PL150666B1 - A weed killer ans a fungicide - Google Patents

A weed killer ans a fungicide

Info

Publication number: PL150666B1
Authority: PL; Poland
Prior art keywords: pattern; ppm; tms; formula; weight
Prior art date: 1984-08-10

Application number

PL26786385A

Other languages

English (en)

Polish (pl)

Other versions

PL267863A1 (en

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.)

1984-08-10

Filing date

1985-08-09

Publication date

1990-06-30

1985-08-09 Application filed filed Critical

1988-06-09 Publication of PL267863A1 publication Critical patent/PL267863A1/xx

1990-06-30 Publication of PL150666B1 publication Critical patent/PL150666B1/pl

Links

239000004009 herbicide Substances 0.000 title claims description 18
239000000417 fungicide Substances 0.000 title claims description 14
230000000855 fungicidal effect Effects 0.000 title claims description 9
YZHUMGUJCQRKBT-UHFFFAOYSA-M sodium chlorate Chemical compound [Na+].[O-]Cl(=O)=O YZHUMGUJCQRKBT-UHFFFAOYSA-M 0.000 title 1
239000004480 active ingredient Substances 0.000 claims description 15
230000002363 herbicidal effect Effects 0.000 claims description 15
-1 methylenedioxy group Chemical group 0.000 claims description 13
YWAQAPAIGNRNSJ-UHFFFAOYSA-N 2-prop-2-ynoxyacetonitrile Chemical class C#CCOCC#N YWAQAPAIGNRNSJ-UHFFFAOYSA-N 0.000 claims description 7
125000000217 alkyl group Chemical group 0.000 claims description 6
239000007787 solid Substances 0.000 claims description 6
125000005843 halogen group Chemical group 0.000 claims description 5
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 5
239000007788 liquid Substances 0.000 claims description 5
239000003085 diluting agent Substances 0.000 claims description 3
125000001188 haloalkyl group Chemical group 0.000 claims description 3
229910052739 hydrogen Inorganic materials 0.000 claims description 3
239000001257 hydrogen Substances 0.000 claims description 3
239000004094 surface-active agent Substances 0.000 claims description 3
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
125000003545 alkoxy group Chemical group 0.000 claims description 2
125000004093 cyano group Chemical group *C#N 0.000 claims description 2
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 2
150000002431 hydrogen Chemical class 0.000 claims 1
238000012360 testing method Methods 0.000 description 44
241000196324 Embryophyta Species 0.000 description 42
150000001875 compounds Chemical class 0.000 description 42
239000000203 mixture Substances 0.000 description 28
239000003795 chemical substances by application Substances 0.000 description 24
201000010099 disease Diseases 0.000 description 22
208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 22
240000007594 Oryza sativa Species 0.000 description 19
235000007164 Oryza sativa Nutrition 0.000 description 19
235000009566 rice Nutrition 0.000 description 19
239000000126 substance Substances 0.000 description 14
231100000674 Phytotoxicity Toxicity 0.000 description 12
240000008067 Cucumis sativus Species 0.000 description 9
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 9
230000000694 effects Effects 0.000 description 9
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
239000004563 wettable powder Substances 0.000 description 9
244000061456 Solanum tuberosum Species 0.000 description 8
235000002595 Solanum tuberosum Nutrition 0.000 description 7
239000000428 dust Substances 0.000 description 7
239000008187 granular material Substances 0.000 description 7
239000002689 soil Substances 0.000 description 7
239000000725 suspension Substances 0.000 description 7
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 6
OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 6
238000000034 method Methods 0.000 description 6
238000002360 preparation method Methods 0.000 description 6
235000010799 Cucumis sativus var sativus Nutrition 0.000 description 5
206010017711 Gangrene Diseases 0.000 description 5
239000012298 atmosphere Substances 0.000 description 5
238000003898 horticulture Methods 0.000 description 5
WEVYAHXRMPXWCK-UHFFFAOYSA-N methyl cyanide Natural products CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 5
VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 4
239000005909 Kieselgur Substances 0.000 description 4
241000233679 Peronosporaceae Species 0.000 description 4
230000012010 growth Effects 0.000 description 4
