SK38298A3 - Agent and method for combatting parasitic fungi - Google Patents

Agent and method for combatting parasitic fungi Download PDF

Info

Publication number: SK38298A3
Authority: SK; Slovakia
Prior art keywords: group; alkyl; phenyl; unsubstituted; halogen
Prior art date: 1995-09-25

Application number

SK382-98A

Other languages

English (en)

Slovak (sk)

Inventor

Herbert Bayer

Herbert Sauter

Eberhard Ammermann

Gisela Lorenz

Siegfried Strathmann

Harald Kohle

Gunter Retzlaff

Original Assignee

Basf Ag

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1995-09-25

Filing date

1996-09-12

Publication date

1998-11-04

1996-09-12 Application filed by Basf Ag filed Critical Basf Ag

1998-11-04 Publication of SK38298A3 publication Critical patent/SK38298A3/sk

Links

241000233866 Fungi Species 0.000 title claims abstract description 21
238000000034 method Methods 0.000 title claims description 8
230000003071 parasitic effect Effects 0.000 title abstract 2
150000001875 compounds Chemical class 0.000 claims abstract description 50
239000013543 active substance Substances 0.000 claims abstract description 30
102000018832 Cytochromes Human genes 0.000 claims abstract description 8
108010052832 Cytochromes Proteins 0.000 claims abstract description 8
230000029058 respiratory gaseous exchange Effects 0.000 claims abstract description 6
-1 mercapto, amino Chemical group 0.000 claims description 78
125000000217 alkyl group Chemical group 0.000 claims description 58
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 55
125000003118 aryl group Chemical group 0.000 claims description 41
239000000203 mixture Substances 0.000 claims description 40
125000001424 substituent group Chemical group 0.000 claims description 36
125000003545 alkoxy group Chemical group 0.000 claims description 35
229910052736 halogen Inorganic materials 0.000 claims description 27
150000002367 halogens Chemical group 0.000 claims description 27
125000004093 cyano group Chemical group *C#N 0.000 claims description 23
239000004480 active ingredient Substances 0.000 claims description 22
125000004414 alkyl thio group Chemical group 0.000 claims description 20
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 19
101150065749 Churc1 gene Proteins 0.000 claims description 18
125000001028 difluoromethyl group Chemical group [H]C(F)(F)* 0.000 claims description 18
125000004438 haloalkoxy group Chemical group 0.000 claims description 18
125000004663 dialkyl amino group Chemical group 0.000 claims description 16
125000003342 alkenyl group Chemical group 0.000 claims description 15
125000001188 haloalkyl group Chemical group 0.000 claims description 15
125000005843 halogen group Chemical group 0.000 claims description 15
125000004104 aryloxy group Chemical group 0.000 claims description 14
GVNVAWHJIKLAGL-UHFFFAOYSA-N 2-(cyclohexen-1-yl)cyclohexan-1-one Chemical compound O=C1CCCCC1C1=CCCCC1 GVNVAWHJIKLAGL-UHFFFAOYSA-N 0.000 claims description 13
102100038239 Protein Churchill Human genes 0.000 claims description 13
125000003282 alkyl amino group Chemical group 0.000 claims description 13
125000000304 alkynyl group Chemical group 0.000 claims description 13
125000000753 cycloalkyl group Chemical group 0.000 claims description 13
125000006323 alkenyl amino group Chemical group 0.000 claims description 11
125000001072 heteroaryl group Chemical group 0.000 claims description 10
125000000714 pyrimidinyl group Chemical group 0.000 claims description 10
229910052757 nitrogen Chemical group 0.000 claims description 9
239000007787 solid Substances 0.000 claims description 9
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical group N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 8
125000000623 heterocyclic group Chemical group 0.000 claims description 8
229910052717 sulfur Inorganic materials 0.000 claims description 8
125000003302 alkenyloxy group Chemical group 0.000 claims description 7
125000000000 cycloalkoxy group Chemical group 0.000 claims description 7
229910052760 oxygen Inorganic materials 0.000 claims description 7
125000004076 pyridyl group Chemical group 0.000 claims description 7
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 6
UUEVFMOUBSLVJW-UHFFFAOYSA-N oxo-[[1-[2-[2-[2-[4-(oxoazaniumylmethylidene)pyridin-1-yl]ethoxy]ethoxy]ethyl]pyridin-4-ylidene]methyl]azanium;dibromide Chemical group [Br-].[Br-].C1=CC(=C[NH+]=O)C=CN1CCOCCOCCN1C=CC(=C[NH+]=O)C=C1 UUEVFMOUBSLVJW-UHFFFAOYSA-N 0.000 claims description 6
