PL84075B1 - - Google Patents
Download PDFInfo
- Publication number
- PL84075B1 PL84075B1 PL1972155893A PL15589372A PL84075B1 PL 84075 B1 PL84075 B1 PL 84075B1 PL 1972155893 A PL1972155893 A PL 1972155893A PL 15589372 A PL15589372 A PL 15589372A PL 84075 B1 PL84075 B1 PL 84075B1
- Authority
- PL
- Poland
- Prior art keywords
- formula
- compound
- radical
- active
- weight
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 claims description 38
- 241000196324 Embryophyta Species 0.000 claims description 34
- 239000013543 active substance Substances 0.000 claims description 34
- 239000004480 active ingredient Substances 0.000 claims description 18
- -1 alkyl radical Chemical class 0.000 claims description 16
- 230000012010 growth Effects 0.000 claims description 14
- 238000012360 testing method Methods 0.000 claims description 14
- 239000003795 chemical substances by application Substances 0.000 claims description 9
- 125000004432 carbon atom Chemical group C* 0.000 claims description 7
- 230000000855 fungicidal effect Effects 0.000 claims description 6
- 240000005979 Hordeum vulgare Species 0.000 claims description 5
- 235000007340 Hordeum vulgare Nutrition 0.000 claims description 5
- 239000000417 fungicide Substances 0.000 claims description 4
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 4
- 125000000217 alkyl group Chemical group 0.000 claims description 3
- 239000000969 carrier Substances 0.000 claims description 3
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims description 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 2
- 229910052794 bromium Inorganic materials 0.000 claims description 2
- 239000000460 chlorine Substances 0.000 claims description 2
- 229910052801 chlorine Inorganic materials 0.000 claims description 2
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- 239000011630 iodine Substances 0.000 claims description 2
- 229910052740 iodine Inorganic materials 0.000 claims description 2
- HRDXJKGNWSUIBT-UHFFFAOYSA-N methoxybenzene Chemical compound [CH2]OC1=CC=CC=C1 HRDXJKGNWSUIBT-UHFFFAOYSA-N 0.000 claims description 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 2
- 125000001424 substituent group Chemical group 0.000 claims description 2
- 239000004094 surface-active agent Substances 0.000 claims description 2
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical compound [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 claims 2
- 239000003899 bactericide agent Substances 0.000 claims 1
- 125000002883 imidazolyl group Chemical group 0.000 claims 1
- 239000000126 substance Substances 0.000 description 14
- 239000002904 solvent Substances 0.000 description 13
- 241000233866 Fungi Species 0.000 description 11
- 239000007788 liquid Substances 0.000 description 11
- 239000000203 mixture Substances 0.000 description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 11
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 10
- 244000141359 Malus pumila Species 0.000 description 7
- 235000011430 Malus pumila Nutrition 0.000 description 7
- 235000015103 Malus silvestris Nutrition 0.000 description 7
- 239000002689 soil Substances 0.000 description 7
- 206010033799 Paralysis Diseases 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 6
- 239000012141 concentrate Substances 0.000 description 6
- 239000003995 emulsifying agent Substances 0.000 description 6
- 239000003921 oil Substances 0.000 description 6
- 229920001817 Agar Polymers 0.000 description 5
- 235000001674 Agaricus brunnescens Nutrition 0.000 description 5
- 239000008272 agar Substances 0.000 description 5
- 239000000843 powder Substances 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- 239000007921 spray Substances 0.000 description 5
