DD240494A5 - Pestizide zusammensetzung - Google Patents

Pestizide zusammensetzung Download PDF

Info

Publication number: DD240494A5
Authority: DD; German Democratic Republic
Prior art keywords: optionally substituted; radical; active material; halogen atoms; plants
Prior art date: 1984-10-26

Application number

DD85282073A

Other languages

German (de)

English (en)

Inventor

Raymond Giraudon

Georges Santini

Original Assignee

��`��@��k��

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.)

1984-10-26

Filing date

1985-10-25

Publication date

1986-11-05

1985-10-25 Application filed by ��`��@��k�� filed Critical ��`��@��k��

1986-11-05 Publication of DD240494A5 publication Critical patent/DD240494A5/de

Links

239000000203 mixture Substances 0.000 title claims abstract description 30
239000000575 pesticide Substances 0.000 title description 2
239000011149 active material Substances 0.000 claims abstract description 21
VEKMJKMSTPFHQD-UHFFFAOYSA-N 1h-benzimidazole-2-carbonitrile Chemical class C1=CC=C2NC(C#N)=NC2=C1 VEKMJKMSTPFHQD-UHFFFAOYSA-N 0.000 claims abstract description 15
239000004094 surface-active agent Substances 0.000 claims abstract description 9
230000000361 pesticidal effect Effects 0.000 claims abstract description 8
150000001875 compounds Chemical class 0.000 claims description 30
238000000034 method Methods 0.000 claims description 15
125000005843 halogen group Chemical group 0.000 claims description 11
241000233866 Fungi Species 0.000 claims description 9
125000000217 alkyl group Chemical group 0.000 claims description 7
229910052757 nitrogen Inorganic materials 0.000 claims description 7
125000004433 nitrogen atom Chemical group N* 0.000 claims description 5
230000003032 phytopathogenic effect Effects 0.000 claims description 5
125000001424 substituent group Chemical group 0.000 claims description 4
238000011282 treatment Methods 0.000 claims description 4
125000003545 alkoxy group Chemical group 0.000 claims description 3
125000004432 carbon atom Chemical group C* 0.000 claims description 3
125000004093 cyano group Chemical group *C#N 0.000 claims description 3
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 3
125000003302 alkenyloxy group Chemical group 0.000 claims description 2
125000005108 alkenylthio group Chemical group 0.000 claims description 2
125000004414 alkyl thio group Chemical group 0.000 claims description 2
125000005133 alkynyloxy group Chemical group 0.000 claims description 2
125000005109 alkynylthio group Chemical group 0.000 claims description 2
MDFFNEOEWAXZRQ-UHFFFAOYSA-N aminyl Chemical compound [NH2] MDFFNEOEWAXZRQ-UHFFFAOYSA-N 0.000 claims description 2
125000004429 atom Chemical group 0.000 claims description 2
125000000623 heterocyclic group Chemical group 0.000 claims description 2
241000153246 Anteros Species 0.000 claims 1
230000000843 anti-fungal effect Effects 0.000 abstract description 3
239000004480 active ingredient Substances 0.000 abstract description 2
-1 alkoxy radicals Chemical class 0.000 description 20
241000196324 Embryophyta Species 0.000 description 16
KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 12
239000000843 powder Substances 0.000 description 9
239000002904 solvent Substances 0.000 description 9
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 7
150000004820 halides Chemical class 0.000 description 7
239000007787 solid Substances 0.000 description 7
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 6
241000227653 Lycopersicon Species 0.000 description 5
229910052783 alkali metal Inorganic materials 0.000 description 5
150000001340 alkali metals Chemical class 0.000 description 5
239000000839 emulsion Substances 0.000 description 5
239000007788 liquid Substances 0.000 description 5
150000003839 salts Chemical class 0.000 description 5
239000000243 solution Substances 0.000 description 5
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 4
239000002253 acid Substances 0.000 description 4
239000000654 additive Substances 0.000 description 4
239000004495 emulsifiable concentrate Substances 0.000 description 4
125000004435 hydrogen atom Chemical class [H]* 0.000 description 4
150000003254 radicals Chemical class 0.000 description 4