239000000454 talc Substances 0.000 description 4
229910052623 talc Inorganic materials 0.000 description 4
235000012222 talc Nutrition 0.000 description 4
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
241000219310 Beta vulgaris subsp. vulgaris Species 0.000 description 3
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 3
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-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
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
240000000178 Monochoria vaginalis Species 0.000 description 3
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
235000011999 Panicum crusgalli Nutrition 0.000 description 3
235000021536 Sugar beet Nutrition 0.000 description 3
QHTQREMOGMZHJV-UHFFFAOYSA-N Thiobencarb Chemical compound CCN(CC)C(=O)SCC1=CC=C(Cl)C=C1 QHTQREMOGMZHJV-UHFFFAOYSA-N 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
238000007605 air drying Methods 0.000 description 3
230000004071 biological effect Effects 0.000 description 3
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 3
229910052794 bromium Inorganic materials 0.000 description 3
HKPHPIREJKHECO-UHFFFAOYSA-N butachlor Chemical compound CCCCOCN(C(=O)CCl)C1=C(CC)C=CC=C1CC HKPHPIREJKHECO-UHFFFAOYSA-N 0.000 description 3
239000001175 calcium sulphate Substances 0.000 description 3
235000011132 calcium sulphate Nutrition 0.000 description 3
244000038559 crop plants Species 0.000 description 3
239000004495 emulsifiable concentrate Substances 0.000 description 3
238000009472 formulation Methods 0.000 description 3
KGVPNLBXJKTABS-UHFFFAOYSA-N hymexazol Chemical compound CC1=CC(O)=NO1 KGVPNLBXJKTABS-UHFFFAOYSA-N 0.000 description 3
230000000885 phytotoxic effect Effects 0.000 description 3
239000011734 sodium Substances 0.000 description 3
229910052708 sodium Inorganic materials 0.000 description 3
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
241000251468 Actinopterygii Species 0.000 description 2
241000748223 Alisma Species 0.000 description 2
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 2
OYPRJOBELJOOCE-RKEGKUSMSA-N Calcium-47 Chemical group [47Ca] OYPRJOBELJOOCE-RKEGKUSMSA-N 0.000 description 2
229920002134 Carboxymethyl cellulose Polymers 0.000 description 2
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
235000009849 Cucumis sativus Nutrition 0.000 description 2
241000234653 Cyperus Species 0.000 description 2
244000108484 Cyperus difformis Species 0.000 description 2
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
244000058871 Echinochloa crus-galli Species 0.000 description 2
241000064140 Lindernia Species 0.000 description 2
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
241000233614 Phytophthora Species 0.000 description 2
241001281802 Pseudoperonospora Species 0.000 description 2
244000155504 Rotala indica Species 0.000 description 2
244000085269 Scirpus juncoides Species 0.000 description 2
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
241001148683 Zostera marina Species 0.000 description 2
150000007960 acetonitrile Chemical class 0.000 description 2
230000015572 biosynthetic process Effects 0.000 description 2
229910000019 calcium carbonate Inorganic materials 0.000 description 2
239000001768 carboxy methyl cellulose Substances 0.000 description 2
235000010948 carboxy methyl cellulose Nutrition 0.000 description 2
239000008112 carboxymethyl-cellulose Substances 0.000 description 2
239000000969 carrier Substances 0.000 description 2
238000006243 chemical reaction Methods 0.000 description 2
CRQQGFGUEAVUIL-UHFFFAOYSA-N chlorothalonil Chemical compound ClC1=C(Cl)C(C#N)=C(Cl)C(C#N)=C1Cl CRQQGFGUEAVUIL-UHFFFAOYSA-N 0.000 description 2
239000004927 clay Substances 0.000 description 2
RWGFKTVRMDUZSP-UHFFFAOYSA-N cumene Chemical compound CC(C)C1=CC=CC=C1 RWGFKTVRMDUZSP-UHFFFAOYSA-N 0.000 description 2
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
238000011161 development Methods 0.000 description 2
238000010410 dusting Methods 0.000 description 2
235000013312 flour Nutrition 0.000 description 2
230000002538 fungal effect Effects 0.000 description 2
231100000053 low toxicity Toxicity 0.000 description 2
BCTQJXQXJVLSIG-UHFFFAOYSA-N mepronil Chemical compound CC(C)OC1=CC=CC(NC(=O)C=2C(=CC=CC=2)C)=C1 BCTQJXQXJVLSIG-UHFFFAOYSA-N 0.000 description 2
AYISBGOOBSNECJ-UHFFFAOYSA-N n-[but-2-ynoxy(cyano)methyl]-3,5-dichlorobenzamide Chemical compound CC#CCOC(C#N)NC(=O)C1=CC(Cl)=CC(Cl)=C1 AYISBGOOBSNECJ-UHFFFAOYSA-N 0.000 description 2