- HIXDQWDOVZUNNA-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one Chemical compound C=1C(OC)=CC(O)=C(C(C=2)=O)C=1OC=2C1=CC=C(OC)C(OC)=C1 HIXDQWDOVZUNNA-UHFFFAOYSA-N 0.000 description 4
- 241000223221 Fusarium oxysporum Species 0.000 description 4
- 206010061217 Infestation Diseases 0.000 description 4
- 125000002877 alkyl aryl group Chemical group 0.000 description 4
- 201000010099 disease Diseases 0.000 description 4
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- 238000011081 inoculation Methods 0.000 description 4
- 229920000151 polyglycol Polymers 0.000 description 4
- 239000010695 polyglycol Substances 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- 230000003449 preventive effect Effects 0.000 description 4
- 230000035939 shock Effects 0.000 description 4
- 239000000758 substrate Substances 0.000 description 4
- 241000894006 Bacteria Species 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 240000008067 Cucumis sativus Species 0.000 description 3
- 235000010799 Cucumis sativus var sativus Nutrition 0.000 description 3
- 206010014405 Electrocution Diseases 0.000 description 3
- 241000221787 Erysiphe Species 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 240000007594 Oryza sativa Species 0.000 description 3
- 235000007164 Oryza sativa Nutrition 0.000 description 3
- 206010039509 Scab Diseases 0.000 description 3
- 241001617088 Thanatephorus sasakii Species 0.000 description 3
- 230000000844 anti-bacterial effect Effects 0.000 description 3
- 239000002270 dispersing agent Substances 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- 239000012442 inert solvent Substances 0.000 description 3
- 239000002054 inoculum Substances 0.000 description 3
- 235000015097 nutrients Nutrition 0.000 description 3
- 238000010992 reflux Methods 0.000 description 3
- 235000009566 rice Nutrition 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 239000011877 solvent mixture Substances 0.000 description 3
- 241001450781 Bipolaris oryzae Species 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- 241000223194 Fusarium culmorum Species 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- MZRVEZGGRBJDDB-UHFFFAOYSA-N N-Butyllithium Chemical compound [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 description 2
- ATHHXGZTWNVVOU-UHFFFAOYSA-N N-methylformamide Chemical compound CNC=O ATHHXGZTWNVVOU-UHFFFAOYSA-N 0.000 description 2
- 229910002651 NO3 Inorganic materials 0.000 description 2
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 2
- 241000228454 Pyrenophora graminea Species 0.000 description 2
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 description 2
- 244000061456 Solanum tuberosum Species 0.000 description 2
- 235000002595 Solanum tuberosum Nutrition 0.000 description 2
- 241000561282 Thielaviopsis basicola Species 0.000 description 2
- 241000082085 Verticillium <Phyllachorales> Species 0.000 description 2
- 241000350580 Zenia Species 0.000 description 2
- 230000000895 acaricidal effect Effects 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 239000007900 aqueous suspension Substances 0.000 description 2
- 239000013068 control sample Substances 0.000 description 2
- 239000003085 diluting agent Substances 0.000 description 2
- 235000021186 dishes Nutrition 0.000 description 2
- 238000010410 dusting Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 150000002170 ethers Chemical class 0.000 description 2
- 230000002538 fungal effect Effects 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 239000008187 granular material Substances 0.000 description 2
- 230000009036 growth inhibition Effects 0.000 description 2
- 239000003630 growth substance Substances 0.000 description 2
- 230000035876 healing Effects 0.000 description 2
- 208000015181 infectious disease Diseases 0.000 description 2
