OA13185A - Active agents combination exhibiting insecticidal and acaricide properties. - Google Patents

Active agents combination exhibiting insecticidal and acaricide properties. Download PDF

Info

Publication number: OA13185A
Authority: OA; OAPI
Prior art keywords: alkyl; optionally; chlorine; substituted; fluorine
Prior art date: 2003-07-08

Application number

OA1200500376A

Other languages

English (en)

Inventor

Reiner Fischer

Rudiger Fischer

Christian Funke

Wolfgang Thielert

Original Assignee

Bayer Crop Science 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.)

2003-07-08

Filing date

2004-06-25

Publication date

2006-12-13

Family has litigation

First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=33546903&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=OA13185(A) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.

2004-06-25 Application filed by Bayer Crop Science Ag filed Critical Bayer Crop Science Ag

2006-12-13 Publication of OA13185A publication Critical patent/OA13185A/en

Links

230000000749 insecticidal effect Effects 0.000 title claims abstract description 14
230000000895 acaricidal effect Effects 0.000 title claims abstract description 12
239000000642 acaricide Substances 0.000 title abstract description 4
239000013543 active substance Substances 0.000 title abstract 3
230000001747 exhibiting effect Effects 0.000 title description 2
150000001875 compounds Chemical class 0.000 claims description 121
229910052739 hydrogen Inorganic materials 0.000 claims description 84
239000001257 hydrogen Substances 0.000 claims description 84
-1 nitro-substituted phenyl Chemical group 0.000 claims description 76
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical group [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 73
150000002431 hydrogen Chemical class 0.000 claims description 73
239000000460 chlorine Chemical group 0.000 claims description 67
229910052801 chlorine Inorganic materials 0.000 claims description 67
239000000203 mixture Substances 0.000 claims description 55
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 54
229910052731 fluorine Inorganic materials 0.000 claims description 50
239000011737 fluorine Substances 0.000 claims description 50
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 46
229910052794 bromium Inorganic materials 0.000 claims description 46
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 42
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 42
125000004093 cyano group Chemical group *C#N 0.000 claims description 40
YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical group [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 claims description 37
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 32
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 32
239000001301 oxygen Substances 0.000 claims description 32
229910052760 oxygen Inorganic materials 0.000 claims description 32
125000001153 fluoro group Chemical group F* 0.000 claims description 28
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 26
239000005864 Sulphur Substances 0.000 claims description 24
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 22
241000607479 Yersinia pestis Species 0.000 claims description 20
229910052736 halogen Inorganic materials 0.000 claims description 20
150000002367 halogens Chemical group 0.000 claims description 20
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 20
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 16
125000003342 alkenyl group Chemical group 0.000 claims description 15
125000001072 heteroaryl group Chemical group 0.000 claims description 15
125000005842 heteroatom Chemical group 0.000 claims description 15
125000000217 alkyl group Chemical group 0.000 claims description 14
125000003545 alkoxy group Chemical group 0.000 claims description 13
241001465754 Metazoa Species 0.000 claims description 12
125000004183 alkoxy alkyl group Chemical group 0.000 claims description 12
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 12
125000001188 haloalkyl group Chemical group 0.000 claims description 12
125000004076 pyridyl group Chemical group 0.000 claims description 12
229920006395 saturated elastomer Polymers 0.000 claims description 11
229910052799 carbon Inorganic materials 0.000 claims description 10
125000004432 carbon atom Chemical group C* 0.000 claims description 10
