- MITFXPHMIHQXPI-UHFFFAOYSA-N benzoxaprofen Natural products N=1C2=CC(C(C(O)=O)C)=CC=C2OC=1C1=CC=C(Cl)C=C1 MITFXPHMIHQXPI-UHFFFAOYSA-N 0.000 claims 1
- OIPMQULDKWSNGX-UHFFFAOYSA-N bis[[ethoxy(oxo)phosphaniumyl]oxy]alumanyloxy-ethoxy-oxophosphanium Chemical compound [Al+3].CCO[P+]([O-])=O.CCO[P+]([O-])=O.CCO[P+]([O-])=O OIPMQULDKWSNGX-UHFFFAOYSA-N 0.000 claims 1
- 239000006013 carbendazim Substances 0.000 claims 1
- 229960001591 cyfluthrin Drugs 0.000 claims 1
- QQODLKZGRKWIFG-QSFXBCCZSA-N cyfluthrin Chemical compound CC1(C)[C@@H](C=C(Cl)Cl)[C@H]1C(=O)O[C@@H](C#N)C1=CC=C(F)C(OC=2C=CC=CC=2)=C1 QQODLKZGRKWIFG-QSFXBCCZSA-N 0.000 claims 1
- BQYJATMQXGBDHF-UHFFFAOYSA-N difenoconazole Chemical compound O1C(C)COC1(C=1C(=CC(OC=2C=CC(Cl)=CC=2)=CC=1)Cl)CN1N=CN=C1 BQYJATMQXGBDHF-UHFFFAOYSA-N 0.000 claims 1
- AWZOLILCOUMRDG-UHFFFAOYSA-N edifenphos Chemical compound C=1C=CC=CC=1SP(=O)(OCC)SC1=CC=CC=C1 AWZOLILCOUMRDG-UHFFFAOYSA-N 0.000 claims 1
- 229960002125 enilconazole Drugs 0.000 claims 1
- 125000000219 ethylidene group Chemical group [H]C(=[*])C([H])([H])[H] 0.000 claims 1
- LMVPQMGRYSRMIW-KRWDZBQOSA-N fenamidone Chemical compound O=C([C@@](C)(N=C1SC)C=2C=CC=CC=2)N1NC1=CC=CC=C1 LMVPQMGRYSRMIW-KRWDZBQOSA-N 0.000 claims 1
- VDLGAVXLJYLFDH-UHFFFAOYSA-N fenhexamid Chemical compound C=1C=C(O)C(Cl)=C(Cl)C=1NC(=O)C1(C)CCCCC1 VDLGAVXLJYLFDH-UHFFFAOYSA-N 0.000 claims 1
- UZCGKGPEKUCDTF-UHFFFAOYSA-N fluazinam Chemical compound [O-][N+](=O)C1=CC(C(F)(F)F)=C(Cl)C([N+]([O-])=O)=C1NC1=NC=C(C(F)(F)F)C=C1Cl UZCGKGPEKUCDTF-UHFFFAOYSA-N 0.000 claims 1
- MUJOIMFVNIBMKC-UHFFFAOYSA-N fludioxonil Chemical compound C=12OC(F)(F)OC2=CC=CC=1C1=CNC=C1C#N MUJOIMFVNIBMKC-UHFFFAOYSA-N 0.000 claims 1
- PTCGDEVVHUXTMP-UHFFFAOYSA-N flutolanil Chemical compound CC(C)OC1=CC=CC(NC(=O)C=2C(=CC=CC=2)C(F)(F)F)=C1 PTCGDEVVHUXTMP-UHFFFAOYSA-N 0.000 claims 1
- HKIOYBQGHSTUDB-UHFFFAOYSA-N folpet Chemical compound C1=CC=C2C(=O)N(SC(Cl)(Cl)Cl)C(=O)C2=C1 HKIOYBQGHSTUDB-UHFFFAOYSA-N 0.000 claims 1
- 150000002357 guanidines Chemical class 0.000 claims 1
- 239000001257 hydrogen Substances 0.000 claims 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 1
- ONUFESLQCSAYKA-UHFFFAOYSA-N iprodione Chemical compound O=C1N(C(=O)NC(C)C)CC(=O)N1C1=CC(Cl)=CC(Cl)=C1 ONUFESLQCSAYKA-UHFFFAOYSA-N 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- CIFWZNRJIBNXRE-UHFFFAOYSA-N mepanipyrim Chemical compound CC#CC1=CC(C)=NC(NC=2C=CC=CC=2)=N1 CIFWZNRJIBNXRE-UHFFFAOYSA-N 0.000 claims 1
- 238000000034 method Methods 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- 229910052757 nitrogen Inorganic materials 0.000 claims 1
- COWNFYYYZFRNOY-UHFFFAOYSA-N oxazolidinedione Chemical compound O=C1COC(=O)N1 COWNFYYYZFRNOY-UHFFFAOYSA-N 0.000 claims 1
- OGYFATSSENRIKG-UHFFFAOYSA-N pencycuron Chemical compound C1=CC(Cl)=CC=C1CN(C(=O)NC=1C=CC=CC=1)C1CCCC1 OGYFATSSENRIKG-UHFFFAOYSA-N 0.000 claims 1
- 229910052698 phosphorus Inorganic materials 0.000 claims 1
- 239000011574 phosphorus Substances 0.000 claims 1