231100000915 pathological change Toxicity 0.000 description 2
230000036285 pathological change Effects 0.000 description 2
239000000546 pharmaceutical excipient Substances 0.000 description 2
235000012015 potatoes Nutrition 0.000 description 2
230000003449 preventive effect Effects 0.000 description 2
230000001681 protective effect Effects 0.000 description 2
238000011160 research Methods 0.000 description 2
229920005552 sodium lignosulfonate Polymers 0.000 description 2
239000007921 spray Substances 0.000 description 2
238000005507 spraying Methods 0.000 description 2
VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
238000009736 wetting Methods 0.000 description 2
239000008096 xylene Substances 0.000 description 2
ZQEIXNIJLIKNTD-LBPRGKRZSA-N (S)-metalaxyl Chemical compound COCC(=O)N([C@@H](C)C(=O)OC)C1=C(C)C=CC=C1C ZQEIXNIJLIKNTD-LBPRGKRZSA-N 0.000 description 1
SCYULBFZEHDVBN-UHFFFAOYSA-N 1,1-Dichloroethane Chemical compound CC(Cl)Cl SCYULBFZEHDVBN-UHFFFAOYSA-N 0.000 description 1
RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 description 1
JUUOPULAHBFBFP-UHFFFAOYSA-N 2-amino-3-(3,5-dichlorophenyl)-3-oxopropanenitrile Chemical compound N#CC(N)C(=O)C1=CC(Cl)=CC(Cl)=C1 JUUOPULAHBFBFP-UHFFFAOYSA-N 0.000 description 1
UENGBOCGGKLVJJ-UHFFFAOYSA-N 2-chloro-1-(2,4-difluorophenyl)ethanone Chemical compound FC1=CC=C(C(=O)CCl)C(F)=C1 UENGBOCGGKLVJJ-UHFFFAOYSA-N 0.000 description 1
244000215068 Acacia senegal Species 0.000 description 1
241000172143 Aphanomyces cochlioides Species 0.000 description 1
SLCGUGMPSUYJAY-UHFFFAOYSA-N Benzoylprop-ethyl Chemical class C=1C=C(Cl)C(Cl)=CC=1N(C(C)C(=O)OCC)C(=O)C1=CC=CC=C1 SLCGUGMPSUYJAY-UHFFFAOYSA-N 0.000 description 1
235000016068 Berberis vulgaris Nutrition 0.000 description 1
241000335053 Beta vulgaris Species 0.000 description 1
IAZDPXIOMUYVGZ-WFGJKAKNSA-N DMSO-d6 Substances [2H]C([2H])([2H])S(=O)C([2H])([2H])[2H] IAZDPXIOMUYVGZ-WFGJKAKNSA-N 0.000 description 1
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
239000005977 Ethylene Substances 0.000 description 1
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244000088461 Panicum crus-galli Species 0.000 description 1
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240000003768 Solanum lycopersicum Species 0.000 description 1
235000021307 Triticum Nutrition 0.000 description 1
244000098338 Triticum aestivum Species 0.000 description 1
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
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HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
239000000205 acacia gum Substances 0.000 description 1
235000010489 acacia gum Nutrition 0.000 description 1
239000003905 agrochemical Substances 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
150000001408 amides Chemical class 0.000 description 1
DFNYGALUNNFWKJ-UHFFFAOYSA-N aminoacetonitrile Chemical compound NCC#N DFNYGALUNNFWKJ-UHFFFAOYSA-N 0.000 description 1
BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 1
229910052921 ammonium sulfate Inorganic materials 0.000 description 1
239000001166 ammonium sulphate Substances 0.000 description 1
235000011130 ammonium sulphate Nutrition 0.000 description 1
150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
JXLHNMVSKXFWAO-UHFFFAOYSA-N azane;7-fluoro-2,1,3-benzoxadiazole-4-sulfonic acid Chemical compound N.OS(=O)(=O)C1=CC=C(F)C2=NON=C12 JXLHNMVSKXFWAO-UHFFFAOYSA-N 0.000 description 1
239000000440 bentonite Substances 0.000 description 1
229910000278 bentonite Inorganic materials 0.000 description 1
SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
150000003936 benzamides Chemical class 0.000 description 1
238000009739 binding Methods 0.000 description 1
CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 1
239000008116 calcium stearate Substances 0.000 description 1
235000013539 calcium stearate Nutrition 0.000 description 1
OOCMUZJPDXYRFD-UHFFFAOYSA-L calcium;2-dodecylbenzenesulfonate Chemical compound [Ca+2].CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O.CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O OOCMUZJPDXYRFD-UHFFFAOYSA-L 0.000 description 1
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239000011248 coating agent Substances 0.000 description 1
238000000576 coating method Methods 0.000 description 1
230000000052 comparative effect Effects 0.000 description 1