- 125000000040 m-tolyl group Chemical group [H]C1=C([H])C(*)=C([H])C(=C1[H])C([H])([H])[H] 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 150000002902 organometallic compounds Chemical class 0.000 description 2
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 description 2
- 244000052769 pathogen Species 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- 150000003254 radicals Chemical class 0.000 description 2
- 210000003296 saliva Anatomy 0.000 description 2
- 238000009331 sowing Methods 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- NPZDCTUDQYGYQD-UHFFFAOYSA-N 1-tritylimidazole Chemical compound C1=NC=CN1C(C=1C=CC=CC=1)(C=1C=CC=CC=1)C1=CC=CC=C1 NPZDCTUDQYGYQD-UHFFFAOYSA-N 0.000 description 1
- NZZRRHNSHYCKJA-UHFFFAOYSA-N 2-(1h-pyrrol-2-ylsulfinyl)-1h-pyrrole Chemical compound C=1C=CNC=1S(=O)C1=CC=CN1 NZZRRHNSHYCKJA-UHFFFAOYSA-N 0.000 description 1
- 241000238876 Acari Species 0.000 description 1
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 1
- 241000223600 Alternaria Species 0.000 description 1
- 241000235349 Ascomycota Species 0.000 description 1
- 241001530056 Athelia rolfsii Species 0.000 description 1
- 241000221198 Basidiomycota Species 0.000 description 1
- 241000123650 Botrytis cinerea Species 0.000 description 1
- 241000219357 Cactaceae Species 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 241000407098 Colletotrichum coffeanum Species 0.000 description 1
- 241000221785 Erysiphales Species 0.000 description 1
- 239000004606 Fillers/Extenders Substances 0.000 description 1
- 241000879841 Fusarium oxysporum f. cubense Species 0.000 description 1
- 241000427940 Fusarium solani Species 0.000 description 1
- 241000489964 Fusicladium Species 0.000 description 1
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
- 241000896218 Golovinomyces orontii Species 0.000 description 1
- 101000873645 Homo sapiens Secretory carrier-associated membrane protein 3 Proteins 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- 241001459558 Monographella nivalis Species 0.000 description 1
- 241000131448 Mycosphaerella Species 0.000 description 1
- GXCLVBGFBYZDAG-UHFFFAOYSA-N N-[2-(1H-indol-3-yl)ethyl]-N-methylprop-2-en-1-amine Chemical compound CN(CCC1=CNC2=C1C=CC=C2)CC=C GXCLVBGFBYZDAG-UHFFFAOYSA-N 0.000 description 1
- 241001329956 Nothopassalora personata Species 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 241001494479 Pecora Species 0.000 description 1
- 239000001888 Peptone Substances 0.000 description 1
- 108010080698 Peptones Proteins 0.000 description 1
- 241000308483 Phialophora cinerescens Species 0.000 description 1
- 241000233614 Phytophthora Species 0.000 description 1
- 241001149949 Phytophthora cactorum Species 0.000 description 1
- 241001281803 Plasmopara viticola Species 0.000 description 1
- 241000896242 Podosphaera Species 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 241000184297 Pseudocercospora musae Species 0.000 description 1
- 235000014443 Pyrus communis Nutrition 0.000 description 1
- 241000813090 Rhizoctonia solani Species 0.000 description 1
- 241000220317 Rosa Species 0.000 description 1
- 241000277331 Salmonidae Species 0.000 description 1
- 241000221662 Sclerotinia Species 0.000 description 1
- 241000221696 Sclerotinia sclerotiorum Species 0.000 description 1
- 102100035895 Secretory carrier-associated membrane protein 3 Human genes 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 241000722093 Tilletia caries Species 0.000 description 1
- 241000317942 Venturia <ichneumonid wasp> Species 0.000 description 1
- 241000228452 Venturia inaequalis Species 0.000 description 1
- 241001223092 [Nectria] haematococca mpVI Species 0.000 description 1
- 239000000642 acaricide Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 230000004913 activation Effects 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 150000001346 alkyl aryl ethers Chemical class 0.000 description 1
