DD298874A5 - Pflanzenakarizide - Google Patents

Pflanzenakarizide Download PDF

Info

Publication number: DD298874A5
Authority: DD; German Democratic Republic
Prior art keywords: formula; active ingredient; methyl; acid; compound
Prior art date: 1989-08-10

Application number

DD90343330A

Other languages

German (de)

English (en)

Inventor

Marius Sutter

Johannes P Pachlatko

Gerhard Hoefle

Hans Reichenbach

Original Assignee

Ciba-Geigy Ag,Ch

Gesellschaft Fuer Biotechnologische Forschung Mbh,De

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.)

1989-08-10

Filing date

1990-08-08

Publication date

1992-03-19

1990-08-08 Application filed by Ciba-Geigy Ag,Ch, Gesellschaft Fuer Biotechnologische Forschung Mbh,De filed Critical Ciba-Geigy Ag,Ch

1992-03-19 Publication of DD298874A5 publication Critical patent/DD298874A5/de

Links

150000001875 compounds Chemical class 0.000 claims abstract description 28
229910052739 hydrogen Inorganic materials 0.000 claims abstract description 3
239000001257 hydrogen Substances 0.000 claims abstract description 3
125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 3
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 3
239000004480 active ingredient Substances 0.000 claims description 30
-1 Bifenate Chemical compound 0.000 claims description 24
239000000203 mixture Substances 0.000 claims description 18
238000000034 method Methods 0.000 claims description 7
241000607479 Yersinia pestis Species 0.000 claims description 6
230000000895 acaricidal effect Effects 0.000 claims description 6
241000488583 Panonychus ulmi Species 0.000 claims description 5
241000344246 Tetranychus cinnabarinus Species 0.000 claims description 5
241001454293 Tetranychus urticae Species 0.000 claims description 5
241001454295 Tetranychidae Species 0.000 claims description 4
NYPJDWWKZLNGGM-UHFFFAOYSA-N fenvalerate Chemical compound C=1C=C(Cl)C=CC=1C(C(C)C)C(=O)OC(C#N)C(C=1)=CC=CC=1OC1=CC=CC=C1 NYPJDWWKZLNGGM-UHFFFAOYSA-N 0.000 claims description 4
KRTSDMXIXPKRQR-AATRIKPKSA-N monocrotophos Chemical compound CNC(=O)\C=C(/C)OP(=O)(OC)OC KRTSDMXIXPKRQR-AATRIKPKSA-N 0.000 claims description 4
XLNZEKHULJKQBA-UHFFFAOYSA-N terbufos Chemical compound CCOP(=S)(OCC)SCSC(C)(C)C XLNZEKHULJKQBA-UHFFFAOYSA-N 0.000 claims description 4
IAKOZHOLGAGEJT-UHFFFAOYSA-N 1,1,1-trichloro-2,2-bis(p-methoxyphenyl)-Ethane Chemical compound C1=CC(OC)=CC=C1C(C(Cl)(Cl)Cl)C1=CC=C(OC)C=C1 IAKOZHOLGAGEJT-UHFFFAOYSA-N 0.000 claims description 3
239000013543 active substance Substances 0.000 claims description 3
CVXBEEMKQHEXEN-UHFFFAOYSA-N carbaryl Chemical compound C1=CC=C2C(OC(=O)NC)=CC=CC2=C1 CVXBEEMKQHEXEN-UHFFFAOYSA-N 0.000 claims description 3
UOAMTSKGCBMZTC-UHFFFAOYSA-N dicofol Chemical compound C=1C=C(Cl)C=CC=1C(C(Cl)(Cl)Cl)(O)C1=CC=C(Cl)C=C1 UOAMTSKGCBMZTC-UHFFFAOYSA-N 0.000 claims description 3