238000001816 cooling Methods 0.000 description 1
230000001419 dependent effect Effects 0.000 description 1
238000010586 diagram Methods 0.000 description 1
GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical compound O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 description 1
235000019329 dioctyl sodium sulphosuccinate Nutrition 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
230000002554 disease preventive effect Effects 0.000 description 1
YHAIUSTWZPMYGG-UHFFFAOYSA-L disodium;2,2-dioctyl-3-sulfobutanedioate Chemical compound [Na+].[Na+].CCCCCCCCC(C([O-])=O)(C(C([O-])=O)S(O)(=O)=O)CCCCCCCC YHAIUSTWZPMYGG-UHFFFAOYSA-L 0.000 description 1
YVIGPQSYEAOLAD-UHFFFAOYSA-L disodium;dodecyl phosphate Chemical compound [Na+].[Na+].CCCCCCCCCCCCOP([O-])([O-])=O YVIGPQSYEAOLAD-UHFFFAOYSA-L 0.000 description 1
239000012990 dithiocarbamate Substances 0.000 description 1
230000001804 emulsifying effect Effects 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
239000003337 fertilizer Substances 0.000 description 1
244000000004 fungal plant pathogen Species 0.000 description 1
239000010440 gypsum Substances 0.000 description 1
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150000008282 halocarbons Chemical class 0.000 description 1
230000002140 halogenating effect Effects 0.000 description 1
230000035876 healing Effects 0.000 description 1
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150000002430 hydrocarbons Chemical class 0.000 description 1
238000010348 incorporation Methods 0.000 description 1
208000015181 infectious disease Diseases 0.000 description 1
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239000002917 insecticide Substances 0.000 description 1
QPPQHRDVPBTVEV-UHFFFAOYSA-N isopropyl dihydrogen phosphate Chemical compound CC(C)OP(O)(O)=O QPPQHRDVPBTVEV-UHFFFAOYSA-N 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
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239000003350 kerosene Substances 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
230000002147 killing effect Effects 0.000 description 1
230000003902 lesion Effects 0.000 description 1
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ZQEIXNIJLIKNTD-UHFFFAOYSA-N methyl N-(2,6-dimethylphenyl)-N-(methoxyacetyl)alaninate Chemical compound COCC(=O)N(C(C)C(=O)OC)C1=C(C)C=CC=C1C ZQEIXNIJLIKNTD-UHFFFAOYSA-N 0.000 description 1
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PSZYNBSKGUBXEH-UHFFFAOYSA-M naphthalene-1-sulfonate Chemical compound C1=CC=C2C(S(=O)(=O)[O-])=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-M 0.000 description 1
PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical compound C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
239000002736 nonionic surfactant Substances 0.000 description 1
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TVDSBUOJIPERQY-UHFFFAOYSA-N prop-2-yn-1-ol Chemical class OCC#C TVDSBUOJIPERQY-UHFFFAOYSA-N 0.000 description 1
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239000011541 reaction mixture Substances 0.000 description 1
230000002829 reductive effect Effects 0.000 description 1
239000000741 silica gel Substances 0.000 description 1
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239000002904 solvent Substances 0.000 description 1
238000009331 sowing Methods 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
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150000003871 sulfonates Chemical class 0.000 description 1
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YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
230000001225 therapeutic effect Effects 0.000 description 1
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230000001988 toxicity Effects 0.000 description 1
NRTLTGGGUQIRRT-UHFFFAOYSA-N triethylazanium;bromide Chemical compound [Br-].CC[NH+](CC)CC NRTLTGGGUQIRRT-UHFFFAOYSA-N 0.000 description 1
235000013311 vegetables Nutrition 0.000 description 1
239000010455 vermiculite Substances 0.000 description 1
229910052902 vermiculite Inorganic materials 0.000 description 1
235000019354 vermiculite Nutrition 0.000 description 1
239000001993 wax Substances 0.000 description 1
239000011701 zinc Substances 0.000 description 1
229910052725 zinc Inorganic materials 0.000 description 1
AMHNZOICSMBGDH-UHFFFAOYSA-L zineb Chemical compound [Zn+2].[S-]C(=S)NCCNC([S-])=S AMHNZOICSMBGDH-UHFFFAOYSA-L 0.000 description 1

