BG107980A - Фунгицидни смеси - Google Patents
Фунгицидни смеси Download PDFInfo
- Publication number
- BG107980A BG107980A BG107980A BG10798003A BG107980A BG 107980 A BG107980 A BG 107980A BG 107980 A BG107980 A BG 107980A BG 10798003 A BG10798003 A BG 10798003A BG 107980 A BG107980 A BG 107980A
- Authority
- BG
- Bulgaria
- Prior art keywords
- formula
- compounds
- halogen
- mixtures
- alkyl
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 39
- 230000000855 fungicidal effect Effects 0.000 title claims abstract description 10
- 239000000417 fungicide Substances 0.000 title abstract description 4
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 15
- -1 benzothiazole-2-yl Chemical group 0.000 claims abstract description 14
- 150000002367 halogens Chemical class 0.000 claims abstract description 14
- 150000002460 imidazoles Chemical class 0.000 claims abstract description 10
- 238000000034 method Methods 0.000 claims abstract description 8
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 5
- 125000001637 1-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C(*)=C([H])C([H])=C([H])C2=C1[H] 0.000 claims abstract description 3
- 125000001622 2-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C(*)C([H])=C([H])C2=C1[H] 0.000 claims abstract description 3
- 241000233866 Fungi Species 0.000 claims description 11
- 239000007787 solid Substances 0.000 claims description 6
- XDEHMKQLKPZERH-BYPYZUCNSA-N (2s)-2-amino-3-methylbutanamide Chemical compound CC(C)[C@H](N)C(N)=O XDEHMKQLKPZERH-BYPYZUCNSA-N 0.000 claims description 5
- 239000000463 material Substances 0.000 claims description 4
- 239000002689 soil Substances 0.000 claims description 4
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 2
- 239000007788 liquid Substances 0.000 claims 2
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims 1
- 125000004190 benzothiazol-2-yl group Chemical group [H]C1=C([H])C([H])=C2N=C(*)SC2=C1[H] 0.000 claims 1
- 125000005843 halogen group Chemical group 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 abstract description 43
- 244000053095 fungal pathogen Species 0.000 abstract description 3
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract description 2
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract description 2
- 125000004093 cyano group Chemical group *C#N 0.000 abstract description 2
- 229940079865 intestinal antiinfectives imidazole derivative Drugs 0.000 abstract description 2
- 125000004498 isoxazol-4-yl group Chemical group O1N=CC(=C1)* 0.000 abstract description 2
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- 125000004663 dialkyl amino group Chemical group 0.000 abstract 1
- 241000196324 Embryophyta Species 0.000 description 17
- 239000013543 active substance Substances 0.000 description 16
- 238000005507 spraying Methods 0.000 description 7
- 230000002538 fungal effect Effects 0.000 description 5
- 101100352919 Caenorhabditis elegans ppm-2 gene Proteins 0.000 description 4
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- 235000013311 vegetables Nutrition 0.000 description 4
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 3
- 235000007688 Lycopersicon esculentum Nutrition 0.000 description 3
- 240000007594 Oryza sativa Species 0.000 description 3
- 235000007164 Oryza sativa Nutrition 0.000 description 3
- 241000233622 Phytophthora infestans Species 0.000 description 3
- 240000003768 Solanum lycopersicum Species 0.000 description 3
- 235000021307 Triticum Nutrition 0.000 description 3