239000003381 stabilizer Substances 0.000 description 4
239000000725 suspension Substances 0.000 description 4
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 3
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 3
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
238000005481 NMR spectroscopy Methods 0.000 description 3
235000002637 Nicotiana tabacum Nutrition 0.000 description 3
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
239000000370 acceptor Substances 0.000 description 3
239000000853 adhesive Substances 0.000 description 3
230000001070 adhesive effect Effects 0.000 description 3
150000003863 ammonium salts Chemical class 0.000 description 3
239000002585 base Substances 0.000 description 3
239000003054 catalyst Substances 0.000 description 3
239000000460 chlorine Substances 0.000 description 3
229940125904 compound 1 Drugs 0.000 description 3
238000010410 dusting Methods 0.000 description 3
239000008187 granular material Substances 0.000 description 3
229910052500 inorganic mineral Inorganic materials 0.000 description 3
239000011707 mineral Substances 0.000 description 3
IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 3
238000002360 preparation method Methods 0.000 description 3
239000011541 reaction mixture Substances 0.000 description 3
239000000377 silicon dioxide Substances 0.000 description 3
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
235000007688 Lycopersicon esculentum Nutrition 0.000 description 2
241000208125 Nicotiana Species 0.000 description 2
OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
241000582441 Peronospora tabacina Species 0.000 description 2
WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 2
150000001298 alcohols Chemical class 0.000 description 2
125000003342 alkenyl group Chemical group 0.000 description 2
229910021529 ammonia Inorganic materials 0.000 description 2
229940124339 anthelmintic agent Drugs 0.000 description 2
239000000921 anthelmintic agent Substances 0.000 description 2
230000000844 anti-bacterial effect Effects 0.000 description 2
229940121375 antifungal agent Drugs 0.000 description 2
239000007900 aqueous suspension Substances 0.000 description 2
239000003899 bactericide agent Substances 0.000 description 2
125000003785 benzimidazolyl group Chemical group N1=C(NC2=C1C=CC=C2)* 0.000 description 2
238000009835 boiling Methods 0.000 description 2
239000003795 chemical substances by application Substances 0.000 description 2
229910052801 chlorine Inorganic materials 0.000 description 2
230000007797 corrosion Effects 0.000 description 2
238000005260 corrosion Methods 0.000 description 2
239000002270 dispersing agent Substances 0.000 description 2
239000006185 dispersion Substances 0.000 description 2
239000000975 dye Substances 0.000 description 2
239000003995 emulsifying agent Substances 0.000 description 2
239000000417 fungicide Substances 0.000 description 2
239000004009 herbicide Substances 0.000 description 2
239000003112 inhibitor Substances 0.000 description 2
230000002401 inhibitory effect Effects 0.000 description 2
230000005764 inhibitory process Effects 0.000 description 2
239000003444 phase transfer catalyst Substances 0.000 description 2
150000002989 phenols Chemical class 0.000 description 2
239000003880 polar aprotic solvent Substances 0.000 description 2
BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
125000001453 quaternary ammonium group Chemical group 0.000 description 2
239000012429 reaction media Substances 0.000 description 2
239000011734 sodium Substances 0.000 description 2
229910052708 sodium Inorganic materials 0.000 description 2
HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Inorganic materials [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 2
239000004550 soluble concentrate Substances 0.000 description 2
238000005507 spraying Methods 0.000 description 2
238000004544 sputter deposition Methods 0.000 description 2
239000000454 talc Substances 0.000 description 2
229910052623 talc Inorganic materials 0.000 description 2
238000012360 testing method Methods 0.000 description 2
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 2
239000000080 wetting agent Substances 0.000 description 2
JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical compound OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 description 1
ZORQXIQZAOLNGE-UHFFFAOYSA-N 1,1-difluorocyclohexane Chemical compound FC1(F)CCCCC1 ZORQXIQZAOLNGE-UHFFFAOYSA-N 0.000 description 1
CPEONABTMRSIKA-UHFFFAOYSA-N 1,4$l^{2}-oxazinane Chemical compound C1COCC[N]1 CPEONABTMRSIKA-UHFFFAOYSA-N 0.000 description 1
MDOGMOWHGBWSHT-UHFFFAOYSA-N 1-hydroxybenzimidazole-2-carbonitrile Chemical compound C1=CC=C2N(O)C(C#N)=NC2=C1 MDOGMOWHGBWSHT-UHFFFAOYSA-N 0.000 description 1
HYZJCKYKOHLVJF-UHFFFAOYSA-N 1H-benzimidazole Chemical compound C1=CC=C2NC=NC2=C1 HYZJCKYKOHLVJF-UHFFFAOYSA-N 0.000 description 1
FMIMHDSOWOYCFO-UHFFFAOYSA-N 2-amino-2-(2-nitrophenyl)acetonitrile Chemical compound N#CC(N)C1=CC=CC=C1[N+]([O-])=O FMIMHDSOWOYCFO-UHFFFAOYSA-N 0.000 description 1
DPJCXCZTLWNFOH-UHFFFAOYSA-N 2-nitroaniline Chemical compound NC1=CC=CC=C1[N+]([O-])=O DPJCXCZTLWNFOH-UHFFFAOYSA-N 0.000 description 1
241000221198 Basidiomycota Species 0.000 description 1
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
239000001692 EU approved anti-caking agent Substances 0.000 description 1
238000004566 IR spectroscopy Methods 0.000 description 1
206010061217 Infestation Diseases 0.000 description 1
FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 1
JGYPHAQVSRTBJA-UHFFFAOYSA-N N-(1H-benzimidazol-2-ylmethylidene)hydroxylamine Chemical compound C1=CC=C2NC(C=NO)=NC2=C1 JGYPHAQVSRTBJA-UHFFFAOYSA-N 0.000 description 1
SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 1
229910004013 NO 2 Inorganic materials 0.000 description 1
244000061176 Nicotiana tabacum Species 0.000 description 1
241000233614 Phytophthora Species 0.000 description 1
229920002125 Sokalan® Polymers 0.000 description 1
240000003768 Solanum lycopersicum Species 0.000 description 1
235000002560 Solanum lycopersicum Nutrition 0.000 description 1
GHVZOJONCUEWAV-UHFFFAOYSA-N [K].CCO Chemical compound [K].CCO GHVZOJONCUEWAV-UHFFFAOYSA-N 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
239000013543 active substance Substances 0.000 description 1
239000000443 aerosol Substances 0.000 description 1
238000005054 agglomeration Methods 0.000 description 1
230000002776 aggregation Effects 0.000 description 1
229910000288 alkali metal carbonate Inorganic materials 0.000 description 1
150000008041 alkali metal carbonates Chemical class 0.000 description 1
229910052784 alkaline earth metal Inorganic materials 0.000 description 1
125000004183 alkoxy alkyl group Chemical group 0.000 description 1
125000004453 alkoxycarbonyl group Chemical group 0.000 description 1
150000001412 amines Chemical class 0.000 description 1
125000002431 aminoalkoxy group Chemical group 0.000 description 1
125000004103 aminoalkyl group Chemical group 0.000 description 1
230000000507 anthelmentic effect Effects 0.000 description 1
239000012871 anti-fungal composition Substances 0.000 description 1
229940124536 anticoccidial agent Drugs 0.000 description 1
239000002518 antifoaming agent Substances 0.000 description 1
239000003429 antifungal agent Substances 0.000 description 1
239000004599 antimicrobial Substances 0.000 description 1
239000007864 aqueous solution Substances 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
239000012298 atmosphere Substances 0.000 description 1
239000011230 binding agent Substances 0.000 description 1
230000003115 biocidal effect Effects 0.000 description 1
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
229910052794 bromium Inorganic materials 0.000 description 1
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
125000001309 chloro group Chemical group Cl* 0.000 description 1
239000003224 coccidiostatic agent Substances 0.000 description 1
239000012141 concentrate Substances 0.000 description 1
238000007796 conventional method Methods 0.000 description 1
239000006184 cosolvent Substances 0.000 description 1
230000006378 damage Effects 0.000 description 1
239000012024 dehydrating agents‎ Substances 0.000 description 1
238000011161 development Methods 0.000 description 1
235000014113 dietary fatty acids Nutrition 0.000 description 1
238000007865 diluting Methods 0.000 description 1