XAIPTRIXGHTTNT-UHFFFAOYSA-N triflumuron Chemical compound C1=CC(OC(F)(F)F)=CC=C1NC(=O)NC(=O)C1=CC=CC=C1Cl XAIPTRIXGHTTNT-UHFFFAOYSA-N 0.000 claims description 3
XGWIJUOSCAQSSV-XHDPSFHLSA-N (S,S)-hexythiazox Chemical compound S([C@H]([C@@H]1C)C=2C=CC(Cl)=CC=2)C(=O)N1C(=O)NC1CCCCC1 XGWIJUOSCAQSSV-XHDPSFHLSA-N 0.000 claims description 2
YNEKMCSWRMRXIR-UHFFFAOYSA-N 2,3,5,5-tetrachloro-4,7-bis(chloromethyl)-7-(dichloromethyl)bicyclo[2.2.1]heptane Chemical compound C1C(Cl)(Cl)C2(CCl)C(Cl)C(Cl)C1C2(C(Cl)Cl)CCl YNEKMCSWRMRXIR-UHFFFAOYSA-N 0.000 claims description 2
PRLVTUNWOQKEAI-UHFFFAOYSA-N 2-(tert-butylimino)-5-phenyl-3-(propan-2-yl)-1,3,5-thiadiazinan-4-one Chemical compound O=C1N(C(C)C)C(=NC(C)(C)C)SCN1C1=CC=CC=C1 PRLVTUNWOQKEAI-UHFFFAOYSA-N 0.000 claims description 2
ZRDUSMYWDRPZRM-UHFFFAOYSA-N 2-sec-butyl-4,6-dinitrophenyl 3-methylbut-2-enoate Chemical compound CCC(C)C1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1OC(=O)C=C(C)C ZRDUSMYWDRPZRM-UHFFFAOYSA-N 0.000 claims description 2
239000005874 Bifenthrin Substances 0.000 claims description 2
STUSTWKEFDQFFZ-UHFFFAOYSA-N Chlordimeform Chemical compound CN(C)C=NC1=CC=C(Cl)C=C1C STUSTWKEFDQFFZ-UHFFFAOYSA-N 0.000 claims description 2
RAPBNVDSDCTNRC-UHFFFAOYSA-N Chlorobenzilate Chemical compound C=1C=C(Cl)C=CC=1C(O)(C(=O)OCC)C1=CC=C(Cl)C=C1 RAPBNVDSDCTNRC-UHFFFAOYSA-N 0.000 claims description 2
239000005944 Chlorpyrifos Substances 0.000 claims description 2
239000005946 Cypermethrin Substances 0.000 claims description 2
239000005892 Deltamethrin Substances 0.000 claims description 2
LWLJUMBEZJHXHV-UHFFFAOYSA-N Dienochlor Chemical compound ClC1=C(Cl)C(Cl)=C(Cl)C1(Cl)C1(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl LWLJUMBEZJHXHV-UHFFFAOYSA-N 0.000 claims description 2
239000005947 Dimethoate Substances 0.000 claims description 2
AIGRXSNSLVJMEA-UHFFFAOYSA-N EPN Chemical compound C=1C=CC=CC=1P(=S)(OCC)OC1=CC=C([N+]([O-])=O)C=C1 AIGRXSNSLVJMEA-UHFFFAOYSA-N 0.000 claims description 2
239000005661 Hexythiazox Substances 0.000 claims description 2
239000005949 Malathion Substances 0.000 claims description 2
239000005950 Oxamyl Substances 0.000 claims description 2
239000005921 Phosmet Substances 0.000 claims description 2
239000005923 Pirimicarb Substances 0.000 claims description 2
239000005942 Triflumuron Substances 0.000 claims description 2
INISTDXBRIBGOC-CGAIIQECSA-N [cyano-(3-phenoxyphenyl)methyl] (2s)-2-[2-chloro-4-(trifluoromethyl)anilino]-3-methylbutanoate Chemical compound N([C@@H](C(C)C)C(=O)OC(C#N)C=1C=C(OC=2C=CC=CC=2)C=CC=1)C1=CC=C(C(F)(F)F)C=C1Cl INISTDXBRIBGOC-CGAIIQECSA-N 0.000 claims description 2
229960002587 amitraz Drugs 0.000 claims description 2
QXAITBQSYVNQDR-ZIOPAAQOSA-N amitraz Chemical compound C=1C=C(C)C=C(C)C=1/N=C/N(C)\C=N\C1=CC=C(C)C=C1C QXAITBQSYVNQDR-ZIOPAAQOSA-N 0.000 claims description 2
CJJOSEISRRTUQB-UHFFFAOYSA-N azinphos-methyl Chemical group C1=CC=C2C(=O)N(CSP(=S)(OC)OC)N=NC2=C1 CJJOSEISRRTUQB-UHFFFAOYSA-N 0.000 claims description 2