- 244000098338 Triticum aestivum Species 0.000 description 3
- 239000000969 carrier Substances 0.000 description 3
- 235000013339 cereals Nutrition 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 229910052801 chlorine Inorganic materials 0.000 description 3
- 239000000460 chlorine Substances 0.000 description 3
- 239000003995 emulsifying agent Substances 0.000 description 3
- 239000008187 granular material Substances 0.000 description 3
- 150000002790 naphthalenes Chemical class 0.000 description 3
- 235000009566 rice Nutrition 0.000 description 3
- 239000000725 suspension Substances 0.000 description 3
- 230000002195 synergetic effect Effects 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 239000002023 wood Substances 0.000 description 3
- 235000000832 Ayote Nutrition 0.000 description 2
- 229920000742 Cotton Polymers 0.000 description 2
- 240000008067 Cucumis sativus Species 0.000 description 2
- 235000009849 Cucumis sativus Nutrition 0.000 description 2
- 241000219122 Cucurbita Species 0.000 description 2
- 235000009854 Cucurbita moschata Nutrition 0.000 description 2
- 235000009804 Cucurbita pepo subsp pepo Nutrition 0.000 description 2
- 240000005979 Hordeum vulgare Species 0.000 description 2
- 235000007340 Hordeum vulgare Nutrition 0.000 description 2
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
- 244000070406 Malus silvestris Species 0.000 description 2
- 240000005561 Musa balbisiana Species 0.000 description 2
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
- 240000000111 Saccharum officinarum Species 0.000 description 2
- 235000007201 Saccharum officinarum Nutrition 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 244000061456 Solanum tuberosum Species 0.000 description 2
- 235000002595 Solanum tuberosum Nutrition 0.000 description 2
- 241000607479 Yersinia pestis Species 0.000 description 2
- 235000021016 apples Nutrition 0.000 description 2
- 235000021015 bananas Nutrition 0.000 description 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 2
- 229910052794 bromium Inorganic materials 0.000 description 2
- 239000007859 condensation product Substances 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 238000010410 dusting Methods 0.000 description 2
- 235000013399 edible fruits Nutrition 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 239000003337 fertilizer Substances 0.000 description 2
- 235000013312 flour Nutrition 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 2
- PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical class C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 2
- 235000012015 potatoes Nutrition 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 235000015136 pumpkin Nutrition 0.000 description 2
- 238000009331 sowing Methods 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- XUJLWPFSUCHPQL-UHFFFAOYSA-N 11-methyldodecan-1-ol Chemical compound CC(C)CCCCCCCCCCO XUJLWPFSUCHPQL-UHFFFAOYSA-N 0.000 description 1
- PAWQVTBBRAZDMG-UHFFFAOYSA-N 2-(3-bromo-2-fluorophenyl)acetic acid Chemical compound OC(=O)CC1=CC=CC(Br)=C1F PAWQVTBBRAZDMG-UHFFFAOYSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- 239000004254 Ammonium phosphate Substances 0.000 description 1
- 244000105624 Arachis hypogaea Species 0.000 description 1
- 241000239290 Araneae Species 0.000 description 1
- 244000075850 Avena orientalis Species 0.000 description 1
- 235000007319 Avena orientalis Nutrition 0.000 description 1
- 241001480061 Blumeria graminis Species 0.000 description 1
