MXPA05000114A - Fenilbenzamidas. - Google Patents
Fenilbenzamidas.Info
- Publication number
- MXPA05000114A MXPA05000114A MXPA05000114A MXPA05000114A MXPA05000114A MX PA05000114 A MXPA05000114 A MX PA05000114A MX PA05000114 A MXPA05000114 A MX PA05000114A MX PA05000114 A MXPA05000114 A MX PA05000114A MX PA05000114 A MXPA05000114 A MX PA05000114A
- Authority
- MX
- Mexico
- Prior art keywords
- formula
- phenyl
- plants
- methyl
- phenylbenzamides
- Prior art date
Links
- ZVSKZLHKADLHSD-UHFFFAOYSA-N benzanilide Chemical class C=1C=CC=CC=1C(=O)NC1=CC=CC=C1 ZVSKZLHKADLHSD-UHFFFAOYSA-N 0.000 title abstract 2
- 244000005700 microbiome Species 0.000 claims abstract description 18
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 14
- 239000001257 hydrogen Substances 0.000 claims abstract description 12
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 12
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims abstract description 10
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims abstract description 10
- -1 1,3-dimethylbutyl Chemical group 0.000 claims description 35
- 238000000034 method Methods 0.000 claims description 30
- GTKIGDZXPDCIKR-UHFFFAOYSA-N 2-phenylbenzamide Chemical class NC(=O)C1=CC=CC=C1C1=CC=CC=C1 GTKIGDZXPDCIKR-UHFFFAOYSA-N 0.000 claims description 20
- 230000008569 process Effects 0.000 claims description 19
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 claims description 14
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 11
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 9
- KXDAEFPNCMNJSK-UHFFFAOYSA-N Benzamide Chemical compound NC(=O)C1=CC=CC=C1 KXDAEFPNCMNJSK-UHFFFAOYSA-N 0.000 claims description 6
- 239000003795 chemical substances by application Substances 0.000 claims description 5
- 239000002841 Lewis acid Substances 0.000 claims description 4
- 150000001336 alkenes Chemical class 0.000 claims description 4
- PASDCCFISLVPSO-UHFFFAOYSA-N benzoyl chloride Chemical compound ClC(=O)C1=CC=CC=C1 PASDCCFISLVPSO-UHFFFAOYSA-N 0.000 claims description 4
- 125000002346 iodo group Chemical group I* 0.000 claims description 4
- 150000007517 lewis acids Chemical class 0.000 claims description 4
- IOIRBHLKTRPQBR-UHFFFAOYSA-N 2-bromo-n-[2-(4-methylpentan-2-yl)phenyl]benzamide Chemical compound CC(C)CC(C)C1=CC=CC=C1NC(=O)C1=CC=CC=C1Br IOIRBHLKTRPQBR-UHFFFAOYSA-N 0.000 claims description 3
- IESUPPBKWJHHEW-UHFFFAOYSA-N 2-chloro-n-[2-(4-methylpentan-2-yl)phenyl]benzamide Chemical compound CC(C)CC(C)C1=CC=CC=C1NC(=O)C1=CC=CC=C1Cl IESUPPBKWJHHEW-UHFFFAOYSA-N 0.000 claims description 3
- GMMOMHSLRVQSRX-UHFFFAOYSA-N 2-iodo-n-[2-(4-methylpentan-2-yl)phenyl]benzamide Chemical compound CC(C)CC(C)C1=CC=CC=C1NC(=O)C1=CC=CC=C1I GMMOMHSLRVQSRX-UHFFFAOYSA-N 0.000 claims description 3
- 239000004606 Fillers/Extenders Substances 0.000 claims description 3
- 150000001448 anilines Chemical class 0.000 claims description 3
- 125000001246 bromo group Chemical group Br* 0.000 claims description 3
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 3
- 239000003085 diluting agent Substances 0.000 claims description 3
- 239000004094 surface-active agent Substances 0.000 claims description 3
- 239000000126 substance Substances 0.000 abstract description 5
- 238000004519 manufacturing process Methods 0.000 abstract description 3
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 abstract description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical group [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 abstract description 2
- 229910052794 bromium Inorganic materials 0.000 abstract description 2
- 239000000460 chlorine Chemical group 0.000 abstract description 2
- 229910052801 chlorine Inorganic materials 0.000 abstract description 2
- 239000011630 iodine Chemical group 0.000 abstract description 2
- 229910052740 iodine Chemical group 0.000 abstract description 2
- 150000001648 bromium Chemical group 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
- 239000013067 intermediate product Substances 0.000 abstract 1
- 241000196324 Embryophyta Species 0.000 description 88
- 150000001875 compounds Chemical class 0.000 description 36
- 238000012360 testing method Methods 0.000 description 29
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 21
- 238000002360 preparation method Methods 0.000 description 20
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 19
- 230000000694 effects Effects 0.000 description 19
- 239000000203 mixture Substances 0.000 description 16
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 15