OMFRMAHOUUJSGP-IRHGGOMRSA-N bifenthrin Chemical compound C1=CC=C(C=2C=CC=CC=2)C(C)=C1COC(=O)[C@@H]1[C@H](\C=C(/Cl)C(F)(F)F)C1(C)C OMFRMAHOUUJSGP-IRHGGOMRSA-N 0.000 claims description 2
229960005286 carbaryl Drugs 0.000 claims description 2
DUEPRVBVGDRKAG-UHFFFAOYSA-N carbofuran Chemical compound CNC(=O)OC1=CC=CC2=C1OC(C)(C)C2 DUEPRVBVGDRKAG-UHFFFAOYSA-N 0.000 claims description 2
SBPBAQFWLVIOKP-UHFFFAOYSA-N chlorpyrifos Chemical compound CCOP(=S)(OCC)OC1=NC(Cl)=C(Cl)C=C1Cl SBPBAQFWLVIOKP-UHFFFAOYSA-N 0.000 claims description 2
229960001591 cyfluthrin Drugs 0.000 claims description 2
QQODLKZGRKWIFG-QSFXBCCZSA-N cyfluthrin Chemical compound CC1(C)[C@@H](C=C(Cl)Cl)[C@H]1C(=O)O[C@@H](C#N)C1=CC=C(F)C(OC=2C=CC=CC=2)=C1 QQODLKZGRKWIFG-QSFXBCCZSA-N 0.000 claims description 2
229960005424 cypermethrin Drugs 0.000 claims description 2
KAATUXNTWXVJKI-UHFFFAOYSA-N cypermethrin Chemical compound CC1(C)C(C=C(Cl)Cl)C1C(=O)OC(C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 KAATUXNTWXVJKI-UHFFFAOYSA-N 0.000 claims description 2
229960002483 decamethrin Drugs 0.000 claims description 2
OWZREIFADZCYQD-NSHGMRRFSA-N deltamethrin Chemical compound CC1(C)[C@@H](C=C(Br)Br)[C@H]1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 OWZREIFADZCYQD-NSHGMRRFSA-N 0.000 claims description 2
FHIVAFMUCKRCQO-UHFFFAOYSA-N diazinon Chemical compound CCOP(=S)(OCC)OC1=CC(C)=NC(C(C)C)=N1 FHIVAFMUCKRCQO-UHFFFAOYSA-N 0.000 claims description 2
JXSJBGJIGXNWCI-UHFFFAOYSA-N diethyl 2-[(dimethoxyphosphorothioyl)thio]succinate Chemical compound CCOC(=O)CC(SP(=S)(OC)OC)C(=O)OCC JXSJBGJIGXNWCI-UHFFFAOYSA-N 0.000 claims description 2
MCWXGJITAZMZEV-UHFFFAOYSA-N dimethoate Chemical compound CNC(=O)CSP(=S)(OC)OC MCWXGJITAZMZEV-UHFFFAOYSA-N 0.000 claims description 2
XQUXKZZNEFRCAW-UHFFFAOYSA-N fenpropathrin Chemical compound CC1(C)C(C)(C)C1C(=O)OC(C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 XQUXKZZNEFRCAW-UHFFFAOYSA-N 0.000 claims description 2
KVGLBTYUCJYMND-UHFFFAOYSA-N fonofos Chemical compound CCOP(=S)(CC)SC1=CC=CC=C1 KVGLBTYUCJYMND-UHFFFAOYSA-N 0.000 claims description 2
229960000453 malathion Drugs 0.000 claims description 2
229930002897 methoprene Natural products 0.000 claims description 2
KZAUOCCYDRDERY-UHFFFAOYSA-N oxamyl Chemical compound CNC(=O)ON=C(SC)C(=O)N(C)C KZAUOCCYDRDERY-UHFFFAOYSA-N 0.000 claims description 2
RLBIQVVOMOPOHC-UHFFFAOYSA-N parathion-methyl Chemical group COP(=S)(OC)OC1=CC=C([N+]([O-])=O)C=C1 RLBIQVVOMOPOHC-UHFFFAOYSA-N 0.000 claims description 2
229960000490 permethrin Drugs 0.000 claims description 2
RLLPVAHGXHCWKJ-UHFFFAOYSA-N permethrin Chemical compound CC1(C)C(C=C(Cl)Cl)C1C(=O)OCC1=CC=CC(OC=2C=CC=CC=2)=C1 RLLPVAHGXHCWKJ-UHFFFAOYSA-N 0.000 claims description 2
239000000575 pesticide Substances 0.000 claims description 2
LMNZTLDVJIUSHT-UHFFFAOYSA-N phosmet Chemical compound C1=CC=C2C(=O)N(CSP(=S)(OC)OC)C(=O)C2=C1 LMNZTLDVJIUSHT-UHFFFAOYSA-N 0.000 claims description 2