- 241001465180 Botrytis Species 0.000 description 1
- 241000123650 Botrytis cinerea Species 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- 241000079253 Byssochlamys spectabilis Species 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 244000025254 Cannabis sativa Species 0.000 description 1
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 1
- 240000007154 Coffea arabica Species 0.000 description 1
- 241000371644 Curvularia ravenelii Species 0.000 description 1
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical class OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
- 241000510928 Erysiphe necator Species 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- 240000009088 Fragaria x ananassa Species 0.000 description 1
- 244000068988 Glycine max Species 0.000 description 1
- 235000010469 Glycine max Nutrition 0.000 description 1
- 241000896246 Golovinomyces cichoracearum Species 0.000 description 1
- 241000238631 Hexapoda Species 0.000 description 1
- 235000008694 Humulus lupulus Nutrition 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 239000005797 Iprovalicarb Substances 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 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 description 1
- 235000019738 Limestone Nutrition 0.000 description 1
- 241001330975 Magnaporthe oryzae Species 0.000 description 1
- 241000244206 Nematoda Species 0.000 description 1
- IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 1
- 241001668536 Oculimacula yallundae Species 0.000 description 1
- 241000736122 Parastagonospora nodorum Species 0.000 description 1
- 241000315044 Passalora arachidicola Species 0.000 description 1
- 244000046052 Phaseolus vulgaris Species 0.000 description 1
- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 241001281803 Plasmopara viticola Species 0.000 description 1
- 241000317981 Podosphaera fuliginea Species 0.000 description 1
- 241001337928 Podosphaera leucotricha Species 0.000 description 1
- 241000221300 Puccinia Species 0.000 description 1
- 241001361634 Rhizoctonia Species 0.000 description 1
- 206010039509 Scab Diseases 0.000 description 1
- 241000209056 Secale Species 0.000 description 1
- 235000007238 Secale cereale Nutrition 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 235000011941 Tilia x europaea Nutrition 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 241000221566 Ustilago Species 0.000 description 1
- 241000228452 Venturia inaequalis Species 0.000 description 1
- 240000006365 Vitis vinifera Species 0.000 description 1
- 235000014787 Vitis vinifera Nutrition 0.000 description 1
- 240000008042 Zea mays Species 0.000 description 1
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 1
- OMOVVBIIQSXZSZ-UHFFFAOYSA-N [6-(4-acetyloxy-5,9a-dimethyl-2,7-dioxo-4,5a,6,9-tetrahydro-3h-pyrano[3,4-b]oxepin-5-yl)-5-formyloxy-3-(furan-3-yl)-3a-methyl-7-methylidene-1a,2,3,4,5,6-hexahydroindeno[1,7a-b]oxiren-4-yl] 2-hydroxy-3-methylpentanoate Chemical compound CC12C(OC(=O)C(O)C(C)CC)C(OC=O)C(C3(C)C(CC(=O)OC4(C)COC(=O)CC43)OC(C)=O)C(=C)C32OC3CC1C=1C=COC=1 OMOVVBIIQSXZSZ-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 150000005215 alkyl ethers Chemical class 0.000 description 1
- 125000005037 alkyl phenyl group Chemical group 0.000 description 1
- 125000003275 alpha amino acid group Chemical group 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 229910000148 ammonium phosphate Inorganic materials 0.000 description 1