239000003085 diluting agent Substances 0.000 description 1
238000010790 dilution Methods 0.000 description 1
239000012895 dilution Substances 0.000 description 1
238000001035 drying Methods 0.000 description 1
230000001804 emulsifying effect Effects 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 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
239000003337 fertilizer Substances 0.000 description 1
238000001914 filtration Methods 0.000 description 1
239000012530 fluid Substances 0.000 description 1
230000000855 fungicidal effect Effects 0.000 description 1
239000007789 gas Substances 0.000 description 1
229910052736 halogen Inorganic materials 0.000 description 1
150000002367 halogens Chemical class 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
125000005842 heteroatom Chemical group 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
150000002430 hydrocarbons Chemical class 0.000 description 1
229910052739 hydrogen Inorganic materials 0.000 description 1
239000001257 hydrogen Substances 0.000 description 1
125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
238000005470 impregnation Methods 0.000 description 1
238000011065 in-situ storage Methods 0.000 description 1
208000015181 infectious disease Diseases 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
239000002917 insecticide Substances 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
239000000463 material Substances 0.000 description 1
239000008268 mayonnaise Substances 0.000 description 1
235000010746 mayonnaise Nutrition 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
238000002156 mixing Methods 0.000 description 1
239000003607 modifier Substances 0.000 description 1
JFCHSQDLLFJHOA-UHFFFAOYSA-N n,n-dimethylsulfamoyl chloride Chemical compound CN(C)S(Cl)(=O)=O JFCHSQDLLFJHOA-UHFFFAOYSA-N 0.000 description 1
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 1
SNICXCGAKADSCV-UHFFFAOYSA-N nicotine Chemical compound CN1CCCC1C1=CC=CN=C1 SNICXCGAKADSCV-UHFFFAOYSA-N 0.000 description 1
150000002829 nitrogen Chemical class 0.000 description 1
230000000149 penetrating effect Effects 0.000 description 1
239000003208 petroleum Substances 0.000 description 1
RLOWWWKZYUNIDI-UHFFFAOYSA-N phosphinic chloride Chemical compound ClP=O RLOWWWKZYUNIDI-UHFFFAOYSA-N 0.000 description 1
150000003014 phosphoric acid esters Chemical class 0.000 description 1
FAIAAWCVCHQXDN-UHFFFAOYSA-N phosphorus trichloride Chemical compound ClP(Cl)Cl FAIAAWCVCHQXDN-UHFFFAOYSA-N 0.000 description 1
239000004584 polyacrylic acid Substances 0.000 description 1
229910000027 potassium carbonate Inorganic materials 0.000 description 1
230000002265 prevention Effects 0.000 description 1
238000001953 recrystallisation Methods 0.000 description 1
238000010992 reflux Methods 0.000 description 1
239000011347 resin Substances 0.000 description 1
229920005989 resin Polymers 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
238000004062 sedimentation Methods 0.000 description 1
150000004760 silicates Chemical class 0.000 description 1
239000002689 soil Substances 0.000 description 1
239000008247 solid mixture Substances 0.000 description 1
239000001593 sorbitan monooleate Substances 0.000 description 1
229940035049 sorbitan monooleate Drugs 0.000 description 1
235000011069 sorbitan monooleate Nutrition 0.000 description 1
238000004611 spectroscopical analysis Methods 0.000 description 1
239000000126 substance Substances 0.000 description 1
150000003459 sulfonic acid esters Chemical class 0.000 description 1
229920002994 synthetic fiber Polymers 0.000 description 1
230000009897 systematic effect Effects 0.000 description 1
XOAAWQZATWQOTB-UHFFFAOYSA-N taurine Chemical class NCCS(O)(=O)=O XOAAWQZATWQOTB-UHFFFAOYSA-N 0.000 description 1
239000013008 thixotropic agent Substances 0.000 description 1
125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 description 1
239000001993 wax Substances 0.000 description 1
239000004563 wettable powder Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
- C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
- C07D235/24—Benzimidazoles; Hydrogenated benzimidazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached in position 2