239000001301 oxygen Substances 0.000 claims description 6
125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 6
239000011593 sulfur Chemical group 0.000 claims description 6
125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 5
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 5
239000007788 liquid Substances 0.000 claims description 5
125000003226 pyrazolyl group Chemical group 0.000 claims description 5
125000000335 thiazolyl group Chemical group 0.000 claims description 5
125000005842 heteroatom Chemical group 0.000 claims description 4
239000001257 hydrogen Substances 0.000 claims description 4
229910052739 hydrogen Inorganic materials 0.000 claims description 4
239000000463 material Substances 0.000 claims description 4
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 4
125000002971 oxazolyl group Chemical group 0.000 claims description 4
239000002689 soil Substances 0.000 claims description 4
125000001113 thiadiazolyl group Chemical group 0.000 claims description 4
125000004306 triazinyl group Chemical group 0.000 claims description 4
239000003795 chemical substances by application Substances 0.000 claims description 3
125000004122 cyclic group Chemical group 0.000 claims description 3
125000005844 heterocyclyloxy group Chemical group 0.000 claims description 3
125000004468 heterocyclylthio group Chemical group 0.000 claims description 3
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 2
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical group C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 2
125000005108 alkenylthio group Chemical group 0.000 claims description 2
125000000051 benzyloxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])O* 0.000 claims description 2
125000002619 bicyclic group Chemical group 0.000 claims description 2
125000006310 cycloalkyl amino group Chemical group 0.000 claims description 2
125000005366 cycloalkylthio group Chemical group 0.000 claims description 2
230000002538 fungal effect Effects 0.000 claims description 2
125000002541 furyl group Chemical group 0.000 claims description 2
150000002430 hydrocarbons Chemical group 0.000 claims description 2
125000002883 imidazolyl group Chemical group 0.000 claims description 2
125000000842 isoxazolyl group Chemical group 0.000 claims description 2
125000000962 organic group Chemical group 0.000 claims description 2
125000001715 oxadiazolyl group Chemical group 0.000 claims description 2
125000001820 oxy group Chemical group [*:1]O[*:2] 0.000 claims description 2
125000005702 oxyalkylene group Chemical group 0.000 claims description 2
125000000168 pyrrolyl group Chemical group 0.000 claims description 2
239000000126 substance Substances 0.000 claims description 2
125000001544 thienyl group Chemical group 0.000 claims description 2
125000001425 triazolyl group Chemical group 0.000 claims description 2
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
125000002102 aryl alkyloxo group Chemical group 0.000 claims 1
150000001721 carbon Chemical group 0.000 claims 1
229910052799 carbon Inorganic materials 0.000 claims 1
150000002431 hydrogen Chemical group 0.000 claims 1
DMYHGDXADUDKCQ-UHFFFAOYSA-N fenazaquin Chemical compound C1=CC(C(C)(C)C)=CC=C1CCOC1=NC=NC2=CC=CC=C12 DMYHGDXADUDKCQ-UHFFFAOYSA-N 0.000 abstract description 12
241001465180 Botrytis Species 0.000 abstract description 5
102000015782 Electron Transport Complex III Human genes 0.000 abstract description 2
108010024882 Electron Transport Complex III Proteins 0.000 abstract description 2
125000004432 carbon atom Chemical group C* 0.000 description 14
241000196324 Embryophyta Species 0.000 description 13
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 12
230000000694 effects Effects 0.000 description 12
239000005656 Fenazaquin Substances 0.000 description 10
230000002195 synergetic effect Effects 0.000 description 8
235000013399 edible fruits Nutrition 0.000 description 7
241000123650 Botrytis cinerea Species 0.000 description 6
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 6
150000008051 alkyl sulfates Chemical class 0.000 description 6
239000000460 chlorine Substances 0.000 description 6
239000006185 dispersion Substances 0.000 description 6
239000000417 fungicide Substances 0.000 description 6
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 5