- XKJCHHZQLQNZHY-UHFFFAOYSA-N phthalimide Chemical class C1=CC=C2C(=O)NC(=O)C2=C1 XKJCHHZQLQNZHY-UHFFFAOYSA-N 0.000 claims 1
- IBSNKSODLGJUMQ-SDNWHVSQSA-N picoxystrobin Chemical compound CO\C=C(\C(=O)OC)C1=CC=CC=C1COC1=CC=CC(C(F)(F)F)=N1 IBSNKSODLGJUMQ-SDNWHVSQSA-N 0.000 claims 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 1
- QXJKBPAVAHBARF-BETUJISGSA-N procymidone Chemical compound O=C([C@]1(C)C[C@@]1(C1=O)C)N1C1=CC(Cl)=CC(Cl)=C1 QXJKBPAVAHBARF-BETUJISGSA-N 0.000 claims 1
- RMSLEMVTCJZJOC-UHFFFAOYSA-N propan-2-yl N-methoxy-2-[[2-[N-methoxy-C-(methylcarbamoyl)carbonimidoyl]phenyl]methoxyimino]ethanimidate Chemical compound CON=C(C=NOCC1=C(C=CC=C1)C(C(=O)NC)=NOC)OC(C)C RMSLEMVTCJZJOC-UHFFFAOYSA-N 0.000 claims 1
- KKMLIVYBGSAJPM-UHFFFAOYSA-L propineb Chemical compound [Zn+2].[S-]C(=S)NC(C)CNC([S-])=S KKMLIVYBGSAJPM-UHFFFAOYSA-L 0.000 claims 1
- HZRSNVGNWUDEFX-UHFFFAOYSA-N pyraclostrobin Chemical compound COC(=O)N(OC)C1=CC=CC=C1COC1=NN(C=2C=CC(Cl)=CC=2)C=C1 HZRSNVGNWUDEFX-UHFFFAOYSA-N 0.000 claims 1
- ZLIBICFPKPWGIZ-UHFFFAOYSA-N pyrimethanil Chemical compound CC1=CC(C)=NC(NC=2C=CC=CC=2)=N1 ZLIBICFPKPWGIZ-UHFFFAOYSA-N 0.000 claims 1
- XRJLAOUDSILTFT-UHFFFAOYSA-N pyroquilon Chemical compound O=C1CCC2=CC=CC3=C2N1CC3 XRJLAOUDSILTFT-UHFFFAOYSA-N 0.000 claims 1
- 150000003233 pyrroles Chemical class 0.000 claims 1
- FBQQHUGEACOBDN-UHFFFAOYSA-N quinomethionate Chemical compound N1=C2SC(=O)SC2=NC2=CC(C)=CC=C21 FBQQHUGEACOBDN-UHFFFAOYSA-N 0.000 claims 1
- 150000003254 radicals Chemical class 0.000 claims 1
- MXMXHPPIGKYTAR-UHFFFAOYSA-N silthiofam Chemical compound CC=1SC([Si](C)(C)C)=C(C(=O)NCC=C)C=1C MXMXHPPIGKYTAR-UHFFFAOYSA-N 0.000 claims 1
- 239000004094 surface-active agent Substances 0.000 claims 1
- NWWZPOKUUAIXIW-FLIBITNWSA-N thiamethoxam Chemical compound [O-][N+](=O)\N=C/1N(C)COCN\1CC1=CN=C(Cl)S1 NWWZPOKUUAIXIW-FLIBITNWSA-N 0.000 claims 1
- IQGKIPDJXCAMSM-UHFFFAOYSA-N triazoxide Chemical compound N=1C2=CC=C(Cl)C=C2[N+]([O-])=NC=1N1C=CN=C1 IQGKIPDJXCAMSM-UHFFFAOYSA-N 0.000 claims 1
- DQJCHOQLCLEDLL-UHFFFAOYSA-N tricyclazole Chemical compound CC1=CC=CC2=C1N1C=NN=C1S2 DQJCHOQLCLEDLL-UHFFFAOYSA-N 0.000 claims 1
- ONCZDRURRATYFI-TVJDWZFNSA-N trifloxystrobin Chemical compound CO\N=C(\C(=O)OC)C1=CC=CC=C1CO\N=C(/C)C1=CC=CC(C(F)(F)F)=C1 ONCZDRURRATYFI-TVJDWZFNSA-N 0.000 claims 1
- 150000003672 ureas Chemical class 0.000 claims 1
- 230000000694 effects Effects 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 241000607479 Yersinia pestis Species 0.000 description 1
- 150000007980 azole derivatives Chemical class 0.000 description 1
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical class OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- 230000003032 phytopathogenic effect Effects 0.000 description 1
Description
Fungicidally active compound combinations
The present invention relates to novel active compound combinations comprising a known halogenopyrimidine derivative and further known active compounds, which compositions are highly suitable for controlling phytopathogenic fungi.