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 15
- 239000003995 emulsifying agent Substances 0.000 description 15
- 239000002904 solvent Substances 0.000 description 15
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 15
- 230000001012 protector Effects 0.000 description 14
- 240000008042 Zea mays Species 0.000 description 11
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 11
- 238000006243 chemical reaction Methods 0.000 description 11
- ZMXDDKWLCZADIW-UHFFFAOYSA-N Vilsmeier-Haack reagent Natural products CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 10
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 10
- 235000005822 corn Nutrition 0.000 description 10
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 10
- LPZZJKBLKQOBMZ-UHFFFAOYSA-N 2-(4-methylpentan-2-yl)aniline Chemical compound CC(C)CC(C)C1=CC=CC=C1N LPZZJKBLKQOBMZ-UHFFFAOYSA-N 0.000 description 9
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 9
- 241000233866 Fungi Species 0.000 description 9
- 229920000742 Cotton Polymers 0.000 description 8
- 244000299507 Gossypium hirsutum Species 0.000 description 8
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- 244000038559 crop plants Species 0.000 description 7
- 238000009472 formulation Methods 0.000 description 7
- 238000011081 inoculation Methods 0.000 description 7
- 229920000151 polyglycol Polymers 0.000 description 7
- 239000010695 polyglycol Substances 0.000 description 7
- 108090000623 proteins and genes Proteins 0.000 description 7
- 239000000725 suspension Substances 0.000 description 7
- WSSSPWUEQFSQQG-UHFFFAOYSA-N 4-methyl-1-pentene Chemical compound CC(C)CC=C WSSSPWUEQFSQQG-UHFFFAOYSA-N 0.000 description 6
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 6
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 125000002877 alkyl aryl group Chemical group 0.000 description 6
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 6
- 239000012141 concentrate Substances 0.000 description 6
- 239000008187 granular material Substances 0.000 description 6
- 239000004009 herbicide Substances 0.000 description 6
- 239000002689 soil Substances 0.000 description 6
- 241000894006 Bacteria Species 0.000 description 5
- 235000010469 Glycine max Nutrition 0.000 description 5
- 241000221300 Puccinia Species 0.000 description 5
- 239000011248 coating agent Substances 0.000 description 5
- 238000000576 coating method Methods 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 5
- 238000001035 drying Methods 0.000 description 5
- 238000011156 evaluation Methods 0.000 description 5
- 238000001704 evaporation Methods 0.000 description 5
- 230000008020 evaporation Effects 0.000 description 5
- 230000002363 herbicidal effect Effects 0.000 description 5
- 239000012074 organic phase Substances 0.000 description 5
- 229910000027 potassium carbonate Inorganic materials 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- 230000009261 transgenic effect Effects 0.000 description 5
- MXIUWSYTQJLIKE-UHFFFAOYSA-N 2-(trifluoromethyl)benzoyl chloride Chemical compound FC(F)(F)C1=CC=CC=C1C(Cl)=O MXIUWSYTQJLIKE-UHFFFAOYSA-N 0.000 description 4
- 244000068988 Glycine max Species 0.000 description 4
- 240000005979 Hordeum vulgare Species 0.000 description 4
- 235000007340 Hordeum vulgare Nutrition 0.000 description 4
- 235000011430 Malus pumila Nutrition 0.000 description 4
- 235000015103 Malus silvestris Nutrition 0.000 description 4
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 4
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 4
- 240000003768 Solanum lycopersicum Species 0.000 description 4
- 244000061456 Solanum tuberosum Species 0.000 description 4
- 235000002595 Solanum tuberosum Nutrition 0.000 description 4
- 241000209140 Triticum Species 0.000 description 4
- 235000021307 Triticum Nutrition 0.000 description 4
- 235000013399 edible fruits Nutrition 0.000 description 4
- 150000002148 esters Chemical class 0.000 description 4
- 239000000417 fungicide Substances 0.000 description 4
- 238000010353 genetic engineering Methods 0.000 description 4
- 239000003292 glue Substances 0.000 description 4
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- 239000007788 liquid Substances 0.000 description 4
- 235000010755 mineral Nutrition 0.000 description 4
- 238000012986 modification Methods 0.000 description 4
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- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 239000007858 starting material Substances 0.000 description 4