239000000969 carrier Substances 0.000 description 5
239000003995 emulsifying agent Substances 0.000 description 5
239000000741 silica gel Substances 0.000 description 5
229910002027 silica gel Inorganic materials 0.000 description 5
206010061217 Infestation Diseases 0.000 description 4
241000209140 Triticum Species 0.000 description 4
235000021307 Triticum Nutrition 0.000 description 4
239000004359 castor oil Substances 0.000 description 4
235000019438 castor oil Nutrition 0.000 description 4
229910052801 chlorine Inorganic materials 0.000 description 4
125000000392 cycloalkenyl group Chemical group 0.000 description 4
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 4
239000011737 fluorine Substances 0.000 description 4
229910052731 fluorine Inorganic materials 0.000 description 4
230000000855 fungicidal effect Effects 0.000 description 4
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 4
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WHOZNOZYMBRCBL-OUKQBFOZSA-N (2E)-2-Tetradecenal Chemical compound CCCCCCCCCCC\C=C\C=O WHOZNOZYMBRCBL-OUKQBFOZSA-N 0.000 description 3
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 3
YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 3
FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 3
239000002253 acid Substances 0.000 description 3
150000001298 alcohols Chemical class 0.000 description 3
235000012211 aluminium silicate Nutrition 0.000 description 3
239000004202 carbamide Substances 0.000 description 3
125000004465 cycloalkenyloxy group Chemical group 0.000 description 3
229940052303 ethers for general anesthesia Drugs 0.000 description 3
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239000004009 herbicide Substances 0.000 description 3
125000004435 hydrogen atom Chemical group [H]* 0.000 description 3
229910052500 inorganic mineral Inorganic materials 0.000 description 3
239000011777 magnesium Substances 0.000 description 3
229910052749 magnesium Inorganic materials 0.000 description 3
239000011707 mineral Substances 0.000 description 3
239000002480 mineral oil Substances 0.000 description 3
235000010446 mineral oil Nutrition 0.000 description 3
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239000000377 silicon dioxide Substances 0.000 description 3
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239000002699 waste material Substances 0.000 description 3
HYZJCKYKOHLVJF-UHFFFAOYSA-N 1H-benzimidazole Chemical compound C1=CC=C2NC=NC2=C1 HYZJCKYKOHLVJF-UHFFFAOYSA-N 0.000 description 2
HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
125000004974 2-butenyl group Chemical group C(C=CC)* 0.000 description 2
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 2
125000006050 3-methyl-2-pentenyl group Chemical group 0.000 description 2
DLFVBJFMPXGRIB-UHFFFAOYSA-N Acetamide Chemical compound CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 description 2
239000005995 Aluminium silicate Substances 0.000 description 2
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240000004244 Cucurbita moschata Species 0.000 description 2
240000005979 Hordeum vulgare Species 0.000 description 2
235000007340 Hordeum vulgare Nutrition 0.000 description 2
244000070406 Malus silvestris Species 0.000 description 2
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
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WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 2
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125000001844 prenyl group Chemical group [H]C([*])([H])C([H])=C(C([H])([H])[H])C([H])([H])[H] 0.000 description 2
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239000004571 lime Substances 0.000 description 1
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239000000395 magnesium oxide Substances 0.000 description 1
CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
230000010534 mechanism of action Effects 0.000 description 1
ZWJNEYVWPYIKMB-UHFFFAOYSA-N methfuroxam Chemical compound CC1=C(C)OC(C)=C1C(=O)NC1=CC=CC=C1 ZWJNEYVWPYIKMB-UHFFFAOYSA-N 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
238000002156 mixing Methods 0.000 description 1
125000002757 morpholinyl group Chemical group 0.000 description 1
FTSDMYVLFMEZJS-UHFFFAOYSA-N n-(2,2,2-trichloroethyl)formamide Chemical compound ClC(Cl)(Cl)CNC=O FTSDMYVLFMEZJS-UHFFFAOYSA-N 0.000 description 1