Landscapes

Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)

PL26786385A 1984-08-10 1985-08-09 A weed killer ans a fungicide PL150666B1 (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP16631684A JPS6144857A (ja)	1984-08-10	1984-08-10	置換プロパルギルオキシアセニトリル誘導体、その製造法およびそれらを有効成分とする除草剤および農園芸用殺菌剤

Publications (2)

Publication Number	Publication Date
PL267863A1 PL267863A1 (en)	1988-06-09
PL150666B1 true PL150666B1 (en)	1990-06-30

Family

ID=15829088

Family Applications (2)

Application Number	Title	Priority Date	Filing Date
PL26786385A PL150666B1 (en)	1984-08-10	1985-08-09	A weed killer ans a fungicide
PL25493185A PL147819B1 (en)	1984-08-10	1985-08-09	Method of obtaining novel derivatives of propargiloksyacetnitrile

Family Applications After (1)

Application Number	Title	Priority Date	Filing Date
PL25493185A PL147819B1 (en)	1984-08-10	1985-08-09	Method of obtaining novel derivatives of propargiloksyacetnitrile

Country Status (3)

Country	Link
JP (1)	JPS6144857A (de)
DD (2)	DD251125A5 (de)
PL (2)	PL150666B1 (de)

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB8401410D0 (en) *	1984-01-19	1984-02-22	Ici Plc	Biologically active amide derivatives
JPS60228451A (ja) *	1984-04-27	1985-11-13	Mitsui Toatsu Chem Inc	ジフエニルエ−テル誘導体およびこれを含有する有害生物防除剤

1984
- 1984-08-10 JP JP16631684A patent/JPS6144857A/ja active Pending
1985
- 1985-08-07 DD DD85279462A patent/DD251125A5/de not_active IP Right Cessation
- 1985-08-07 DD DD31064985A patent/DD281949A5/de not_active IP Right Cessation
- 1985-08-09 PL PL26786385A patent/PL150666B1/pl unknown
- 1985-08-09 PL PL25493185A patent/PL147819B1/pl unknown