RGCLLPNLLBQHPF-HJWRWDBZSA-N phosphamidon Chemical compound CCN(CC)C(=O)C(\Cl)=C(/C)OP(=O)(OC)OC RGCLLPNLLBQHPF-HJWRWDBZSA-N 0.000 claims description 2
YFGYUFNIOHWBOB-UHFFFAOYSA-N pirimicarb Chemical compound CN(C)C(=O)OC1=NC(N(C)C)=NC(C)=C1C YFGYUFNIOHWBOB-UHFFFAOYSA-N 0.000 claims description 2
QYMMJNLHFKGANY-UHFFFAOYSA-N profenofos Chemical compound CCCSP(=O)(OCC)OC1=CC=C(Br)C=C1Cl QYMMJNLHFKGANY-UHFFFAOYSA-N 0.000 claims description 2
ZYHMJXZULPZUED-UHFFFAOYSA-N propargite Chemical compound C1=CC(C(C)(C)C)=CC=C1OC1C(OS(=O)OCC#C)CCCC1 ZYHMJXZULPZUED-UHFFFAOYSA-N 0.000 claims description 2
FBQQHUGEACOBDN-UHFFFAOYSA-N quinomethionate Chemical compound N1=C2SC(=O)SC2=NC2=CC(C)=CC=C21 FBQQHUGEACOBDN-UHFFFAOYSA-N 0.000 claims description 2
JUVIOZPCNVVQFO-UHFFFAOYSA-N rotenone Natural products O1C2=C3CC(C(C)=C)OC3=CC=C2C(=O)C2C1COC1=C2C=C(OC)C(OC)=C1 JUVIOZPCNVVQFO-UHFFFAOYSA-N 0.000 claims description 2
JXHJNEJVUNHLKO-UHFFFAOYSA-N sulprofos Chemical compound CCCSP(=S)(OCC)OC1=CC=C(SC)C=C1 JXHJNEJVUNHLKO-UHFFFAOYSA-N 0.000 claims description 2
NFACJZMKEDPNKN-UHFFFAOYSA-N trichlorfon Chemical compound COP(=O)(OC)C(O)C(Cl)(Cl)Cl NFACJZMKEDPNKN-UHFFFAOYSA-N 0.000 claims description 2
NFGXHKASABOEEW-UHFFFAOYSA-N 1-methylethyl 11-methoxy-3,7,11-trimethyl-2,4-dodecadienoate Chemical compound COC(C)(C)CCCC(C)CC=CC(C)=CC(=O)OC(C)C NFGXHKASABOEEW-UHFFFAOYSA-N 0.000 claims 1
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239000005956 Metaldehyde Substances 0.000 claims 1
239000005916 Methomyl Substances 0.000 claims 1
YASYVMFAVPKPKE-UHFFFAOYSA-N acephate Chemical compound COP(=O)(SC)NC(C)=O YASYVMFAVPKPKE-UHFFFAOYSA-N 0.000 claims 1
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QQQYTWIFVNKMRW-UHFFFAOYSA-N diflubenzuron Chemical compound FC1=CC=CC(F)=C1C(=O)NC(=O)NC1=CC=C(Cl)C=C1 QQQYTWIFVNKMRW-UHFFFAOYSA-N 0.000 claims 1
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GBIHOLCMZGAKNG-CGAIIQECSA-N flucythrinate Chemical compound O=C([C@@H](C(C)C)C=1C=CC(OC(F)F)=CC=1)OC(C#N)C(C=1)=CC=CC=1OC1=CC=CC=C1 GBIHOLCMZGAKNG-CGAIIQECSA-N 0.000 claims 1
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HOQADATXFBOEGG-UHFFFAOYSA-N isofenphos Chemical compound CCOP(=S)(NC(C)C)OC1=CC=CC=C1C(=O)OC(C)C HOQADATXFBOEGG-UHFFFAOYSA-N 0.000 claims 1
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UHXUZOCRWCRNSJ-QPJJXVBHSA-N methomyl Chemical compound CNC(=O)O\N=C(/C)SC UHXUZOCRWCRNSJ-QPJJXVBHSA-N 0.000 claims 1
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YWSCPYYRJXKUDB-KAKFPZCNSA-N tralomethrin Chemical compound CC1(C)[C@@H](C(Br)C(Br)(Br)Br)[C@H]1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 YWSCPYYRJXKUDB-KAKFPZCNSA-N 0.000 claims 1
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229910052500 inorganic mineral Inorganic materials 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
235000019357 lignosulphonate Nutrition 0.000 description 1