125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims description 10
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 10
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 10
125000001544 thienyl group Chemical group 0.000 claims description 10
125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 claims description 10
125000000753 cycloalkyl group Chemical group 0.000 claims description 9
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims description 8
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 8
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 8
125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 8
125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 8
125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 8
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 8
125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 8
125000000547 substituted alkyl group Chemical group 0.000 claims description 8
125000006656 (C2-C4) alkenyl group Chemical group 0.000 claims description 7
238000000034 method Methods 0.000 claims description 7
150000003254 radicals Chemical class 0.000 claims description 7
125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 6
125000004448 alkyl carbonyl group Chemical group 0.000 claims description 6
125000000304 alkynyl group Chemical group 0.000 claims description 6
125000004369 butenyl group Chemical group C(=CCC)* 0.000 claims description 6
125000001309 chloro group Chemical group Cl* 0.000 claims description 6
125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 6
125000004786 difluoromethoxy group Chemical group [H]C(F)(F)O* 0.000 claims description 6
125000004438 haloalkoxy group Chemical group 0.000 claims description 6
PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 claims description 6
125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 6
125000000714 pyrimidinyl group Chemical group 0.000 claims description 6
125000006413 ring segment Chemical group 0.000 claims description 6
125000000335 thiazolyl group Chemical group 0.000 claims description 6
NAYYNDKKHOIIOD-UHFFFAOYSA-N phthalamide Chemical compound NC(=O)C1=CC=CC=C1C(N)=O NAYYNDKKHOIIOD-UHFFFAOYSA-N 0.000 claims description 5
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 4
125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims description 4
125000004106 butoxy group Chemical group [*]OC([H])([H])C([H])([H])C(C([H])([H])[H])([H])[H] 0.000 claims description 4
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 4
125000005448 ethoxyethyl group Chemical group [H]C([H])([H])C([H])([H])OC([H])([H])C([H])([H])* 0.000 claims description 4
125000005745 ethoxymethyl group Chemical group [H]C([H])([H])C([H])([H])OC([H])([H])* 0.000 claims description 4
125000005843 halogen group Chemical group 0.000 claims description 4
229910021645 metal ion Inorganic materials 0.000 claims description 4
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125000003884 phenylalkyl group Chemical group 0.000 claims description 4
125000003356 phenylsulfanyl group Chemical group [*]SC1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims description 4
125000005346 substituted cycloalkyl group Chemical group 0.000 claims description 4
125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 3
239000004606 Fillers/Extenders Substances 0.000 claims description 3
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 3
125000001424 substituent group Chemical group 0.000 claims description 3
125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims description 2
125000004450 alkenylene group Chemical group 0.000 claims description 2
125000005108 alkenylthio group Chemical group 0.000 claims description 2
125000003282 alkyl amino group Chemical group 0.000 claims description 2
125000006350 alkyl thio alkyl group Chemical group 0.000 claims description 2
125000004414 alkyl thio group Chemical group 0.000 claims description 2
125000002947 alkylene group Chemical group 0.000 claims description 2
125000004419 alkynylene group Chemical group 0.000 claims description 2
125000004429 atom Chemical group 0.000 claims description 2
CPPKAGUPTKIMNP-UHFFFAOYSA-N cyanogen fluoride Chemical compound FC#N CPPKAGUPTKIMNP-UHFFFAOYSA-N 0.000 claims description 2
125000001316 cycloalkyl alkyl group Chemical group 0.000 claims description 2