It is already known that (2E/Z)-2-(2-{ [6-(3-chloro-2-methylphenoxy)-5-fluoro- 4-pyrimidinylJoxy}phenyl)-2-(methoxyimino)-N-methylethanamide has fungicidal properties (cf. EP-A1-937 050). The activity of this substance is good; however, at low application rates, it is sometimes unsatisfactory.
Furthermore, it is already known that numerous azole derivatives, aromatic carboxylic acid derivatives, morpholine compounds and other heterocycles can be used for controlling fungi (cf. K.H. Biichel "Pflanzenschutz und Schidlings- bekampfung” [Crop protection and pest control] pages 87, 136, 140, 141 and 146 to 153, Georg Thieme Verlag, Stuttgart 1977). However, the activity of the substances in question is not always satisfactory at low application rates.
It has now been found that the novel active compound combinations of compounds oo 20 of the formula (I)
NZ
ANS cl AN ! (1)
CH F 04 = N 3 H.C” ™N “CH, 0 and (1) ~~ 8-t-butyl-2-(N-ethyl-N-n-propyl-amino)-methyl-1,4-dioxaspiro-[5,4]-decane (reference: EP-A-0 281 842) of the formula
0)
CH,).C
CH-NZ (n)
C,H,n (spiroxamine) and/or (2) 5,7-dichloro-4-(4-fluorophenoxy)-quinoline (reference: EP-A-326 330) of the formula jog
Cl 0
RX an 2
Cl N ) (quinoxyfen) and/or 3) the triazole derivative (reference: EP-A-0 040 345) of the formula or o—{ Motz or g—ciony, (IV) \ Vi
N (tebuconazole) and/or
4) 1-[3-[4-(1,1 -dimethylethyl)phenyl]-2-methylpropyl]piperi dine (reference: DE-
A-2752 153) of the formula
N
(V)
CH, CH,
CH, oo
CH, (fenpropidin) and/or ®)) (+-)-cis-4-[3-[4-(1,1-dimethylethyl)phenyl]-2-methylpropyl]- 2,6-dimethylmorpholine (reference: DE-A-2 656 747) of the formula
H.C \
TO w oF CH, CH,
CH,
CH, CH, (fenpropimorph) : and/or (6) N-(l-cyano-1,2-dimethylpropyl)-2-(2,4-dichlorophenoxy)-propanamide (reference: EP-A 262 393) of the formula
Cl 0 CH, CH,
O (VI)
Ne
CH, CN
Cl (fenoxanil)
and/or : @)) tetrachloro-isophthalo-dinitrile (reference: US 3 290 353) of the formula
CN
Cl Cl (VII
Cl CN )
Cl (chlorothalonil) and/or (8) 1-(4-chloro-phenoxy)-3,3-dimethyl-1-(1,2,4-triazol-1-yl)-butan-2-one (reference: DE-A-2 201 063) of the formula
I a Dre-pr-c-oion, (1X)
Cp \ (triadimefon) \-/j and/or “9 1-(4-chloro-phenoxy)-3,3-dimethyl-1-(1,2,4-triazol-1-yl)-butan-2-ol (reference: DE-A-23 24 010) of the formula a - ¢ \ triadimenol
N // (triadimenol) and/or (10) the triazole (reference: EP-A-196 038) of the formula
N
[)
N{ {3
Q
OC Cl (xX)
F
(epoxiconazole) and/or (11) the triazole (reference: EP-A-329 397) of the formula
CH,
H,C
OH »
N 7 (XI)
Cl (metconazole) and/or
(12) the triazole (reference: EP-A-183 458) of the formula
Cl Cl 0 xr
AL (XII) = N
N~ SN” S \—=y (fluquinconazole) and/or (13) the triazole (reference: DE-A-3 406 993) of the formula
H,C
OH
Cl N \_ N (XIV) —N (cyproconazole) and/or (14) the triazole (reference: Pesticide Manual, 9th. Ed. (1991), page 654) of the formula fo
Cl I (XV)
NY (penconazole)
WJ and/or wo (15) the compound (reference: EP-A-253 213) of the formula
CH, or
OL — 0] (XVI)
H, c” SN
Oo
CH, (kresoxim-methyl) and/or (16) the compound (reference: EP-A-0 382 375) of the formula
NTN
ANA
CN HsCOL x 0CH; (xvi 1]
Oo (azoxystrobin) (17) the compound (reference: EP-A-0 310 550) of the formula : 15
CH,
N
{Hw H—{ \ (XVII) (cyprodinil) and/or
~ © 8 - (18) NN "-(iminodi-8,1-octanediyl)bis-guanidine triacetates (reference:
EP-A-155 509) of the formula + +
NH, NH,
HN—L N(CH, it, ry Hi, x3 CH,CO, (XIX) (iminoctadine triacetate) and/or (19) the triazole (reference: EP-A-068 813) of the formula
F
CH, ] & Ww, (xx)
N
NT S
\— (flusilazole)
N and/or (20) the imidazole derivative (reference: DE-A-2 429 523) of the formula
Cl
O ~~
NNN cl ci NPN (XX1) (prochloraz) and/or
(21) the triazole (reference: DE-A-2 551 560) of the formula
C,H, cl YY 0 ‘a (XX)
N=/
Cl (propiconazole) and/or 22) 1-(4-phenyl-phenoxy)-3,3-dimethyl-1-(1,2,4-triazol-1-yl)-butan-2-ol (reference: DE-A-2 324 010) of the formula 7 {OO o-gu-cn—enn oxi)
N
{ w) (bitertanol)
N and/or (23) 1-[(6-chloro-3-pyridinyl)-methyl]-N-nitro-2-imidazolidinimine (reference:
Pesticide Manual, 9th. Ed. (1991), page 491) of the formula
CH—y NH » Y (XXIV)
Cl N N—NO, (imidacloprid)
and/or (24) the aniline derivative (reference: DE-A-1 193 498) of the formula a5 _-S—CCI,F (XXV)
NG
SO;~N(CH,), (dichlofluanid) and/or (25) the aniline derivative (reference: DE-A-119 34 98) of the formula
H,C NL
SO;~N(CH,;), (tolylfluanid) and/or (26) the aniline derivative (reference: Pesticide Manual, 9th. Ed. (1991), page 554) of the formula
CH, THs _-CH—COOCH,
NG
(j~CHzO—CH, (XXVIII)
CH, Io) (metalaxyl) and/or
Claims (6)
1. Active compound combinations, comprising at least one compound of the formula NEN NS Cl AN (0 H CH F 04 = N
3 H.C” "N “CH, 0] and nH 8-t-butyl-2-(N-ethyl-N-n-propyl-amino)-methyl-1,4-dioxaspiro-[5,4]- decane (reference: EP-A-0 281 842) of the formula 0 CH CHz-N_ {ly C,H,n (spiroxamine) and/or (2) 5,7-dichloro-4-(4-fluorophenoxy)-quinoline (reference: EP-A-326 330) of the formula or Cl 0 NN (1 ~ Cl N (quinoxyfen) and/or 3) the triazole derivative (reference: EP-A-0 040 345) of the formula oH 0 _)-crronrc—con, (iV) Te _N N \_7 (tebuconazole) and/or 4) 1-[3-[4-(1,1-dimethylethyl)phenyl]-2-methylpropyl]piperidine (reference: DE-A-2 752 153) of the formula
N . (V) CH, CH, (fenpropidin) and/or h -120- (5) (+-)-cis-4-[3-[4-(1,1-dimethylethyl)phenyl}-2-methylpropyl]- 2,6-dimethylmorpholine (reference: DE-A-2 656 747) of the formula H,C YO V1 oy CH, CH, CH, CH, CH, (fenpropimorph) and/or
(6) N-(1-cyano-1,2-dimethylpropyl)-2-(2,4-dichlorophenoxy)-propane- amide (reference: EP-A 262 393) of the formula Cl 0] CH, CH, O (VII) NN Aa CH, CN cl (fenoxanil)
and/or @)) tetrachloro-isophthalo-dinitrile (reference: US 3 290 353) of the formula CN Ci Cl (vin Cl CN Cl (chlorothalonil)
S121 - and/or (8) 1-(4-chloro-phenoxy)-3,3-dimethyl-1-(1,2,4-triazol-1-yl)-butan-2-one (reference: DE-A-22 01 063) of the formula I a Dr-o-pr-c-cion, (1X) wl \ (triadimefon) N—2/ and/or €)) 1-(4-chloro-phenoxy)-3,3-dimethyl-1-(1,2,4-triazol-1-yl)-butan-2-ole . (reference: DE-A-2 324 010) of the formula ™ B —{ Dro-pr-cn—oion, X) A ¢ N (triadimenol) N and/or (10) the triazole (reference: EP-A-196 038) of the formula a -122- N [XN NQ I ¢ ) 0 C Cl (XI) F (epoxiconazole) and/or (11) the triazole (reference: EP-A-329 397) of the formula CH H,C ’ OH i»! N 7 (X11) Cl (metconazole)
and/or (12) the triazole (reference: EP-A-183 458) of the formula Cl Cl 0 : or JS (XH) _ N NT NT D, \—y (fluquinconazole)
and/or
(13) the triazole (reference: DE-A-3 406 993) of the formula H,C OH N Cl N” Di (XIV) \—\ (cyproconazole) and/or (14) the triazole (reference: Pesticide Manual, 9th.