- 235000019289 ammonium phosphates Nutrition 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 125000001246 bromo group Chemical group Br* 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Inorganic materials [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 235000016213 coffee Nutrition 0.000 description 1
- 235000013353 coffee beverage Nutrition 0.000 description 1
- 235000005822 corn Nutrition 0.000 description 1
- MNNHAPBLZZVQHP-UHFFFAOYSA-N diammonium hydrogen phosphate Chemical compound [NH4+].[NH4+].OP([O-])([O-])=O MNNHAPBLZZVQHP-UHFFFAOYSA-N 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 description 1
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 1
- 239000010459 dolomite Substances 0.000 description 1
- 229910000514 dolomite Inorganic materials 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 239000003630 growth substance Substances 0.000 description 1
- 239000004009 herbicide Substances 0.000 description 1
- 238000004128 high performance liquid chromatography Methods 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 229910052745 lead Inorganic materials 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 239000006028 limestone Substances 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
- 235000012054 meals Nutrition 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 239000002420 orchard Substances 0.000 description 1
- 125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 description 1
- 230000001717 pathogenic effect Effects 0.000 description 1
- 235000020232 peanut Nutrition 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 238000010298 pulverizing process Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000011550 stock solution Substances 0.000 description 1
- 235000021012 strawberries Nutrition 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 229910021653 sulphate ion Inorganic materials 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 230000009885 systemic effect Effects 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 235000012222 talc Nutrition 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 238000009736 wetting Methods 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/50—1,3-Diazoles; Hydrogenated 1,3-diazoles
-
- 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
- A01N47/12—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing a —O—CO—N< group, or a thio analogue thereof, neither directly attached to a ring nor the nitrogen atom being a member of a heterocyclic ring
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)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE10102835 | 2001-01-22 | ||
PCT/EP2002/000497 WO2002056690A1 (de) | 2001-01-22 | 2002-01-19 | Fungizide mischungen |
Publications (1)
Publication Number | Publication Date |
---|---|
BG107980A true BG107980A (bg) | 2004-07-30 |
Family
ID=7671418
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
BG107980A BG107980A (bg) | 2001-01-22 | 2003-07-08 | Фунгицидни смеси |
Country Status (23)
Country | Link |
---|---|
US (1) | US7449195B2 (cs) |
EP (1) | EP1355531B1 (cs) |
JP (1) | JP2004522734A (cs) |
KR (1) | KR20030066819A (cs) |
CN (1) | CN100512645C (cs) |
AT (1) | ATE313260T1 (cs) |
BG (1) | BG107980A (cs) |
BR (1) | BR0206553A (cs) |
CA (1) | CA2435364C (cs) |
CZ (1) | CZ301672B6 (cs) |
DE (1) | DE50205340D1 (cs) |
EA (1) | EA006799B1 (cs) |
EE (1) | EE200300344A (cs) |
ES (1) | ES2254644T3 (cs) |
HU (1) | HUP0302728A3 (cs) |
IL (1) | IL156709A0 (cs) |
MX (1) | MXPA03006033A (cs) |
NZ (1) | NZ527474A (cs) |