125000005366 cycloalkylthio group Chemical group 0.000 claims description 2
125000004663 dialkyl amino group Chemical group 0.000 claims description 2
125000006351 ethylthiomethyl group Chemical group [H]C([H])([H])C([H])([H])SC([H])([H])* 0.000 claims description 2
125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 claims description 2
125000004433 nitrogen atom Chemical group N* 0.000 claims description 2
125000004430 oxygen atom Chemical group O* 0.000 claims description 2
125000005359 phenoxyalkyl group Chemical group 0.000 claims description 2
125000002071 phenylalkoxy group Chemical group 0.000 claims description 2
239000004094 surface-active agent Substances 0.000 claims description 2
229910052721 tungsten Inorganic materials 0.000 claims description 2
229910052727 yttrium Inorganic materials 0.000 claims description 2
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238000004519 manufacturing process Methods 0.000 claims 1
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238000009472 formulation Methods 0.000 description 12
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HOWHQWFXSLOJEF-MGZLOUMQSA-N systemin Chemical compound NCCCC[C@H](N)C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CC(O)=O)C(=O)OC(=O)[C@@H]1CCCN1C(=O)[C@H]1N(C(=O)[C@H](CC(O)=O)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CO)NC(=O)[C@H]2N(CCC2)C(=O)[C@H]2N(CCC2)C(=O)[C@H](CCCCN)NC(=O)[C@H](CO)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@@H](NC(=O)[C@H](C)N)C(C)C)CCC1 HOWHQWFXSLOJEF-MGZLOUMQSA-N 0.000 description 1
108010050014 systemin Proteins 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
IROINLKCQGIITA-UHFFFAOYSA-N terbutryn Chemical compound CCNC1=NC(NC(C)(C)C)=NC(SC)=N1 IROINLKCQGIITA-UHFFFAOYSA-N 0.000 description 1
BAKXBZPQTXCKRR-UHFFFAOYSA-N thiodicarb Chemical compound CSC(C)=NOC(=O)NSNC(=O)ON=C(C)SC BAKXBZPQTXCKRR-UHFFFAOYSA-N 0.000 description 1
QERYCTSHXKAMIS-UHFFFAOYSA-N thiophene-2-carboxylic acid Chemical compound OC(=O)C1=CC=CS1 QERYCTSHXKAMIS-UHFFFAOYSA-N 0.000 description 1
KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical class CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 description 1
229960002447 thiram Drugs 0.000 description 1
OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
HYVWIQDYBVKITD-UHFFFAOYSA-N tolylfluanid Chemical compound CN(C)S(=O)(=O)N(SC(F)(Cl)Cl)C1=CC=C(C)C=C1 HYVWIQDYBVKITD-UHFFFAOYSA-N 0.000 description 1
STCOOQWBFONSKY-UHFFFAOYSA-N tributyl phosphate Chemical compound CCCCOP(=O)(OCCCC)OCCCC STCOOQWBFONSKY-UHFFFAOYSA-N 0.000 description 1
WVZPYZMQQDNINJ-UHFFFAOYSA-N tributyl(butylstannyloxy)stannane Chemical class CCCC[SnH](CCCC)O[SnH](CCCC)CCCC WVZPYZMQQDNINJ-UHFFFAOYSA-N 0.000 description 1
HFFZSMFXOBHQLV-UHFFFAOYSA-M tributylstannyl dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)CCCC HFFZSMFXOBHQLV-UHFFFAOYSA-M 0.000 description 1
229940036248 turpentine Drugs 0.000 description 1
229930195735 unsaturated hydrocarbon Natural products 0.000 description 1
235000013311 vegetables Nutrition 0.000 description 1
238000005406 washing Methods 0.000 description 1
239000002699 waste material Substances 0.000 description 1
210000002268 wool Anatomy 0.000 description 1
239000008096 xylene Substances 0.000 description 1
229910052725 zinc Inorganic materials 0.000 description 1
239000011701 zinc Substances 0.000 description 1
239000011787 zinc oxide Substances 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
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
- A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
- A01N43/04—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
- A01N43/06—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings
- A01N43/08—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings with oxygen as the ring hetero atom
- 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
- A01N41/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a sulfur atom bound to a hetero atom
- A01N41/02—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a sulfur atom bound to a hetero atom containing a sulfur-to-oxygen double bond
- A01N41/10—Sulfones; Sulfoxides
- 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
- A01N47/08—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 the carbon atom having one or more single bonds to nitrogen atoms
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents

Landscapes

Life Sciences & Earth Sciences (AREA)
Health & Medical Sciences (AREA)
General Health & Medical Sciences (AREA)
Dentistry (AREA)
Wood Science & Technology (AREA)
Environmental Sciences (AREA)
Zoology (AREA)
Engineering & Computer Science (AREA)
Plant Pathology (AREA)
Pest Control & Pesticides (AREA)
Agronomy & Crop Science (AREA)
Veterinary Medicine (AREA)
Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
Public Health (AREA)
Chemical & Material Sciences (AREA)
Pharmacology & Pharmacy (AREA)
Organic Chemistry (AREA)
Animal Behavior & Ethology (AREA)
Tropical Medicine & Parasitology (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
General Chemical & Material Sciences (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)

OA1200500376A 2003-07-08 2004-06-25 Active agents combination exhibiting insecticidal and acaricide properties. OA13185A (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE10330724A DE10330724A1 (de)	2003-07-08	2003-07-08	Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften

Publications (1)

Publication Number	Publication Date
OA13185A true OA13185A (en)	2006-12-13

Family

ID=33546903

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
OA1200500376A OA13185A (en)	2003-07-08	2004-06-25	Active agents combination exhibiting insecticidal and acaricide properties.

Country Status (18)

Country	Link
US (1)	US8143193B2 (pt)
EP (1)	EP1646281B1 (pt)
JP (1)	JP4733027B2 (pt)
KR (1)	KR101122099B1 (pt)
CN (1)	CN100490646C (pt)
AR (1)	AR045036A1 (pt)
AT (1)	ATE362700T1 (pt)
AU (1)	AU2004255412B2 (pt)
BR (1)	BRPI0411862B1 (pt)
DE (2)	DE10330724A1 (pt)
ES (1)	ES2286641T3 (pt)
IL (1)	IL172841A0 (pt)
MX (1)	MXPA06000200A (pt)
OA (1)	OA13185A (pt)
PT (1)	PT1646281E (pt)
TW (1)	TWI341715B (pt)
WO (1)	WO2005004603A1 (pt)
ZA (1)	ZA200600099B (pt)

Families Citing this family (32)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE10330724A1 (de)	2003-07-08	2005-01-27	Bayer Cropscience Ag	Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften
DE102004011007A1 (de) *	2004-03-06	2005-09-22	Bayer Cropscience Ag	Suspensionskonzentrate auf Ölbasis
DE102004011006A1 (de) *	2004-03-06	2005-09-22	Bayer Cropscience Ag	Suspensionskonzentrate auf Ölbasis
DE102004035134A1 (de) *	2004-07-20	2006-02-16	Bayer Cropscience Ag	Selektive Insektizide auf Basis von Halogenalkylnicotinsäurederivaten, Anthranilsäureamiden oder Phthalsäurediamiden und Safenern
AU2005279429B2 (en) *	2004-08-31	2010-10-28	Bayer Cropscience Ag	Optically active phthalamides
DE102004044827A1 (de)	2004-09-16	2006-03-23	Bayer Cropscience Ag	Jod-phenylsubstituierte cyclische Ketoenole
DE102004053192A1 (de) *	2004-11-04	2006-05-11	Bayer Cropscience Ag	2-Alkoxy-6-alkyl-phenyl substituierte spirocyclische Tetramsäure-Derivate
DE102004053191A1 (de) *	2004-11-04	2006-05-11	Bayer Cropscience Ag	2,6-Diethyl-4-methyl-phenyl substituierte Tetramsäure-Derivate