Ed. (1991), page 654) of the formula a pron Cl I (XV) _N N \ 7 (penconazole)
and/or (15) the compound (reference: EP-A-253 213) of the formula
CH, CY Oo = 0) (XVI) H, c” NY 0) CH, (kresoxim-methyl) and/or oC S124 - (16) the compound (reference: EP-A-0 382 375) of the formula NEN NA CN HCO x OCH; (Xvi) 8 (azoxystrobin)
(17) the compound (reference: EP-A-0 310 550) of the formula CH, 7 \ ¢ Hw (XVII) N= (cyprodinil)
and/or
(18) N,N”-(iminodi-8,1-octanediyl)bis-guanidine triacetates (reference: EP-A-155 509) of the formula
+ + NH, NH, + - HNL N(CH) fir cry) N—LL ik, x3 CH,CO, (XIX) (iminoctadine triacetate)
and/or oC S125 - (19) the triazole (reference: EP-A-068 813) of the formula F CH, N ’ A; (flusilazole) —N and/or (20) the imidazole derivative (reference: DE-A-2 429 523) of the formula Cl 0) ad CH,
~\ . ol NN (XX) (prochloraz) and/or (21) the triazole (reference: DE-A-2 551 560) of the formula C,H, Ci oY 0 Jonze XXil) = Ci (propiconazole)
t S126 - and/or (22) 1-(4-phenyl-phenoxy)-3,3-dimethyl-1-(1,2,4-triazol-1-yl)-butan-2-ol (reference: DE-A-2 324 010) of the formula 7 OO Oopron—een, (XX) Cp bitertanol \ J ( ) and/or (23) 1-[(6-chloro-3-pyridinyl)-methyl}]-N-nitro-2-imidazolidinimine (reference: Pesticide Manual, 9th.
Ed. (1991), page 491) of the formula
~~ CH NH Y (XXIV) Cl N N—NO, (imidacloprid) and/or (24) the aniline derivative (reference: DE-A-1 193 498) of the formula a5 _S—CCl,F (XXV) NS SO;-N(CH,), (dichlofluanid)
and/or (25) the aniline derivative (reference: DE-A-119 34 98) of the formula H,C NL SOz-N(CH,), (tolylfluanid)
and/or
(26) the aniline derivative (reference: Pesticide Manual, 9th.
Ed. (1991), page 554) of the formula
CH, {Ms _-CH=COOCH, NG (CHO CH, (XXVIN) CH, 0) (metalaxyl)
and/or
(27) 4-(2,3-dichlorophenyl)-1H-pyrrole-3-carbonitrile (reference: EP-A-236 272) of the formula Cl Cl or (XXVIII) CN
(fenpiclonil)
and/or no -128- (28) the triazole derivative (reference: EP-A-112 284) of the formula
H.C 0 N cl © N~ Di TL \— © cl (XXIX) (difenconazole) and/or (29) the pyrrole derivative (reference: EP-A-206 999) of the formula ~S< 0 0 J NH (XXX) — ~~ NC (fludioxonil) : and/or (30) the benzimidazole derivative (reference: US-3 010 968) of the formula 0 N JL )—N ox N CH, (carbendazim)
and/or (31) the compound (reference: CASRN (3878-19-1)) of the formula H N (XXX) CIC a N 0) (fuberidazole)
and/or
(32) the imidazole derivative (reference: DE-A-2 063 857) of the formula OCH,CH=CH,, Cl N (XXX) Cl { py N (enilconazole)
and/or
(33) the imadizole derivative of the formula
0" Ci NZ = Na ANY (XXXIV)
+ (triazoxide)
(34) the compound (reference: DE-A-2 709 264) of the formula CN “N 1] (XXXV) Jo=cr(7co 0 Cl (cyfluthrin) F and/or (35) a guanidine derivative (reference: Pesticide Manual, 9th.
Ed. (1991), page 461) of the formula R® R® R*—N—(CH_)5[N—(CH,) l= N—H (XXXVI) H x (2 +m) CH,COO (euazatine)
in which m represents integers from 0 to 5 and
R3 represents hydrogen (17 to 23%) or the radical of the formula ~C=NH (77 to 83%), NH,
and/or (36) the benzothiadiazole derivative (reference: EP-A-0 313 512) of the formula N 8s’ _ s~ H,CS < (XXXVI) (acibenzolar S-methyl) and/or
) . (37) the urea derivative (reference: DE-A-2 732 257) of the formula 0 JL (XXXVI) N N H (pencycuron) Cl and/or (38) the benzamide derivative (reference: DE-A-2 731 522) of the formula
H . CF, O CH, (flutolanil)
i -132- and/or (39) the benzothiazole derivative (reference: DE-A-2 250 077) of the formula
CH, ZN XL N iy (XL) \ N S (tricyclazole) and/or
(40) the zinc propylene-1,2-bis-(dithiocarbamidate) (reference: Pesticide Manual, 9th.