OYRIKLVYHTWHCZ-UHFFFAOYSA-N n-cyclohexyl-2,5-dimethylfuran-3-carboxamide Chemical compound O1C(C)=CC(C(=O)NC2CCCCC2)=C1C OYRIKLVYHTWHCZ-UHFFFAOYSA-N 0.000 description 1
125000003136 n-heptyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 1
125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
150000002790 naphthalenes Chemical class 0.000 description 1
230000017074 necrotic cell death Effects 0.000 description 1
125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
150000002828 nitro derivatives Chemical class 0.000 description 1
239000000346 nonvolatile oil Substances 0.000 description 1
SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
235000014571 nuts Nutrition 0.000 description 1
125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000003921 oil Substances 0.000 description 1
ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
125000000160 oxazolidinyl group Chemical group 0.000 description 1
229960003540 oxyquinoline Drugs 0.000 description 1
239000012188 paraffin wax Substances 0.000 description 1
235000020232 peanut Nutrition 0.000 description 1
125000003538 pentan-3-yl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])[H] 0.000 description 1
239000000575 pesticide Substances 0.000 description 1
XYFCBTPGUUZFHI-UHFFFAOYSA-O phosphonium Chemical compound [PH4+] XYFCBTPGUUZFHI-UHFFFAOYSA-O 0.000 description 1
230000003032 phytopathogenic effect Effects 0.000 description 1
KNCYXPMJDCCGSJ-UHFFFAOYSA-N piperidine-2,6-dione Chemical compound O=C1CCCC(=O)N1 KNCYXPMJDCCGSJ-UHFFFAOYSA-N 0.000 description 1
125000003386 piperidinyl group Chemical group 0.000 description 1
239000005648 plant growth regulator Substances 0.000 description 1
239000004033 plastic Substances 0.000 description 1
229920003023 plastic Polymers 0.000 description 1
229920000570 polyether Polymers 0.000 description 1
229920001155 polypropylene Polymers 0.000 description 1
229940098458 powder spray Drugs 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
QXJKBPAVAHBARF-UHFFFAOYSA-N procymidone Chemical compound O=C1C2(C)CC2(C)C(=O)N1C1=CC(Cl)=CC(Cl)=C1 QXJKBPAVAHBARF-UHFFFAOYSA-N 0.000 description 1
235000015136 pumpkin Nutrition 0.000 description 1
JEXVQSWXXUJEMA-UHFFFAOYSA-N pyrazol-3-one Chemical compound O=C1C=CN=N1 JEXVQSWXXUJEMA-UHFFFAOYSA-N 0.000 description 1
125000003072 pyrazolidinyl group Chemical group 0.000 description 1
125000000719 pyrrolidinyl group Chemical group 0.000 description 1
MCJGNVYPOGVAJF-UHFFFAOYSA-N quinolin-8-ol Chemical compound C1=CN=C2C(O)=CC=CC2=C1 MCJGNVYPOGVAJF-UHFFFAOYSA-N 0.000 description 1
150000003254 radicals Chemical class 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
125000003548 sec-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
239000011734 sodium Substances 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
PYODKQIVQIVELM-UHFFFAOYSA-M sodium;2,3-bis(2-methylpropyl)naphthalene-1-sulfonate Chemical compound [Na+].C1=CC=C2C(S([O-])(=O)=O)=C(CC(C)C)C(CC(C)C)=CC2=C1 PYODKQIVQIVELM-UHFFFAOYSA-M 0.000 description 1
241000894007 species Species 0.000 description 1
125000005338 substituted cycloalkoxy group Chemical group 0.000 description 1
125000005346 substituted cycloalkyl group Chemical group 0.000 description 1
LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 1
125000004434 sulfur atom Chemical group 0.000 description 1
239000004094 surface-active agent Substances 0.000 description 1
235000012222 talc Nutrition 0.000 description 1
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
125000001973 tert-pentyl group Chemical group [H]C([H])([H])C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
125000003718 tetrahydrofuranyl group Chemical group 0.000 description 1
125000001984 thiazolidinyl group Chemical group 0.000 description 1
YFNCATAIYKQPOO-UHFFFAOYSA-N thiophanate Chemical compound CCOC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OCC YFNCATAIYKQPOO-UHFFFAOYSA-N 0.000 description 1
QGHREAKMXXNCOA-UHFFFAOYSA-N thiophanate-methyl Chemical compound COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC QGHREAKMXXNCOA-UHFFFAOYSA-N 0.000 description 1
KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 description 1
229960002447 thiram Drugs 0.000 description 1
DUBNHZYBDBBJHD-UHFFFAOYSA-L ziram Chemical compound [Zn+2].CN(C)C([S-])=S.CN(C)C([S-])=S DUBNHZYBDBBJHD-UHFFFAOYSA-L 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
- A01N43/54—1,3-Diazines; Hydrogenated 1,3-diazines