- 229940045714 alkyl sulfonate alkylating agent Drugs 0.000 description 1
- 150000008052 alkyl sulfonates Chemical class 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 150000001491 aromatic compounds Chemical class 0.000 description 1
- 125000005228 aryl sulfonate group Chemical group 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 150000007514 bases Chemical class 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 150000008422 chlorobenzenes Chemical class 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000000110 cooling liquid Substances 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- 239000008121 dextrose Substances 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
- FPAFDBFIGPHWGO-UHFFFAOYSA-N dioxosilane;oxomagnesium;hydrate Chemical compound O.[Mg]=O.[Mg]=O.[Mg]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O FPAFDBFIGPHWGO-UHFFFAOYSA-N 0.000 description 1
- VKFAUCPBMAGVRG-UHFFFAOYSA-N dipivefrin hydrochloride Chemical compound [Cl-].C[NH2+]CC(O)C1=CC=C(OC(=O)C(C)(C)C)C(OC(=O)C(C)(C)C)=C1 VKFAUCPBMAGVRG-UHFFFAOYSA-N 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 235000013399 edible fruits Nutrition 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 238000003958 fumigation Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000004009 herbicide Substances 0.000 description 1
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 1
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 1
- 238000011534 incubation Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- 229920005610 lignin Polymers 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L magnesium chloride Substances [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 1
- 229910001629 magnesium chloride Inorganic materials 0.000 description 1
- CCERQOYLJJULMD-UHFFFAOYSA-M magnesium;carbanide;chloride Chemical compound [CH3-].[Mg+2].[Cl-] CCERQOYLJJULMD-UHFFFAOYSA-M 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 230000003641 microbiacidal effect Effects 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000004570 mortar (masonry) Substances 0.000 description 1
- XTEGVFVZDVNBPF-UHFFFAOYSA-L naphthalene-1,5-disulfonate(2-) Chemical compound C1=CC=C2C(S(=O)(=O)[O-])=CC=CC2=C1S([O-])(=O)=O XTEGVFVZDVNBPF-UHFFFAOYSA-L 0.000 description 1
- 230000017066 negative regulation of growth Effects 0.000 description 1
- 230000001069 nematicidal effect Effects 0.000 description 1
- 239000005645 nematicide Substances 0.000 description 1
- 210000000056 organ Anatomy 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 125000002524 organometallic group Chemical group 0.000 description 1
- 230000001717 pathogenic effect Effects 0.000 description 1
- 235000019319 peptone Nutrition 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 230000008635 plant growth Effects 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 230000008092 positive effect Effects 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 239000011814 protection agent Substances 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 238000000926 separation method Methods 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
- 239000002002 slurry Substances 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 230000028070 sporulation Effects 0.000 description 1
- 238000003892 spreading Methods 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 208000024891 symptom Diseases 0.000 description 1
- 238000003786 synthesis reaction Methods 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
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000008096 xylene 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