Ed. (1991), page 726) of the formula i 3 —[Zn—8—C—NH—CH;—CH—NH—C—S]— XL) n>=1 (propineb)
and/or (41) the compound (reference: DE-A-2 012 656) of the formula CH, 0) cl N CH, (XLII) 0 (procymidone) Cl and/or (42) a thiocarbamate (reference: Pesticide Manual, 9th.
Ed. (1991)) of the formula H ,S N—&_ S< ( g—Me (XLII) N— < H 's (mancozeb) Me = mixture of Zn and Mn and/or (43) the phthalimide derivative (reference: Pesticide Manual, 9th.
Ed. (1991), page 431) of the formula
I C, STE (XLIV) I (folpet) 0) and/or
(44) the morpholine derivative (reference: EP-A-0 219 756) of the formula — © A »—c 0 N I CH=C \_/ - (XLV) OCH, (dimetomorph) OCH,
and/or
(45) the cyanoxime derivative (reference: Pesticide Manual, 9th.
Ed. (1991), page 206) of the formula nar CH;~CH;—NH—C—NH—C-C=NOCH, (XLVI) (cymoxanil)
and/or (46) the phosphorus compound (reference: Pesticide Manual, 9th.
Ed. (1991), page 443) of the formula HCO, 0 H ~o Al (XLVI) ° (fosetyl-Al)
and/or
(47) the oxazolidindione (reference: EP-A-0 393 911) of the formula CH, © NO (XLVIII) — (famoxadone) and/or (48) the pyrimidine derivative (reference: EP-A-0 270 111) of the formula CH, N Od N= XLIX) CH, (pyrimethanil)
: and/or (49) the pyrimidine derivative (reference: EP-A-0 270 111) of the formula OH N (_rose-on (L) ch (mepanipyrim) 3 and/or :
i - 136 - (50) the compound (reference: EP-A-0 472 996) of the formula i fHCH,), ©8yoH-0-G-i-Gr-oti-gr—_ =n, wy © CH; (iprovalicarb)
and/or (531) the aniline derivative (reference: EP-A-0 339 418 ) of the formula I ri Yon (LIT) CH, ]
Cl | Ci (fenhexamid)
and/or
(52) N-[1-(4-chloro-phenyl)-ethyl]-2,2-dichloro-1-ethyl-3-methyl-cyclo- propane-carboxamide (reference: EP-A-0 341 475) of the formula
J- Cl Cl oop LIII CH, s C,H; CH, (LIT) (carpropamid)
and/or
(53) the pyridinamine (reference: EP-A-0 031 257) of the formula cl H NO, CF; / \ N Cl —N (fluazinam) and/or (54) the dicarboxime derivative (reference: US-2 553 770) of the formula 0 SON —_ CCl, captan Y (captan) and/or (55) the compound (reference: DE-A-1 100 372) of the formula Na S =o LVI) ~ Ss
H.C N (chinomethionat) 8 and/or
(56) the compound (reference: EP-A-0 629 616) of the formula = N4 0] LVII bo, (LID)
(fenamidone) and/or
(57) the compound (reference: EP-A-376 279) of the formula
HN CH, cl S sno, (LVIID) ~ N y/ H N (chlothianidin)
and/or
(58) the compound (reference: EP-A-235 725) of the formula
N A\ N—CN o— —( (LIX) (_s (thiacloprid)
and/or
(59) the compound (reference: EP-A-580 553) of the formula 0 N nN A JN (LXD) HC” hd < - I (thiamethoxam) oN’ and/or (60) the compound (reference: WO-A-91-4965) of the formula N Cl = NA en (acetamiprid) CH, and/or (61) the compound (reference: EP-A-326 330) of the formula
F.C N 0) “ or (LXID) NS Oo = 0] H,C” “CH, (picoxystrobin). 0) and/or
(62) sulphur (LX1II) and/or (63) copper oxychloride (LXIV) and/or (64) the compound (reference: DE-A-2 149 923) of the formula
Ci 0) 0 LE on aw NT ny — H CH, (iprodione) Cl 0 and/or