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)
Plural Heterocyclic Compounds (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Peptides Or Proteins (AREA)
Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
Enzymes And Modification Thereof (AREA)

SK382-98A 1995-09-25 1996-09-12 Agent and method for combatting parasitic fungi SK38298A3 (en)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
DE19535516		1995-09-25
PCT/EP1996/004013 WO1997011606A1 (fr)	1995-09-25	1996-09-12	Lutte contre des champignons nuisibles grace a l'association de la fenazaquine avec un principe actif inhibant la respiration au niveau du complexe cytochrome iii

Publications (1)

Publication Number	Publication Date
SK38298A3 true SK38298A3 (en)	1998-11-04

Family

ID=7773057

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SK382-98A SK38298A3 (en)	1995-09-25	1996-09-12	Agent and method for combatting parasitic fungi

Country Status (24)

Country	Link
US (2)	US6245771B1 (fr)
EP (1)	EP0862366B1 (fr)
JP (1)	JPH11511476A (fr)
KR (1)	KR19990063691A (fr)
CN (1)	CN1200651A (fr)
AR (1)	AR003693A1 (fr)
AT (1)	ATE208998T1 (fr)
AU (1)	AU711050B2 (fr)
BR (1)	BR9610700A (fr)
CA (1)	CA2230888A1 (fr)
CO (1)	CO4750755A1 (fr)
CZ (1)	CZ90098A3 (fr)
DE (1)	DE59608280D1 (fr)
HU (1)	HUP9900402A3 (fr)
IL (1)	IL123631A (fr)
IN (1)	IN1996CH01529A (fr)
NZ (1)	NZ319138A (fr)
PL (1)	PL326085A1 (fr)
RU (1)	RU2158083C1 (fr)
SK (1)	SK38298A3 (fr)
TW (1)	TW401275B (fr)
UA (1)	UA40670C2 (fr)
WO (1)	WO1997011606A1 (fr)
ZA (1)	ZA967963B (fr)