150000002678 macrocyclic compounds Chemical class 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
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150000004180 methoprene derivatives Chemical class 0.000 description 1
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150000002790 naphthalenes Chemical class 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
RBXVOQPAMPBADW-UHFFFAOYSA-N nitrous acid;phenol Chemical class ON=O.OC1=CC=CC=C1 RBXVOQPAMPBADW-UHFFFAOYSA-N 0.000 description 1
QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
150000002903 organophosphorus compounds Chemical class 0.000 description 1
125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 description 1
239000000546 pharmaceutical excipient Substances 0.000 description 1
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239000008262 pumice Substances 0.000 description 1
150000003242 quaternary ammonium salts Chemical class 0.000 description 1
FFRYUAVNPBUEIC-UHFFFAOYSA-N quinoxalin-2-ol Chemical compound C1=CC=CC2=NC(O)=CN=C21 FFRYUAVNPBUEIC-UHFFFAOYSA-N 0.000 description 1
230000002441 reversible effect Effects 0.000 description 1
JUVIOZPCNVVQFO-HBGVWJBISA-N rotenone Chemical compound O([C@H](CC1=C2O3)C(C)=C)C1=CC=C2C(=O)[C@@H]1[C@H]3COC2=C1C=C(OC)C(OC)=C2 JUVIOZPCNVVQFO-HBGVWJBISA-N 0.000 description 1
239000004576 sand Substances 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
150000004671 saturated fatty acids Chemical class 0.000 description 1
235000003441 saturated fatty acids Nutrition 0.000 description 1
229910052624 sepiolite Inorganic materials 0.000 description 1
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229920002545 silicone oil Polymers 0.000 description 1
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229960000391 sorbitan trioleate Drugs 0.000 description 1
239000003549 soybean oil Substances 0.000 description 1
235000012424 soybean oil Nutrition 0.000 description 1
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238000005507 spraying Methods 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
239000008117 stearic acid Substances 0.000 description 1
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150000004670 unsaturated fatty acids Chemical class 0.000 description 1
235000021122 unsaturated fatty acids Nutrition 0.000 description 1
150000003672 ureas Chemical class 0.000 description 1
235000015112 vegetable and seed oil Nutrition 0.000 description 1
239000008158 vegetable oil Substances 0.000 description 1
235000013311 vegetables Nutrition 0.000 description 1
239000003981 vehicle Substances 0.000 description 1
238000009736 wetting Methods 0.000 description 1
235000014101 wine Nutrition 0.000 description 1
238000010626 work up procedure Methods 0.000 description 1
150000003738 xylenes Chemical class 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- 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
- A01N43/90—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system