DE102005008033A1 (de) *	2005-02-22	2006-08-24	Bayer Cropscience Ag	Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften
JP2006347936A (ja) *	2005-06-15	2006-12-28	Bayer Cropscience Ag	殺虫性ベンズアニリド類
DE102005048539A1 (de) *	2005-10-11	2007-04-12	Bayer Cropscience Ag	Suspensionskonzentrate auf Ölbasis
DE102006010208A1 (de) *	2006-03-06	2007-09-13	Bayer Cropscience Ag	Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften
DE102006015197A1 (de) *	2006-03-06	2007-09-13	Bayer Cropscience Ag	Wirkstoffkombination mit insektiziden Eigenschaften
DE102006010206A1 (de) *	2006-03-06	2007-09-13	Bayer Cropscience Ag	Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften
DE102006014482A1 (de) *	2006-03-29	2007-10-04	Bayer Cropscience Ag	Wirkstoffkombinationen mit insektiziden Eigenschaften
DE102006025874A1 (de)	2006-06-02	2007-12-06	Bayer Cropscience Ag	Alkoxyalkyl-substituierte cyclische Ketoenole
DE102006027731A1 (de)	2006-06-16	2007-12-20	Bayer Cropscience Ag	Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften
DE102006031976A1 (de) *	2006-07-11	2008-01-17	Bayer Cropscience Ag	Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften
US20090281157A1 (en) *	2006-07-11	2009-11-12	Bayer Cropscience Ag	Active Ingredient Combinations With Insecticidal and Acaricidal Properties
DE102006031978A1 (de) *	2006-07-11	2008-01-17	Bayer Cropscience Ag	Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften
DE102006033154A1 (de)	2006-07-18	2008-01-24	Bayer Cropscience Ag	Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften
DE102006057037A1 (de) *	2006-12-04	2008-06-05	Bayer Cropscience Ag	cis-Alkoxyspirocyclische biphenylsubstituierte Tetramsäure-Derivate
EP2008519A1 (de) *	2007-06-28	2008-12-31	Bayer CropScience AG	Verwendung von Wirkstoffkombinationen mit insektiziden Eigenschaften zur Bekämpfung von tierischen Schädlingen aus der Familie der Stinkwanzen
EP2011394A1 (de) *	2007-07-03	2009-01-07	Bayer CropScience AG	Verwendung von Tetramsäure - Derivaten zur Bekämpfung von virusübertragenden Vektoren
KR101457993B1 (ko)	2007-12-20	2014-11-04	바이엘 크롭사이언스 아게	선충을 구제하기 위한 테트람산 유도체의 용도
EP2127522A1 (de)	2008-05-29	2009-12-02	Bayer CropScience AG	Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften
US8683346B2 (en) *	2008-11-17	2014-03-25	Sap Portals Israel Ltd.	Client integration of information from a supplemental server into a portal
DE102009028001A1 (de)	2009-07-24	2011-01-27	Bayer Cropscience Ag	Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften
US20110200571A1 (en) *	2010-02-12	2011-08-18	Bell John W	Methods for Reducing Nematode Damage to Plants
JPWO2012169473A1 (ja)	2011-06-06	2015-02-23	日本農薬株式会社	植物生長調節剤及びその使用方法
KR20140031950A (ko)	2011-06-29	2014-03-13	니혼노야쿠가부시키가이샤	농원예용 살충제 조성물 및 그 사용 방법
CN114149433A (zh) *	2020-09-07	2022-03-08	海利尔药业集团股份有限公司	一种含氮螺环衍生物或其作为农药可接受的盐、组合物及其用途