PL (1) | PL205954B1 (cs) |
SK (1) | SK286121B6 (cs) |
UA (1) | UA74418C2 (cs) |
WO (1) | WO2002056690A1 (cs) |
ZA (1) | ZA200306514B (cs) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BRPI0509548A (pt) * | 2004-04-21 | 2007-09-18 | Basf Ag | misturas fungicidas para combater fungos nocivos fitopatogênicos, agente, processo para combater fungos nocivos fitopatogênicos, semente, e, uso dos compostos |
JP2008189658A (ja) * | 2007-01-12 | 2008-08-21 | Nissan Chem Ind Ltd | 植物病害の防除方法 |
CN103125509A (zh) * | 2013-04-06 | 2013-06-05 | 海利尔药业集团股份有限公司 | 一种含有苯噻菌胺与氰霜唑的杀菌组合物 |
Family Cites Families (22)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA1339133C (en) * | 1987-03-13 | 1997-07-29 | Rikuo Nasu | Imidazole compounds and biocidal composition comprising the same for controlling harmful organisms |
US5504109A (en) | 1989-05-13 | 1996-04-02 | Bayer Aktiengesellschaft | Susbstituted amino acid amide derivatives their preparation and use |
DE3915755A1 (de) | 1989-05-13 | 1990-11-29 | Bayer Ag | Fungizide mittel sowie substituierte aminosaeureamid-derivate und deren herstellung |
DE4304172A1 (de) * | 1993-02-12 | 1994-08-25 | Bayer Ag | Fungizide Wirkstoffkombinationen |
DE4321206A1 (de) | 1993-06-25 | 1995-01-05 | Bayer Ag | Fungizide Wirkstoffkombinationen |
DE4321897A1 (de) | 1993-07-01 | 1995-01-12 | Hoechst Schering Agrevo Gmbh | Substituierte Aminosäureamid-Derivate, Verfahren zu ihrer Herstellung, diese enthaltende Mittel und ihre Verwendung |
DE4431467A1 (de) | 1994-09-03 | 1996-03-07 | Basf Ag | Caramoylcarbonsäureamide |
DE19531814A1 (de) | 1995-08-30 | 1997-03-06 | Basf Ag | Carbamoylcarbonsäureamide |
ATE238308T1 (de) | 1995-08-10 | 2003-05-15 | Bayer Cropscience Ag | Halogenbenzimidazole und ihre verwendung als mikrobizide |
TW328945B (en) | 1995-08-30 | 1998-04-01 | Basf Ag | Carbamoylcarboxamides |
US5577976A (en) | 1995-08-31 | 1996-11-26 | General Motors Corporation | Power transmission |
JPH09323984A (ja) | 1996-06-04 | 1997-12-16 | Kumiai Chem Ind Co Ltd | アミノ酸アミド誘導体及び農園芸用殺菌剤 |
US6297236B1 (en) | 1998-04-06 | 2001-10-02 | Bayer Aktiengesellschaft | Fungicide active substance combinations |
DE19716256A1 (de) * | 1997-04-18 | 1998-10-22 | Bayer Ag | Fungizide Wirkstoffkombinationen |
US20020072535A1 (en) | 1997-04-18 | 2002-06-13 | Klaus Stenzel | Fungicide active substance combinations |
IL132435A (en) * | 1997-04-25 | 2005-03-20 | Ishihara Sangyo Kaisha | Composition for controlling harmful bio-organisms and method for controlling harmful bio-organisms using the same |
DE59907119D1 (de) | 1998-05-04 | 2003-10-30 | Basf Ag | Fungizide mischungen |
DE19904081A1 (de) | 1999-02-02 | 2000-08-03 | Bayer Ag | Fungizide Wirkstoffkombinationen |
JP4351789B2 (ja) | 1999-07-16 | 2009-10-28 | 石原産業株式会社 | 有害生物防除用組成物および有害生物の防除方法 |
HUP0203563A3 (en) * | 1999-12-13 | 2003-03-28 | Bayer Ag | Fungicidal combinations of active substances and use thereof |
DE10021412A1 (de) * | 1999-12-13 | 2001-06-21 | Bayer Ag | Fungizide Wirkstoffkombinationen |
JP2001181114A (ja) | 1999-12-27 | 2001-07-03 | Kumiai Chem Ind Co Ltd | 農園芸用殺菌剤組成物 |
-
2002
- 2002-01-19 EP EP02702285A patent/EP1355531B1/de not_active Expired - Lifetime
- 2002-01-19 CN CNB028037820A patent/CN100512645C/zh not_active Expired - Fee Related
- 2002-01-19 DE DE50205340T patent/DE50205340D1/de not_active Expired - Lifetime
- 2002-01-19 CZ CZ20031887A patent/CZ301672B6/cs not_active IP Right Cessation
- 2002-01-19 MX MXPA03006033A patent/MXPA03006033A/es active IP Right Grant