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/56—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/64—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms, e.g. histidine
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- 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 (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2128700A DE2128700C2 (de) | 1971-06-09 | 1971-06-09 | Fungitoxische Mittel |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PL84075B1 true PL84075B1 (en, 2012) | 1976-02-28 |
Family
ID=5810336
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PL1972155893A PL84075B1 (en, 2012) | 1971-06-09 | 1972-06-08 |
Country Status (24)
| Country | Link |
|---|---|
| US (1) | US3832466A (en, 2012) |
| JP (1) | JPS5751802B1 (en, 2012) |
| AT (1) | AT316209B (en, 2012) |
| BE (1) | BE784587A (en, 2012) |
| BR (1) | BR7203666D0 (en, 2012) |
| CA (1) | CA972287A (en, 2012) |
| CH (1) | CH531833A (en, 2012) |
| CS (1) | CS170188B2 (en, 2012) |
| DD (1) | DD103135A5 (en, 2012) |
| DE (1) | DE2128700C2 (en, 2012) |
| DK (1) | DK132054C (en, 2012) |
| EG (1) | EG10528A (en, 2012) |
| ES (1) | ES403651A1 (en, 2012) |
| FR (1) | FR2140622B1 (en, 2012) |
| GB (1) | GB1365634A (en, 2012) |
| HU (1) | HU164708B (en, 2012) |
| IE (1) | IE36407B1 (en, 2012) |
| IL (1) | IL39617A (en, 2012) |
| IT (1) | IT961223B (en, 2012) |
| MY (1) | MY7500051A (en, 2012) |
| NL (1) | NL176130C (en, 2012) |
| PL (1) | PL84075B1 (en, 2012) |
| TR (1) | TR18524A (en, 2012) |
| ZA (1) | ZA723937B (en, 2012) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2560512C2 (de) * | 1975-11-26 | 1984-11-15 | Bayer Ag, 5090 Leverkusen | Fungizides mittel |
| DE3307909A1 (de) * | 1983-03-05 | 1984-09-06 | Bayer Ag, 5090 Leverkusen | Fungizides mittel, verfahren zu dessen herstellung, sowie dessen verwendung |
| JPH03149404A (ja) * | 1989-10-31 | 1991-06-26 | Iseki & Co Ltd | 油圧装置 |
| JPH0385773U (en, 2012) * | 1989-12-14 | 1991-08-29 | ||
| JP2001039954A (ja) * | 1999-05-24 | 2001-02-13 | Tomono Agrica Co Ltd | ヘテロ環誘導体 |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1091103B (de) * | 1957-12-18 | 1960-10-20 | Basf Ag | Verfahren zur Herstellung von einen oder zwei stickstoffhaltige Reste und eine Kohlenstoff-Kohlenstoff-Dreifachbindung enthaltenden Verbindungen |
| US2971006A (en) * | 1959-12-11 | 1961-02-07 | Gen Aniline & Film Corp | 1-(-alkyl or -hydroxyalkyl)-1-(2-propynyl)-2-alkylimidazolinium halides |
| US3321366A (en) * | 1965-11-15 | 1967-05-23 | Dow Chemical Co | Fungicidal methods and compositions |
| US3479367A (en) * | 1966-10-03 | 1969-11-18 | Pfizer & Co C | 1-substituted-2-alkyl-5-nitroimidazoles |
| CH509040A (de) * | 1968-10-17 | 1971-06-30 | Ciba Geigy Ag | Schädlingsbekämpfungsmittel |
| BR6915465D0 (pt) * | 1969-03-07 | 1973-01-04 | Bayer Ag | Processo para preparar n-benzimidazois substituidos na posicao alfa por heterociclos penta-membrados com atividade antimicotica |
-
1971
- 1971-06-09 DE DE2128700A patent/DE2128700C2/de not_active Expired
-
1972
- 1972-05-26 US US00257365A patent/US3832466A/en not_active Expired - Lifetime
- 1972-05-29 EG EG216/72*UA patent/EG10528A/xx active
- 1972-06-01 CS CS3792A patent/CS170188B2/cs unknown
- 1972-06-06 IL IL39617A patent/IL39617A/xx unknown
- 1972-06-06 TR TR18524A patent/TR18524A/xx unknown
- 1972-06-07 BR BR3666/72A patent/BR7203666D0/pt unknown
- 1972-06-07 CH CH845372A patent/CH531833A/de not_active IP Right Cessation
- 1972-06-07 DD DD163511A patent/DD103135A5/xx unknown
- 1972-06-07 IT IT25369/72A patent/IT961223B/it active
- 1972-06-07 AT AT489772A patent/AT316209B/de not_active IP Right Cessation
- 1972-06-08 JP JP47056536A patent/JPS5751802B1/ja active Pending
- 1972-06-08 DK DK287472AA patent/DK132054C/da not_active IP Right Cessation
- 1972-06-08 IE IE796/72A patent/IE36407B1/xx unknown