(65) the compound (reference: DE-A-2 207 576) of the formula Cl ®) J /—CH, (LXV) N C, \ d CH, (vinclozolin) Ci [0] and/or
(66) the compound (reference: JP-A-575 584) of the formula Cl 0 Ci Oo (LXVII) Cl (phtalid) Cl and/or
(67) the compound (reference: DE-A-2 300 299) of the formula o
SJ (LX VIII) ~ °S N (edifenphos) CH, : and/or (68) the compound (reference:US-3 917 838) of the formula (LXIX) N 0] (pyroquilon)
and/or t -142 - (69) the hydroxyethyl-triazole derivative (reference: WO-A-96-16048) of the formula Cl 7 hry Cl CH, (LXX) NS LE and/or (70) the halogeno-benzimidazole (reference: WO-A-97-06171) of the formula S oO N > >—ci Fo N
H.C So, (LXXI) 7 \ Ti oO CH, and/or (71) the compound (reference: DE-A-196 02 095) of the formula Cl — )C (LXXII) Ny / O / YN Oo-N - H,C : and/or g S143 - (72) the benzamide derivative (reference: EP-A-0 600 629) of the formula Cl 0 CH re H,C NE I TH (LXXII0) cl CH, O (zoxamide) and/or (73) the compound (reference: EP-A-298 196) of the formula NC =n NZ — SQ: cl (LXXIV) NC H,C CH, (cyamidazosulfamid) CH, and/or (74) the compound (reference: WO-A-96 18631) of the formula
0
H.C CH, TE ee H,C S si Hy (silthiofam) ™ CH, CH,
N : (75) the compound (reference: EP-A-460 575) of the formula CH, ~Y oO. XO N CH 8 (LXXVI) O Id
H.C (trifloxystrobin) and/or (76) N-methyl-2-(methoxyimino)-2-[2-([1-(3-tri-fluoro-methyl-phenyl)- ethoxyliminomethyl)phenyl]acetamide (reference: EP-A-596 254) of ‘the formula Me NO 0 (LXXVID) CHZNH Ny OCH, Oo CF, and/or (77) 2-[2-([2-phenyl-2-methoxyimino-1-methylethyl]-imino-oxymethyl)- phenyl]-2-methoxyimino-N-methylacetamide (reference: WO-A-95-21154) of the formula
CH,
N 0. NHCH CH,0” Ne 3 Bh (LXXIID) OMe and/or (78) 2-[2-([2-(4-fluorophenyl)-2-methoxyimino-1-methylethylliminooxy- methyl)phenyl]-2-methoxyimino-N-methyl-acetamide (reference: WO-A-95-21154) of the formula CH,
H.C N N07 © 1 (LXXIX) OL =~ ~~ HC” SN CH, Oo F and/or (79) 2-[4-methoxy-3-(1-methylethoxy)-1,4-diazabuta-1,3-dienyl-oxy- methyl ]phenyl-2-methoximino-N-methyl-acetamide (reference: DE-A-19 528 651) of the formula H, H N Oo Co” RN XN H (LXXX) 0] OL ~ ~~ HC” ON CH, 0 and/or
J © 146 - (80) methyl N-(2-[1-(4-chlorophenyl)pyrazol-3-yloxymethyl]phenyl)-N- methoxycarbamate (reference: DE-A-44 23 612) of the formula N 0] cl NT (LXXXI) HyC~o” hi “CH, 0) and/or (81) 2,4-dihydro-5-methoxy-2-methyl-4-[2-([([1-(3-tri-fluoro-methyl- phenyl)ethylidene]amino)oxy]methyl)phenyl]-3H-1,2,4-triazol-3-ones (reference: WO-A-98-23155) of the formula — CH, x LO N~ ONO (LXXXII) me” CF, N—N_ CH, and/or (82) the compound of the formula
0) N N CH, gos N J—0—CH, Oo (LXXXII) (benomyl).
2. Active compound combination according to Claim 1, comprising a compound of the formula (I) and one of the compounds 1) to 81) in a mixing ratio of compound of the formula (I) to in each case one compound of the formulae (I) to (LXXXII) of 20:1 to 1:50 parts by weight.