Family Cites Families (61)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3364177A (en)	1966-02-21	1968-01-16	Dow Chemical Co	Curing epoxy resins with aminomethylated diphenyl oxides
FI762480A7 (pt)	1975-09-15	1977-03-16	Du Pont
IL79360A (en)	1985-07-12	1993-02-21	Ciba Geigy Ag	Aleyrodidae-controlling compositions containing n-(4-phenoxy-2,6- diisopropylphenyl) -n)-tert- butylthiourea as active agent
CA1300137C (en)	1985-12-27	1992-05-05	Hiroshi Hamaguchi	Pyrazole oxime derivative and its production and use
US5010098A (en)	1987-07-29	1991-04-23	American Cyanamid Company	Arylpyrrole insecticidal acaricidal and nematicidal agents and methods for the preparation thereof
US4985063A (en)	1988-08-20	1991-01-15	Bayer Aktiengesellschaft	3-aryl-pyrrolidine-2,4-diones
ES2063108T3 (es)	1989-01-07	1995-01-01	Bayer Ag	Derivados de 3-aril-pirrolidin-2,4-diona.
DE3929087A1 (de)	1989-09-01	1991-03-07	Bayer Ag	3-aryl-pyrrolidin-2,4-dion-derivate
DE4032090A1 (de)	1990-02-13	1991-08-14	Bayer Ag	Polycyclische 3-aryl-pyrrolidin-2,4-dion-derivate
DE4004496A1 (de)	1990-02-14	1991-08-22	Bayer Ag	3-aryl-pyrrolidin-2,4-dion-derivate
DE4107394A1 (de)	1990-05-10	1991-11-14	Bayer Ag	1-h-3-aryl-pyrrolidin-2,4-dion-derivate
DE4121365A1 (de)	1991-06-28	1993-01-14	Bayer Ag	Substituierte 1-h-3-aryl-pyrrolidin-2,4-dion-derivate
BR9206803A (pt)	1991-11-22	1995-05-02	Uniroyal Chemical Ltd	Derivados inseticidas de fenilhidrazina
US5478855A (en)	1992-04-28	1995-12-26	Yashima Chemical Industry Co., Ltd.	2-(2,6-difluorophenyl)-4-(2-ethoxy-4-tert-butylphenyl)-2-oxazoline
AU666040B2 (en)	1992-10-28	1996-01-25	Bayer Aktiengesellschaft	Substituted 1-H-3-aryl-pyrrolidine-2,4-dione derivatives
DE4306259A1 (de)	1993-03-01	1994-09-08	Bayer Ag	Dialkyl-1-H-3-(2,4-dimethylphenyl)-pyrrolidin-2,4-dione, ihre Herstellung und ihre Verwendung
DE4306257A1 (de)	1993-03-01	1994-09-08	Bayer Ag	Substituierte 1-H-3-Phenyl-5-cycloalkylpyrrolidin-2,4-dione, ihre Herstellung und ihre Verwendung
US5981567A (en)	1993-07-02	1999-11-09	Bayer Aktiengesellschaft	Substituted spiroheterocyclic 1h-3-aryl-pyrrolidine-2,4-dione derivatives and their use as pesticides
DE59407886D1 (en)	1993-07-05	1999-04-08	Bayer Ag	Substituierte aryl-ketoenolheterocyclen
DE4425617A1 (de)	1994-01-28	1995-08-03	Bayer Ag	1-H-3-Aryl-pyrrolidin-2,4-dion-Derivate
DE4431730A1 (de)	1994-02-09	1995-08-10	Bayer Ag	Substituierte 1H-3-Aryl-pyrrolidin-2,4-dion-Derivate
ES2190786T3 (es)	1994-04-05	2003-08-16	Bayer Cropscience Ag	1-h-3-aril-pirrolidin-2,4-dionas alcoxi-alquil-substituidas como herbicidas y pesticidas.
ES2224156T3 (es)	1995-02-13	2005-03-01	Bayer Cropscience Ag	1,2-cetoenoles heterociclicos 2-fenil- substituidos como herbicidas y pesticidas.
ES2184858T3 (es)	1995-05-09	2003-04-16	Bayer Cropscience Ag	Cetoenoles alquil-dihalogenofenil substituidos como pesticidas y herbicidas.
TR199701708T1 (xx)	1995-06-28	1998-04-21	Bayer Aktingesellschaft	2,4,5-Triikameli fenilketoenoller.
WO1997002243A1 (de)	1995-06-30	1997-01-23	Bayer Aktiengesellschaft	Dialkyl-halogenphenylsubstituierte ketoenole zur verwendung als herbizide und pestizide
AU725852B2 (en)	1996-04-02	2000-10-19	Bayer Aktiengesellschaft	Substituted phenylketoenols as pesticides and herbicides
ES2251022T3 (es)	1996-05-10	2006-04-16	Bayer Cropscience Ag	Nuevos piridilcetoenoles sustituidos.
DK0915846T3 (da) *	1996-08-05	2003-08-11	Bayer Cropscience Ag	2- og 2,5-substituerede phenylketoenoler
DE19632126A1 (de)	1996-08-09	1998-02-12	Bayer Ag	Phenylsubstituierte cyclische Ketoenole
DE19651686A1 (de)	1996-12-12	1998-06-18	Bayer Ag	Neue substituierte Phenylketoenole
DE19742492A1 (de)	1997-09-26	1999-04-01	Bayer Ag	Spirocyclische Phenylketoenole
DE19749720A1 (de)	1997-11-11	1999-05-12	Bayer Ag	Neue substituierte Phenylketoenole
TW515786B (en)	1997-11-25	2003-01-01	Nihon Nohyaku Co Ltd	Phthalic acid diamide derivatives, agricultural and horticultural insecticides, and a method for application of the insecticides