Families Citing this family (16)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CN1216439A (zh) *	1996-04-26	1999-05-12	巴斯福股份公司	杀菌混剂
SK144398A3 (en) *	1996-04-26	1999-04-13	Basf Ag	Fungicidal mixtures
KR20000049211A (ko) *	1996-10-17	2000-07-25	스타르크, 카르크	농작물에서의 유해 진균 방제법
EP1065928A1 (fr) *	1998-03-24	2001-01-10	Basf Aktiengesellschaft	Melanges fongicides a base de derives d'oximether de diatomite et de fongicides du riz
IL138125A0 (en) *	1998-03-24	2001-10-31	Basf Ag	Fungicidal mixtures based on tris (oxime ether) derivatives and resistance inducers
KR100557363B1 (ko) *	1998-03-24	2006-03-10	바스프 악티엔게젤샤프트	삼옥심에테르 유도체 및 다른 스트로빌루린을 기본으로하는 살진균제 혼합물
ID27443A (id) *	1998-03-24	2001-04-12	Basf Ag	Campuran fungisidal turunan-turunan dasar tris (oksim eter) dan fungisidal rhizoctonia
US6566349B1 (en)	2000-08-28	2003-05-20	Basf Corporation	Safer organophosphorous compositions
JP4804706B2 (ja) *	2003-05-20	2011-11-02	クミアイ化学工業株式会社	農園芸用殺菌剤組成物
US20050085922A1 (en) *	2003-10-17	2005-04-21	Shappley Ben R.	Shaped filler for implantation into a bone void and methods of manufacture and use thereof
CN1305858C (zh)	2004-02-20	2007-03-21	沈阳化工研究院	取代唑类化合物及其制备与应用
CN101755769B (zh) *	2009-08-12	2013-03-20	东莞市瑞德丰生物科技有限公司	一种含有喹螨醚的增效农药组合物
CN101653120B (zh) *	2009-08-12	2012-12-19	东莞市瑞德丰生物科技有限公司	一种含有喹螨醚的杀螨组合物
CN101669479B (zh) *	2009-10-16	2012-12-05	深圳诺普信农化股份有限公司	一种杀螨组合物
EP3031325A1 (fr)	2014-12-10	2016-06-15	Basf Se	Procédé de lutte contre la rouille du soja comprenant le traitement du soja avec des (2E)-2-[2-[[1-(2,4-substitués-phényl)pyrazol-3-yl]oxyméthyl]-3-substitués phényl]-2-méthoxyimino-n-méthyl-acétamides
EP3047731A1 (fr)	2015-01-21	2016-07-27	Basf Se	Procédé de lutte contre la rouille du soja comprenant le traitement du soja avec des (2E)-2-[3-substitués-2 [[(E)-[(2E)-2-alkoxyimino-1-méthyl-2-phényl-ethylidene]amino]oxyméthyl]phényl]-2-méthoxy-imino-N-méthyl-acétamides

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
IL89027A (en) *	1988-01-29	1993-01-31	Lilly Co Eli	Quinazoline derivatives, process for their preparation and fungicidal, insecticidal and miticidal compositions containing them
GB8903019D0 (en) *	1989-02-10	1989-03-30	Ici Plc	Fungicides
ATE141589T1 (de) *	1989-05-17	1996-09-15	Shionogi & Co	Alkoxyiminoacetamid-derivate und ihre verwendung als pilztötendes mittel
US5436248A (en) *	1993-07-02	1995-07-25	Ciba-Geigy Corporation	Microbicides
JP3634409B2 (ja)	1993-09-13	2005-03-30	ビーエーエスエフアクチェンゲゼルシャフト	殺菌剤混合物
US5491231A (en)	1994-11-28	1996-02-13	American Home Products Corporation	Hindered N-oxide esters of rapamycin
JP3680304B2 (ja)	1995-01-20	2005-08-10	日本曹達株式会社	作用点の異なる呼吸阻害剤からなる農園芸用殺菌剤
CN1216439A (zh)	1996-04-26	1999-05-12	巴斯福股份公司	杀菌混剂