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Plural Heterocyclic Compounds (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

DD85282073A 1984-10-26 1985-10-25 Pestizide zusammensetzung DD240494A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
FR8416620A FR2572401B1 (fr)	1984-10-26	1984-10-26	Nouveaux derives du cyano-2 benzimidazole, leur preparation et leur utilisation comme fongicides et acaricides

Publications (1)

Publication Number	Publication Date
DD240494A5 true DD240494A5 (de)	1986-11-05

Family

ID=9309160

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD85282073A DD240494A5 (de)	1984-10-26	1985-10-25	Pestizide zusammensetzung

Country Status (14)

Country	Link
EP (1)	EP0181826A1 (da)
JP (1)	JPS61103873A (da)
KR (1)	KR860003231A (da)
CN (1)	CN85107900A (da)
AU (1)	AU4901285A (da)
BR (1)	BR8505334A (da)
DD (1)	DD240494A5 (da)
DK (1)	DK490185A (da)
ES (1)	ES8609273A1 (da)
FR (1)	FR2572401B1 (da)
HU (1)	HUT39327A (da)
IL (1)	IL76685A0 (da)
PT (1)	PT81377B (da)
ZA (1)	ZA858185B (da)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
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
AU638614B2 (en) *	1990-11-20	1993-07-01	Sumitomo Chemical Company, Limited	Benzimidazole derivative, a method for producing the same, its intermediate compounds and an agricultural and horticultural fungicide containing the benzimidazole derivative as an active ingredient
CA2085311A1 (en) *	1991-12-16	1993-06-17	Adolf Hubele	Microbicides
DE4237597A1 (de) *	1992-11-06	1994-05-11	Bayer Ag	Substituierte Benzimidazole
US5376657A (en) *	1992-12-10	1994-12-27	Ciba-Geigy Corporation	Microbicides
DE19920551A1 (de)	1999-05-05	2000-11-09	Bayer Ag	Substituierte Benzimidazole, ihre Herstellung und ihre Verwendung als Mittel gegen parasitäre Protozoen
DE102009038950A1 (de)	2009-08-26	2011-03-03	Bayer Animal Health Gmbh	Neue antiparasitäre Kombination von Wirkstoffen

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
FR2521141A1 (fr) *	1982-02-09	1983-08-12	Rhone Poulenc Agrochimie	Nouveaux derives du cyano-2 benzimidazole, leur preparation et leur utilisation comme fongicides
FR2559150B1 (fr) *	1984-02-06	1986-06-27	Rhone Poulenc Agrochimie	Nouveaux derives du cyano-2 benzimidazole, leur preparation et leur utilisation comme fongicides

1984
- 1984-10-26 FR FR8416620A patent/FR2572401B1/fr not_active Expired
1985
- 1985-10-04 ES ES547599A patent/ES8609273A1/es not_active Expired
- 1985-10-13 IL IL76685A patent/IL76685A0/xx unknown
- 1985-10-24 EP EP85420193A patent/EP0181826A1/fr not_active Withdrawn
- 1985-10-24 AU AU49012/85A patent/AU4901285A/en not_active Abandoned
- 1985-10-24 ZA ZA858185A patent/ZA858185B/xx unknown
- 1985-10-25 HU HU854122A patent/HUT39327A/hu unknown
- 1985-10-25 JP JP60239237A patent/JPS61103873A/ja active Pending
- 1985-10-25 DK DK490185A patent/DK490185A/da not_active Application Discontinuation
- 1985-10-25 PT PT81377A patent/PT81377B/pt unknown
- 1985-10-25 BR BR8505334A patent/BR8505334A/pt unknown
- 1985-10-25 KR KR1019850007914A patent/KR860003231A/ko not_active Withdrawn
- 1985-10-25 DD DD85282073A patent/DD240494A5/de unknown
- 1985-10-26 CN CN198585107900A patent/CN85107900A/zh active Pending