DE19808261A1 (de)	1998-02-27	1999-10-28	Bayer Ag	Arylphenylsubstituierte cyclische Ketoenole
DE19813354A1 (de)	1998-03-26	1999-09-30	Bayer Ag	Arylphenylsubstituierte cyclische Ketoenole
DE19818732A1 (de)	1998-04-27	1999-10-28	Bayer Ag	Arylphenylsubstituierte cyclische Ketoenole
CZ299375B6 (cs)	1998-11-30	2008-07-09	Nihon Nohyaku Co., Ltd.	Ftalamidové deriváty nebo jejich soli, zemedelsko-zahradnický insekticid je obsahující a jeho použití
CZ20014679A3 (cs)	1999-06-24	2002-04-17	Nihon Nohyaku Co., Ltd.	Diamidové deriváty heterocyklické dikarboxylové kyseliny, zemědělské a zahradnické insekticidy a způsob jejich pouľití
ATE248152T1 (de)	1999-06-25	2003-09-15	Nihon Nohyaku Co Ltd	Benzamid-derivate, insektizide zur verwendung im agrar- und gartenbereich und ihre verwendung
AR030154A1 (es)	1999-07-05	2003-08-13	Nihon Nohyaku Co Ltd	Derivado de ftalamida, derivado de amina heterociclico util como intermediario para la produccion del mismo, insecticida agrohorticola y metodo para utilizar dicho insecticida
EP1215200B1 (en)	1999-09-24	2005-03-16	Nihon Nohyaku Co., Ltd.	Aromatic diamide derivatives or salts thereof, agricultural/horticultural chemicals and method of using the same
DE19946625A1 (de)	1999-09-29	2001-04-05	Bayer Ag	Trifluormethylsubstituierte spirocyclische Ketoenole
US6924008B2 (en) *	1999-12-17	2005-08-02	Daicel Chemical Industries, Ltd.	Curable resin composition, a method for the preparation thereof, and a coated article thereof
US7256192B2 (en)	1999-12-22	2007-08-14	Nihon Nohyaku Co., Ltd.	Aromatic diamide derivatives, chemicals for agricultural or horticultural use and usage thereof
DE10016544A1 (de)	2000-04-03	2001-10-11	Bayer Ag	C2-phenylsubstituierte Ketoenole
JP4573075B2 (ja)	2000-05-26	2010-11-04	日本農薬株式会社	フタル酸ジアミド誘導体及び農園芸用殺虫剤並びにその使用方法
DE10049804A1 (de) *	2000-10-09	2002-04-18	Bayer Ag	Wirkstoffkombinationen mit fungiziden und akariziden Eigenschaften
EP1360190B1 (de)	2001-02-06	2005-09-07	Bayer CropScience AG	Phthalsäurediamide, ein verfahren zu ihrer herstellung und ihre verwendung als schädlingsbekämpfungsmittel
JP4348669B2 (ja) *	2001-04-17	2009-10-21	日本農薬株式会社	有害生物防除剤組成物及びその使用方法
TWI304324B (en) *	2001-04-17	2008-12-21	Nihon Nohyaku Co Ltd	Pestcide composition and uses thereof
EP1389612A4 (en)	2001-04-26	2004-06-02	Nihon Nohyaku Co Ltd	PHTHALAMIDE DERIVATIVES, INSECTICIDES FOR USE IN AGRICULTURE AND GARDENING AND METHOD FOR THE USE THEREOF
WO2002088075A1 (fr)	2001-04-26	2002-11-07	Nihon Nohyaku Co., Ltd.	Derives de phtalamide, insecticide a usage agricole et horticole et leur procede d'application
WO2002094766A1 (en)	2001-05-18	2002-11-28	Nihon Nohyaku Co., Ltd.	Phthalamide derivative, agricultural or horticultural insecticide, and use thereof
AR035884A1 (es)	2001-05-18	2004-07-21	Nihon Nohyaku Co Ltd	Derivado de amida aromatico sustituido, derivado de amina aromatico sustituido con un grupo fluoroalquilo util como intermediario para obtener el mismo, insecticida para agrohorticultura que lo contiene y metodo para usar este ultimo
DE10248257A1 (de)	2002-10-16	2004-04-29	Bayer Cropscience Ag	Wirkstoffkombinationen im insektiziden und akariziden Eigenschaften
DE10330724A1 (de)	2003-07-08	2005-01-27	Bayer Cropscience Ag	Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften
DE102004035134A1 (de)	2004-07-20	2006-02-16	Bayer Cropscience Ag	Selektive Insektizide auf Basis von Halogenalkylnicotinsäurederivaten, Anthranilsäureamiden oder Phthalsäurediamiden und Safenern
AU2005279429B2 (en)	2004-08-31	2010-10-28	Bayer Cropscience Ag	Optically active phthalamides
DE102005059466A1 (de)	2005-12-13	2007-06-14	Bayer Cropscience Ag	Insektizide Zusammensetzungen mit verbesserter Wirkung
DE102005059467A1 (de)	2005-12-13	2007-06-14	Bayer Cropscience Ag	Insektizide Zusammensetzungen mit verbesserter Wirkung