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)

DD90343330A 1989-08-10 1990-08-08 Pflanzenakarizide DD298874A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CH294189		1989-08-10

Publications (1)

Publication Number	Publication Date
DD298874A5 true DD298874A5 (de)	1992-03-19

Family

ID=4245075

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD90343330A DD298874A5 (de)	1989-08-10	1990-08-08	Pflanzenakarizide

Country Status (13)

Country	Link
US (1)	US5093358A (fr)
EP (1)	EP0412937A1 (fr)
JP (1)	JPH0383903A (fr)
KR (1)	KR910004095A (fr)
AU (1)	AU6085490A (fr)
BR (1)	BR9003926A (fr)
DD (1)	DD298874A5 (fr)
HU (1)	HUT54467A (fr)
IE (1)	IE902888A1 (fr)
NZ (1)	NZ234817A (fr)
PT (1)	PT94948A (fr)
TR (1)	TR24431A (fr)
ZA (1)	ZA906288B (fr)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPH05112411A (ja) *	1991-08-27	1993-05-07	Nippon Soda Co Ltd	農園芸用殺虫組成物
TR27235A (tr) *	1992-12-15	1994-12-20	Uniroyal Chemical Comp Inc	Sinerjistik ensektisit bilesimleri.
US5352672A (en) *	1993-10-20	1994-10-04	Fmc Corporation	Acaricidal combinations of neem seed extract and bifenthrin
DE10062422A1 (de) *	2000-12-14	2002-06-20	Bayer Ag	Verwendung von Acetyl-CoA Carboxylase zum Identifizieren von insektizid wirksamen Verwendung
KR100834965B1 (ko) *	2001-10-10	2008-06-03	에스케이케미칼주식회사	천연 살충 조성물

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
EP0282455A3 (fr) *	1987-03-12	1990-10-31	Gesellschaft für Biotechnologische Forschung mbH (GBF)	Méthode de préparation d'un dérivé macrocyclique

1990
- 1990-08-01 EP EP90810585A patent/EP0412937A1/fr not_active Ceased
- 1990-08-06 TR TR90/0753A patent/TR24431A/xx unknown
- 1990-08-07 KR KR1019900012235A patent/KR910004095A/ko not_active Withdrawn
- 1990-08-07 US US07/563,776 patent/US5093358A/en not_active Expired - Fee Related
- 1990-08-08 NZ NZ234817A patent/NZ234817A/xx unknown
- 1990-08-08 DD DD90343330A patent/DD298874A5/de not_active IP Right Cessation
- 1990-08-08 PT PT94948A patent/PT94948A/pt not_active Application Discontinuation
- 1990-08-09 ZA ZA906288A patent/ZA906288B/xx unknown
- 1990-08-09 JP JP2211448A patent/JPH0383903A/ja active Pending
- 1990-08-09 IE IE288890A patent/IE902888A1/en unknown
- 1990-08-09 AU AU60854/90A patent/AU6085490A/en not_active Abandoned
- 1990-08-09 HU HU904953A patent/HUT54467A/hu unknown
- 1990-08-09 BR BR909003926A patent/BR9003926A/pt unknown