- 1972-06-08 NL NLAANVRAGE7207797,A patent/NL176130C/xx not_active IP Right Cessation
- 1972-06-08 ES ES403651A patent/ES403651A1/es not_active Expired
- 1972-06-08 CA CA144,190A patent/CA972287A/en not_active Expired
- 1972-06-08 GB GB2674672A patent/GB1365634A/en not_active Expired
- 1972-06-08 PL PL1972155893A patent/PL84075B1/pl unknown
- 1972-06-08 ZA ZA723937A patent/ZA723937B/xx unknown
- 1972-06-08 BE BE784587A patent/BE784587A/xx not_active IP Right Cessation
- 1972-06-09 FR FR7220825A patent/FR2140622B1/fr not_active Expired
- 1972-06-09 HU HUBA2752A patent/HU164708B/hu unknown
-
1975
- 1975-12-30 MY MY51/75A patent/MY7500051A/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| ES403651A1 (es) | 1975-05-01 |
| IL39617A (en) | 1975-02-10 |
| BE784587A (fr) | 1972-12-08 |
| FR2140622A1 (en, 2012) | 1973-01-19 |
| DD103135A5 (en, 2012) | 1974-01-12 |
| ZA723937B (en) | 1973-03-28 |
| CH531833A (de) | 1972-12-31 |
| MY7500051A (en) | 1975-12-31 |
| HU164708B (en, 2012) | 1974-04-11 |
| DK132054B (en, 2012) | 1975-10-20 |
| IT961223B (it) | 1973-12-10 |
| DE2128700C2 (de) | 1985-04-25 |
| JPS5751802B1 (en, 2012) | 1982-11-04 |
| NL7207797A (en, 2012) | 1972-12-12 |
| BR7203666D0 (pt) | 1973-05-31 |
| NL176130C (nl) | 1985-03-01 |
| AT316209B (de) | 1974-06-25 |
| US3832466A (en) | 1974-08-27 |
| IL39617A0 (en) | 1972-08-30 |
| IE36407B1 (en) | 1976-10-27 |
| FR2140622B1 (en, 2012) | 1977-12-30 |
| CS170188B2 (en, 2012) | 1976-08-27 |
| IE36407L (en) | 1972-12-09 |
| EG10528A (en) | 1976-02-29 |
| TR18524A (tr) | 1977-03-04 |
| CA972287A (en) | 1975-08-05 |
| NL176130B (nl) | 1984-10-01 |
| DE2128700A1 (de) | 1973-01-04 |
| DK132054C (da) | 1977-06-20 |
| GB1365634A (en) | 1974-09-04 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| NO163306B (no) | Askorbat inferferens-motstandskomposisjon, proevemiddel ogfremgangsmaate for bestemmelse av peroksydativt aktive substanser. | |
| SU518105A3 (ru) | Фунгицид | |
| DK164157B (da) | Trialkyl- eller arylsulf(ox)oniumphosphinat-derivater med fungicid aktivitet, fremgangsmaade til fremstilling deraf samt fungicid- og/eller baktericidpraeparater indeholdende de aktive forbindelser og en fremgangsmaade til sygdomsbehandling af plantevaekster | |
| SU511832A3 (ru) | Фунгицид и микробицид | |
| JPH058161B2 (en, 2012) | ||
| PL84075B1 (en, 2012) | ||
| JPS63183570A (ja) | Ｎ−アルキル−２，６−ジメチルモルホリノカルボキシアミド塩及び該化合物を含有する殺菌剤 | |
| JPH01305064A (ja) | ２―フエニルスルフイニル―ニトロ―ピリジン類 | |
| US3069252A (en) | Methods for the control of the growth of plants and plant parts | |
| FI68498C (fi) | Blandning foer bekaempning av fytopatogeniska svampar och bakterier | |
| US4087534A (en) | N-haloalkylmio urazole pesticides | |
| US3518074A (en) | Benzoylcholine halides as plant growth stunting agents | |
| IL43840A (en) | Derivatives of 2-substituted 1,3,4-oxadiazole-5-thiol and fungicidal compositions containing them | |
| JPS6156208B2 (en, 2012) | ||
| US3766243A (en) | Ureidophenylisothioureas | |
| CS411386A2 (en) | Fungicide and method of its active substances production | |
| PL69661B1 (en, 2012) | ||
| SU849976A3 (ru) | Фунгицидоинсектицидное средство | |
| SU618019A3 (ru) | Фунгицидное средство | |
| CA1040204A (en) | Benzimidazole-1-carboximide acid esters | |
| SU655279A3 (ru) | Фунгицид | |
| HU206022B (en) | Fungicidal composition comprising imidazole derivative as active ingredient, process for producing the active ingredient and for applying the composition | |
| US4764433A (en) | Agent for the protection of materials | |
| DK158761B (da) | Fungicidt middel, anvendelse heraf til bekaempelse af svampe og som plantebeskyttelsesmiddel samt fremgangsmaade til bekaempelse af svampe | |
| US4344962A (en) | Sulphenylated acylurethanes and their use as fungicides |