- 2002-01-19 JP JP2002557209A patent/JP2004522734A/ja active Pending
- 2002-01-19 IL IL15670902A patent/IL156709A0/xx unknown
- 2002-01-19 NZ NZ527474A patent/NZ527474A/en unknown
- 2002-01-19 CA CA2435364A patent/CA2435364C/en not_active Expired - Fee Related
- 2002-01-19 AT AT02702285T patent/ATE313260T1/de not_active IP Right Cessation
- 2002-01-19 SK SK900-2003A patent/SK286121B6/sk not_active IP Right Cessation
- 2002-01-19 US US10/466,397 patent/US7449195B2/en not_active Expired - Fee Related
- 2002-01-19 EE EEP200300344A patent/EE200300344A/xx unknown
- 2002-01-19 PL PL365819A patent/PL205954B1/pl not_active IP Right Cessation
- 2002-01-19 ES ES02702285T patent/ES2254644T3/es not_active Expired - Lifetime
- 2002-01-19 UA UA2003087911A patent/UA74418C2/uk unknown
- 2002-01-19 BR BR0206553-3A patent/BR0206553A/pt not_active IP Right Cessation
- 2002-01-19 HU HU0302728A patent/HUP0302728A3/hu unknown
- 2002-01-19 WO PCT/EP2002/000497 patent/WO2002056690A1/de active IP Right Grant
- 2002-01-19 KR KR10-2003-7009459A patent/KR20030066819A/ko not_active Withdrawn
- 2002-01-19 EA EA200300755A patent/EA006799B1/ru not_active IP Right Cessation
-
2003
- 2003-07-08 BG BG107980A patent/BG107980A/bg unknown
- 2003-08-21 ZA ZA200306514A patent/ZA200306514B/en unknown
Also Published As
Publication number | Publication date |
---|---|
US20040053980A1 (en) | 2004-03-18 |
JP2004522734A (ja) | 2004-07-29 |
EA200300755A1 (ru) | 2003-12-25 |
ES2254644T3 (es) | 2006-06-16 |
UA74418C2 (uk) | 2005-12-15 |
CA2435364C (en) | 2010-04-20 |
CN100512645C (zh) | 2009-07-15 |
SK286121B6 (sk) | 2008-04-07 |
PL365819A1 (en) | 2005-01-10 |
HUP0302728A3 (en) | 2005-11-28 |
EP1355531B1 (de) | 2005-12-21 |
US7449195B2 (en) | 2008-11-11 |
KR20030066819A (ko) | 2003-08-09 |
HUP0302728A2 (hu) | 2003-11-28 |
CA2435364A1 (en) | 2002-07-25 |
WO2002056690A1 (de) | 2002-07-25 |
ATE313260T1 (de) | 2006-01-15 |
PL205954B1 (pl) | 2010-06-30 |
DE50205340D1 (de) | 2006-01-26 |
BR0206553A (pt) | 2004-06-22 |
EE200300344A (et) | 2003-12-15 |
EP1355531A1 (de) | 2003-10-29 |
ZA200306514B (en) | 2004-09-06 |
MXPA03006033A (es) | 2003-09-10 |
SK9002003A3 (en) | 2003-12-02 |
IL156709A0 (en) | 2004-01-04 |
CN1525819A (zh) | 2004-09-01 |
EA006799B1 (ru) | 2006-04-28 |
CZ301672B6 (cs) | 2010-05-19 |
NZ527474A (en) | 2004-05-28 |
CZ20031887A3 (cs) | 2003-09-17 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
PL191033B1 (pl) | Mieszanina grzybobójcza | |
PL191907B1 (pl) | Mieszanina grzybobójcza | |
PL187352B1 (pl) | Mieszanina grzybobójcza | |
PL191155B1 (pl) | Mieszanina grzybobójcza | |
PL191333B1 (pl) | Mieszanina grzybobójcza | |
KR100504653B1 (ko) | 살진균성 혼합물 | |
KR20010013984A (ko) | 살진균제 혼합물 | |
JP2005511474A (ja) | 殺菌性混合物 | |
SK284885B6 (sk) | Fungicídne zmesi na báze pyridínamidov a fenarimolu a spôsob ničenia škodlivých húb | |
BG107980A (bg) | Фунгицидни смеси | |
BG107965A (bg) | Фунгицидни смеси от бензофенони и n-бифенилникотинамиди | |
KR20010052299A (ko) | 살진균성 혼합물 | |
PL195994B1 (pl) | Mieszanina grzybobójcza | |
KR100440846B1 (ko) | 살진균성 혼합물 | |
BG63185B1 (bg) | Фунгицидни смеси | |
PL181354B1 (pl) | Mieszanina grzybobójcza PL PL PL PL PL PL PL PL | |
JP4455330B2 (ja) | 殺菌混合物 | |
KR20010013094A (ko) | 살진균제 혼합물 | |
KR20030066815A (ko) | 살진균제 혼합물 | |
PL198430B1 (pl) | Mieszanina grzybobójcza | |
BG107858A (bg) | Фунгицидни смеси | |
MXPA98008776A (es) | Mezclas fungicidas | |
PL203421B1 (pl) | Mieszanina grzybobójcza, sposób zwalczania szkodliwych grzybów i srodek grzybobójczy |