Also Published As

Publication number	Publication date
ZA906288B (en)	1991-04-24
AU6085490A (en)	1991-02-14
PT94948A (pt)	1991-05-22
TR24431A (tr)	1991-11-01
HUT54467A (en)	1991-03-28
HU904953D0 (en)	1991-01-28
BR9003926A (pt)	1991-09-03
IE902888A1 (en)	1991-02-27
NZ234817A (en)	1991-11-26
JPH0383903A (ja)	1991-04-09
KR910004095A (ko)	1991-03-28
US5093358A (en)	1992-03-03
EP0412937A1 (fr)	1991-02-13

Legal Events

Date	Code	Title	Description
2000-01-20	ENJ	Ceased due to non-payment of renewal fee

Publication	Publication Date	Title
EP0077759B1 (fr)	1987-12-09	Phénylurées
EP0129513B1 (fr)	1988-05-18	Dérivés de l'acide oxamique
EP0097126B1 (fr)	1988-07-27	2-(3-Pyridyl)-1,3,4-oxadiazoles, leur procédé de préparation et leur application comme biocides
DD298874A5 (de)	1992-03-19	Pflanzenakarizide
EP0055213B1 (fr)	1986-02-26	Phénylurées
EP0098800B1 (fr)	1985-08-14	Carbamates
DE3544436A1 (de)	1986-06-19	Neue dioxide
EP0395581A1 (fr)	1990-10-31	N-sulfényl et N-sulfinyl-N,N'-diacylhydrazides
EP0145662B1 (fr)	1987-04-29	Isothiourées
EP0391849B1 (fr)	1995-04-19	Pyridyl-méthylène amino-1,2,4-triazinones
EP0528765B1 (fr)	1997-07-02	Herbicides à base de benzothiazolone
EP0398842A1 (fr)	1990-11-22	Dérivés d'hydrazides
DE3320534A1 (de)	1983-12-15	Carbaminsaeureester
EP0065487B1 (fr)	1985-08-28	Dérivé de phénylurée
EP0274988A2 (fr)	1988-07-20	Dihydrothiadiazoles
EP0053096A1 (fr)	1982-06-02	Bis-carbamates asymétriques, procédé pour leur préparation et leur utilisation dans la lutte contre les organismes nuisibles
EP0164308A1 (fr)	1985-12-11	N-formyl amides d'acide dithiophosphonique
EP0225854A1 (fr)	1987-06-16	Oxadiazinones substituées comme pesticides
DE3235419A1 (de)	1983-04-14	Phenylharnstoffe
DE3641184A1 (de)	1987-06-11	Schaedlingsbekaempfungsmittel
EP0051565A1 (fr)	1982-05-12	N,N-Diméthylcarbamoyl-1-cyclopropyl-3(5)-triazoles-1,2,4-leur préparation et leur utilisation comme pesticides
EP0177455A2 (fr)	1986-04-09	N-benzoylphénylurées
EP0062003A1 (fr)	1982-10-06	Oximecarbamates carboxylés, leur procédé de préparation et leur utilisation comme pesticides
EP0041920A2 (fr)	1981-12-16	Phosphates organiques
DE3033358A1 (de)	1981-03-19	Isovaleriansaere-derivate, verfahren zu deren herstellung und diese enthaltende insektizide und akarizide mittel