2003
- 2003-07-08 DE DE10330724A patent/DE10330724A1/de not_active Withdrawn
2004
- 2004-06-25 CN CNB2004800194459A patent/CN100490646C/zh not_active Expired - Fee Related
- 2004-06-25 US US10/563,794 patent/US8143193B2/en not_active Expired - Fee Related
- 2004-06-25 OA OA1200500376A patent/OA13185A/en unknown
- 2004-06-25 WO PCT/EP2004/006914 patent/WO2005004603A1/de not_active Ceased
- 2004-06-25 AU AU2004255412A patent/AU2004255412B2/en not_active Ceased
- 2004-06-25 KR KR1020067000289A patent/KR101122099B1/ko not_active Expired - Fee Related
- 2004-06-25 DE DE502004003896T patent/DE502004003896D1/de not_active Expired - Fee Related
- 2004-06-25 AT AT04740323T patent/ATE362700T1/de not_active IP Right Cessation
- 2004-06-25 EP EP04740323A patent/EP1646281B1/de not_active Expired - Lifetime
- 2004-06-25 JP JP2006518040A patent/JP4733027B2/ja not_active Expired - Fee Related
- 2004-06-25 MX MXPA06000200A patent/MXPA06000200A/es active IP Right Grant
- 2004-06-25 PT PT04740323T patent/PT1646281E/pt unknown
- 2004-06-25 ES ES04740323T patent/ES2286641T3/es not_active Expired - Lifetime
- 2004-06-25 BR BRPI0411862-6A patent/BRPI0411862B1/pt not_active IP Right Cessation
- 2004-07-07 TW TW093120287A patent/TWI341715B/zh not_active IP Right Cessation
- 2004-07-07 AR ARP040102390A patent/AR045036A1/es active IP Right Grant
2005
- 2005-12-27 IL IL172841A patent/IL172841A0/en active IP Right Grant
2006
- 2006-01-04 ZA ZA200600099A patent/ZA200600099B/xx unknown

Also Published As

Publication number	Publication date
MXPA06000200A (es)	2006-04-11
AU2004255412A1 (en)	2005-01-20
US8143193B2 (en)	2012-03-27
KR101122099B1 (ko)	2012-03-19
PT1646281E (pt)	2007-08-07
CN100490646C (zh)	2009-05-27
ATE362700T1 (de)	2007-06-15
TWI341715B (en)	2011-05-11
EP1646281A1 (de)	2006-04-19
CN1819767A (zh)	2006-08-16
IL172841A0 (en)	2006-06-11
KR20060032999A (ko)	2006-04-18
AR045036A1 (es)	2005-10-12
EP1646281B1 (de)	2007-05-23
TW200526121A (en)	2005-08-16
WO2005004603A1 (de)	2005-01-20
ZA200600099B (en)	2007-03-28
AU2004255412B2 (en)	2010-04-08
BRPI0411862A (pt)	2006-08-08
JP2009513501A (ja)	2009-04-02
US20070265266A1 (en)	2007-11-15
ES2286641T3 (es)	2007-12-01
DE502004003896D1 (de)	2007-07-05
DE10330724A1 (de)	2005-01-27
BRPI0411862B1 (pt)	2014-10-14
JP4733027B2 (ja)	2011-07-27

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