Also Published As

Publication number	Publication date
JPS6144857A (ja)	1986-03-04
DD251125A5 (de)	1987-11-04
PL267863A1 (en)	1988-06-09
PL147819B1 (en)	1989-08-31
DD281949A5 (de)	1990-08-29
PL254931A1 (en)	1988-02-04

Publication	Publication Date	Title
EP0171768B1 (de)	1988-11-17	Substituierte Propargyloxyacetonitrilderivate, Verfahren zu ihrer Herstellung sowie diese Derivate als Wirkstoffe enthaltende Herbizide und Fungizide für Landwirtschaft und Gartenbau
PL167500B1 (pl)	1995-09-30	Srodek grzybobójczy PL PL
KR19980018703A (ko)	1998-06-05	치환카르복시산아닐리드유도체 및 이것을 유효성분으로 하는 식물병해방제제(substituted carboxylic acid anilide derivatives and preventive and exterminator of blight comprising the derivative as active ingredinet)
SK280607B6 (sk)	2000-05-16	Amidy n-sulfonyl- a n-sulfinylaminokyselín, spôsob
IL93438A (en)	1994-07-31	Compositions comprising derivatives of n-phenyl-3,4,5,6- tetrahydrophthalimide for use in the desiccation and abscission of plant organs
US4144049A (en)	1979-03-13	N-(4-Benzyloxyphenyl)-N-methyl-N-methoxyurea
JPH06172348A (ja)	1994-06-21	有害生物防除剤
EP0061583B1 (de)	1984-05-02	Alpha-alpha-Dimethyl-phenylacetanilide enthaltende herbizide Zusammensetzungen
PL150666B1 (en)	1990-06-30	A weed killer ans a fungicide
JPH0655705B2 (ja)	1994-07-27	アシルアミノバレロニトリル誘導体、その製造法およびそれらを含有する除草剤および農園芸用殺菌剤
US4758263A (en)	1988-07-19	2-(2,5-difluorophenyl)-4-methyl-1,2,4-oxadiazolidine-3,5 diones
US4685962A (en)	1987-08-11	Phenylacetanilide derivatives
US5795878A (en)	1998-08-18	Biocidal compounds their preparation and use
JPH0559900B2 (de)	1993-09-01
JPS62103056A (ja)	1987-05-13	アシルアミノブテニルニトリル誘導体、その製造法およびそれらを含有する除草剤および農園芸用殺菌剤
JPS62103067A (ja)	1987-05-13	ピラゾ−ル誘導体、それらの製造法およびそれらを含有する除草剤および農園芸用殺菌剤
JPH0643422B2 (ja)	1994-06-08	Ｎ−（α−シアノフルフリル）ニコチン酸アミド誘導体、その製造法およびそれらを含有する除草剤および農園芸用殺菌剤
JPH0267207A (ja)	1990-03-07	農園芸用殺菌剤組成物
JPH0655704B2 (ja)	1994-07-27	アシルアミノプロピオニトリル誘導体、その製造法およびそれらを含有する除草剤および農園芸用殺菌剤
JPS62209056A (ja)	1987-09-14	ベンズアミド誘導体、その製造法およびそれらを含有する除草剤および農園芸用殺菌剤
GB2135301A (en)	1984-08-30	Herbicidal chloroacetanilide derivatives
JPS6115857B2 (de)	1986-04-26
JPS61212553A (ja)	1986-09-20	アシルアミノ誘導体、その製造法およびそれらを含有する除草剤および農園芸用殺菌剤
EP0198687A2 (de)	1986-10-22	Alpha-polyhalogenierte Ketoxime
JPS625949A (ja)	1987-01-12	アシルアミノ誘導体，その製造法およびそれらを含有する除草剤および農園芸用殺菌剤