3. Composition according to at least one of claims 1 and 2, characterized in that in the active compound combinations the weight ratio of active compound of the formula (I) to - active compound of group (1) is from 10:1 to 1:20, - active compound of group (2) is from 10:1 to 1:20, - active compound of group (3) is from 10:1 to 1:20, - active compound of group (4) is from 10:1 to 1:20, - active compound of group (5) is from 10:1 to 1:20, - active compound of group (6) is from 10:1 to 1:10, - active compound of group (7) is from 1:1 to 1:50, - active compound of group (8) is from 10:1 to 1:10, - active compound of group (9) is from 10:1 to 1:10, - active compound of group (10) is from 10:1 to 1:10, - active compound of group (11) is from 10:1 to 1:10, - active compound of group (12) is from 10:1 to 1:10, - active compound of group (13) is from 10:1 to 1:10, - active compound of group (14) is from 10:1 to 1:10, - active compound of group (15) is from 10:1 to 1:10, - active compound of group (16) is from 10:1 to 1:10, - active compound of group (17) is from 5:1 to 1:20, - active compound of group (18) is from 10:1 to 1:10, - active compound of group (19) is from 10:1 to 1:10, - active compound of group (20) is from 10:1 to 1:10, - active compound of group (21) is from 10:1 to 1:10, - active compound of group (22) is from 10:1 to 1:10,
ol 143. - active compound of group (23) is from 20:1 to 1:20, - active compound of group (24) is from 1:1 to 1:50, - active compound of group (25) is from 1:0,1 to 1:50, - active compound of group (26) is from 1:0,1 to 1:50, - active compound of group (27) is from 10:1 to 1:10, - active compound of group (28) is from 10:1 to 1:10, - active compound of group (29) is from 10:1 to 1:10, - active compound of group (30) is from 10:1 to 1:10, - active compound of group (31) is from 20:1 to 1:10, - active compound of group (32) is from 20:1 to 1:10, - active compound of group (33) is from 20:1 to 1:10, - active compound of group (34) is from 20:1 to 1:10, CL active compound of group (35) is from 10:1 to 1:10, - active compound of group (36) is from 50:1 to 1:50, - active compound of group (37) is from 10:1 to 1:10, - active compound of group (38) is from 10:1 to 1:10, ~ active compound of group (39) is from 10:1 to 1:10, - active compound of group (40) is from 1:1 to 1:50, - active compound of group (41) is from 10:1 to 1:10, - active compound of group (42) is from 1:1 to 1:50, - active compound of group (43) is from 1:1 to 1:50, - active compound of group (44) is from 10:1 to 1:10, - active compound of group (45) is from 10:1 to 1:10, - active compound of group (46) is from 10:1 to 1:50, - active compound of group (47) is from 10:1 to 1:10, | Co - active compound of group (48) is from 5:1 to 1:20, - active compound of group (49) is from 5:1 to 1:20, - active compound of group (50) is from 10:1 to 1:10, - active compound of group (51) is from 10:1 to 1:10, - active compound of group (52) is from 10:1 to 1:10, : - active compound of group (53) is from 10:1 to 1:10,
- active compound of group (54) is from 5:1 to 1:50, - active compound of group (55) is from 5:1 to 1:50, - active compound of group (56) is from 10:1 to 1:10, - active compound of group (57) is from 20:1 to 1:20, - active compound of group (58) is from 20:1 to 1:20, - active compound of group (59) is from 20:1 to 1:20, - active compound of group (60) is from 20:1 to 1:20, - active compound of group (61) is from 10:1 to 1:10, - active compound of group (62) is from 20:1 to 1:20, - active compound of group (63) is from 20:1 to 1:20, - active compound of group (64) is from 10:1 to 1:10, - active compound of group (65) is from 10:1 to 1:10, - active compound of group (66) is from 10:1 to 1:10, - active compound of group (67) is from 10:1 to 1:10, - active compound of group (68) is from 10:1 to 1:10, ~ - active compound of group (69) is from 20:1 to 1:5, - active compound of group (70) is from 50:1 to 1:10, - active compound of group (71) is from 10:1 to 1:10, - active compound of group (72) is from 50:1 to 1:10, - active compound of group (73) is from 20:1 to 1:5, - active compound of group (74) is from 20:1 to 1:10, - active compound of group (75) is from 10:1 to 1:10, - active compound of group (76) is from 10:1 to 1:10, - active compound of group (77) is from 10:1 to 1:10, : 25 - active compound of group (78) is from 10:1 to 1:10, - active compound of group (79) is from 10:1 to 1:10, - active compound of group (80) is from 10:1 to 1:10, - active compound of group (81) is from 10:1 to 1:10, - active compound of group (82) is from 10:1 to 1:10.
I oo -150 -
4. Method for controlling fungi, characterized in that active compound combinations according to any of Claims 1 to 3 [lacuna] to fungi and/or their habitat.
5. Use of active compound combinations according to at least one of Claims 1 to 3 for controlling fungi.
6. Process for preparing fungicidal compositions, characterized in that active compound combinations according to at least one of Claims 1 to 3 are mixed with extenders and/or surfactants.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10103832A DE10103832A1 (en) | 2000-05-11 | 2001-01-29 | Synergistic combination of fungicides for use in plant protection, comprises 2-(pyrimidinyloxy-phenyl)-2-(methoxyimino)-N-methyl-acetamide derivative and e.g. spiroxamine, quinoxyfen or tebuconazole |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ZA200208114B true ZA200208114B (en) | 2003-10-09 |
Family
ID=32518743
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ZA200208114A ZA200208114B (en) | 2001-01-29 | 2002-10-09 | Fungicidal combinations of active agents. |
Country Status (1)
| Country | Link |
|---|---|
| ZA (1) | ZA200208114B (en) |
-
2002
- 2002-10-09 ZA ZA200208114A patent/ZA200208114B/en unknown
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