1996
- 1996-08-30 TW TW085110597A patent/TW401275B/zh not_active IP Right Cessation
- 1996-09-12 EP EP96932515A patent/EP0862366B1/fr not_active Expired - Lifetime
- 1996-09-12 AU AU71288/96A patent/AU711050B2/en not_active Ceased
- 1996-09-12 UA UA98042077A patent/UA40670C2/uk unknown
- 1996-09-12 PL PL96326085A patent/PL326085A1/xx unknown
- 1996-09-12 CZ CZ98900A patent/CZ90098A3/cs unknown
- 1996-09-12 HU HU9900402A patent/HUP9900402A3/hu unknown
- 1996-09-12 IL IL12363196A patent/IL123631A/xx not_active IP Right Cessation
- 1996-09-12 JP JP9513110A patent/JPH11511476A/ja active Pending
- 1996-09-12 NZ NZ319138A patent/NZ319138A/xx unknown
- 1996-09-12 US US09/029,951 patent/US6245771B1/en not_active Expired - Fee Related
- 1996-09-12 RU RU98108416/04A patent/RU2158083C1/ru active
- 1996-09-12 IN IN1529CH1996 patent/IN1996CH01529A/en unknown
- 1996-09-12 WO PCT/EP1996/004013 patent/WO1997011606A1/fr not_active Ceased
- 1996-09-12 CN CN96197804A patent/CN1200651A/zh active Pending
- 1996-09-12 KR KR1019980702157A patent/KR19990063691A/ko not_active Abandoned
- 1996-09-12 CA CA002230888A patent/CA2230888A1/fr not_active Abandoned
- 1996-09-12 DE DE59608280T patent/DE59608280D1/de not_active Expired - Lifetime
- 1996-09-12 BR BR9610700A patent/BR9610700A/pt unknown
- 1996-09-12 SK SK382-98A patent/SK38298A3/sk unknown
- 1996-09-12 AT AT96932515T patent/ATE208998T1/de not_active IP Right Cessation
- 1996-09-20 ZA ZA9607963A patent/ZA967963B/xx unknown
- 1996-09-24 AR ARP960104467A patent/AR003693A1/es unknown
- 1996-09-25 CO CO96051133A patent/CO4750755A1/es unknown
2000
- 2000-05-15 US US09/571,402 patent/US6274586B1/en not_active Expired - Fee Related

Also Published As

Publication number	Publication date
IN1996CH01529A (fr)	2005-03-04
DE59608280D1 (de)	2002-01-03
MX9802272A (es)	1998-08-30
HUP9900402A3 (en)	2000-06-28
TW401275B (en)	2000-08-11
CA2230888A1 (fr)	1997-04-03
ATE208998T1 (de)	2001-12-15
AR003693A1 (es)	1998-09-09
US6245771B1 (en)	2001-06-12
CZ90098A3 (cs)	1998-08-12
RU2158083C2 (en)	2000-10-27
UA40670C2 (uk)	2001-08-15
IL123631A (en)	2000-11-21
CO4750755A1 (es)	1999-03-31
HUP9900402A2 (hu)	1999-05-28
IL123631A0 (en)	1998-10-30
WO1997011606A1 (fr)	1997-04-03
RU2158083C1 (ru)	2000-10-27
AU711050B2 (en)	1999-10-07
NZ319138A (en)	1999-11-29
KR19990063691A (ko)	1999-07-26
AU7128896A (en)	1997-04-17
BR9610700A (pt)	1999-07-13
ZA967963B (en)	1998-03-20
US6274586B1 (en)	2001-08-14
EP0862366B1 (fr)	2001-11-21
EP0862366A1 (fr)	1998-09-09
PL326085A1 (en)	1998-08-17
CN1200651A (zh)	1998-12-02
JPH11511476A (ja)	1999-10-05

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