Also Published As

Publication number	Publication date
KR860003231A (ko)	1986-05-21
FR2572401A1 (fr)	1986-05-02
DK490185A (da)	1986-04-27
FR2572401B1 (fr)	1986-12-26
ES547599A0 (es)	1986-09-01
CN85107900A (zh)	1986-06-10
ZA858185B (en)	1986-06-25
HUT39327A (en)	1986-09-29
EP0181826A1 (fr)	1986-05-21
IL76685A0 (en)	1986-02-28
DK490185D0 (da)	1985-10-25
ES8609273A1 (es)	1986-09-01
JPS61103873A (ja)	1986-05-22
PT81377A (fr)	1985-11-01
BR8505334A (pt)	1986-08-05
PT81377B (fr)	1987-08-20
AU4901285A (en)	1986-05-01

Publication	Publication Date	Title
EP0083556B1 (de)	1986-08-20	Alpha-(4-(3'-Fluor-5'-halogen-pyridyl-2'-oxy)-phenoxy)-propionsäure derivate mit herbizider Wirkung
DE68923601T2 (de)	1996-03-28	Nitromethylenverbindungen, deren Herstellung und deren Verwendung als Pestizide.
DD208753A5 (de)	1984-04-11	Pestizide zusammensetzungen zur verwendung in der landwirtschaft
DD157071A5 (de)	1982-10-13	Aphicide zusammensetzung
EP0007990A1 (de)	1980-02-20	Pyrazolätherderivate, Verfahren zu ihrer Herstellung und Herbizide, die diese Verbindungen enthalten
DD232184A5 (de)	1986-01-22	Pestizide zusammensetzung
DE2331398A1 (de)	1975-01-23	Phenylpyridazine, ihre herstellung und verwendung als herbizide
DE1274401B (de)	1968-08-01	Herbicides Mittel
DE3514116A1 (de)	1986-10-23	Neue cyclohexyl- und cyclohexenylimidazolverbindungen, verfahren zu ihrer herstellung und ihre verwendung als pflanzenwachstumsregulatoren
DD240494A5 (de)	1986-11-05	Pestizide zusammensetzung
DD149452A5 (de)	1981-07-15	Fungizide zusammensetzung
EP0024259B1 (de)	1985-07-31	Derivate der 5-(Pyridyl-2-oxy)-2-nitrobenzoesäure, deren Herstellung und sie enthaltende herbizide Mittel
DE3227869A1 (de)	1983-03-24	Herbizide phenoxybenzoesaeureverbindungen
EP0183993A2 (de)	1986-06-11	2H-Imidazo[1',2':1,2]pyrrolo[3,4-b]pyridine und deren Verwendung als Unkrautbekämpfungsmittel
DD145222A5 (de)	1980-12-03	Pestizide und/oder wachstumsregulierende zusammensetzungen
DE69106252T2 (de)	1995-05-18	Herbizide Zusammensetzung.
DD234603A5 (de)	1986-04-09	Antifungische zusammensetzung
DD223906A5 (de)	1985-06-26	Pesticide zusammensetzungen zur bekaempfung phytopathogener pilze
DE3110473C2 (de)	1986-02-13	N-Alkyl-2'-n-butoxy-6'-ethyl-2-chloracetanilide und Herbizide, welche diese Verbindungen enthalten
DD262992A5 (de)	1988-12-21	Nematizide und insektizide zusammensetzung
DD215002A5 (de)	1984-10-31	Pestizide zusammensetzung
DE2260763C3 (de)	1979-11-29	Bekämpfung von schädlichen Organismen mit Dihalogenpropansulfonsäureesterderivaten
DD202372A5 (de)	1983-09-14	Herbizides mittel
DD273252A5 (de)	1989-11-08	Verfahren zur herstellung von imidazolderivaten und diese derivate enthaltende fungizide zusammensetzung
DE2854603A1 (de)	1979-07-05	Neue pyrazinderivate, verfahren zu deren herstellung und deren anwendung