- 239000002023 wood Substances 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- NZCKTGCKFJDGFD-UHFFFAOYSA-N 2-bromobenzoyl chloride Chemical group ClC(=O)C1=CC=CC=C1Br NZCKTGCKFJDGFD-UHFFFAOYSA-N 0.000 description 3
- ONIKNECPXCLUHT-UHFFFAOYSA-N 2-chlorobenzoyl chloride Chemical compound ClC(=O)C1=CC=CC=C1Cl ONIKNECPXCLUHT-UHFFFAOYSA-N 0.000 description 3
- MVIVDSWUOGNODP-UHFFFAOYSA-N 2-iodobenzoyl chloride Chemical compound ClC(=O)C1=CC=CC=C1I MVIVDSWUOGNODP-UHFFFAOYSA-N 0.000 description 3
- 241000223600 Alternaria Species 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
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- 240000002791 Brassica napus Species 0.000 description 3
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- QMMFVYPAHWMCMS-UHFFFAOYSA-N Dimethyl sulfide Chemical compound CSC QMMFVYPAHWMCMS-UHFFFAOYSA-N 0.000 description 3
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- 235000007688 Lycopersicon esculentum Nutrition 0.000 description 3
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- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- 241000228453 Pyrenophora Species 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
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- NYPJDWWKZLNGGM-UHFFFAOYSA-N fenvalerate Aalpha Natural products 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 description 3
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- KAATUXNTWXVJKI-NSHGMRRFSA-N (1R)-cis-(alphaS)-cypermethrin Chemical compound CC1(C)[C@@H](C=C(Cl)Cl)[C@H]1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 KAATUXNTWXVJKI-NSHGMRRFSA-N 0.000 description 2
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- WNZQDUSMALZDQF-UHFFFAOYSA-N 2-benzofuran-1(3H)-one Chemical compound C1=CC=C2C(=O)OCC2=C1 WNZQDUSMALZDQF-UHFFFAOYSA-N 0.000 description 2
- AKPLYNMWGYVIRE-UHFFFAOYSA-N 2-chloro-N-[2-(4,4-dimethylhexan-2-yl)phenyl]benzamide Chemical compound CCC(C)(C)CC(C)C1=CC=CC=C1NC(=O)C1=CC=CC=C1Cl AKPLYNMWGYVIRE-UHFFFAOYSA-N 0.000 description 2
- CAAMSDWKXXPUJR-UHFFFAOYSA-N 3,5-dihydro-4H-imidazol-4-one Chemical class O=C1CNC=N1 CAAMSDWKXXPUJR-UHFFFAOYSA-N 0.000 description 2
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- BQMRHYBXRAYYQS-UHFFFAOYSA-N 4-dihydroxyphosphinothioyloxy-n,n-diethyl-6-methylpyrimidin-2-amine Chemical compound CCN(CC)C1=NC(C)=CC(OP(O)(O)=S)=N1 BQMRHYBXRAYYQS-UHFFFAOYSA-N 0.000 description 2
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- CJJOSEISRRTUQB-UHFFFAOYSA-N azinphos-methyl Chemical compound C1=CC=C2C(=O)N(CSP(=S)(OC)OC)N=NC2=C1 CJJOSEISRRTUQB-UHFFFAOYSA-N 0.000 description 2
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- ARUVKPQLZAKDPS-UHFFFAOYSA-L copper(II) sulfate Chemical compound [Cu+2].[O-][S+2]([O-])([O-])[O-] ARUVKPQLZAKDPS-UHFFFAOYSA-L 0.000 description 2
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- HSMVPDGQOIQYSR-KGENOOAVSA-N triflumizole Chemical compound C1=CN=CN1C(/COCCC)=N/C1=CC=C(Cl)C=C1C(F)(F)F HSMVPDGQOIQYSR-KGENOOAVSA-N 0.000 description 1
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- LESVOLZBIFDZGS-UHFFFAOYSA-N vamidothion Chemical compound CNC(=O)C(C)SCCSP(=O)(OC)OC LESVOLZBIFDZGS-UHFFFAOYSA-N 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 230000017260 vegetative to reproductive phase transition of meristem Effects 0.000 description 1
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- 235000020234 walnut Nutrition 0.000 description 1
- 239000005943 zeta-Cypermethrin Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 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
- FJBGIXKIXPUXBY-UHFFFAOYSA-N {2-[3-(4-chlorophenyl)propyl]-2,4,4-trimethyl-1,3-oxazolidin-3-yl}(imidazol-1-yl)methanone Chemical compound C1=CN=CN1C(=O)N1C(C)(C)COC1(C)CCCC1=CC=C(Cl)C=C1 FJBGIXKIXPUXBY-UHFFFAOYSA-N 0.000 description 1
- JLYXXMFPNIAWKQ-UHFFFAOYSA-N γ Benzene hexachloride Chemical compound ClC1C(Cl)C(Cl)C(Cl)C(Cl)C1Cl JLYXXMFPNIAWKQ-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C211/00—Compounds containing amino groups bound to a carbon skeleton
- C07C211/43—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton
- C07C211/44—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton having amino groups bound to only one six-membered aromatic ring
- C07C211/45—Monoamines
- C07C211/48—N-alkylated amines
-
- 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof
- A01N37/22—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof the nitrogen atom being directly attached to an aromatic ring system, e.g. anilides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C233/00—Carboxylic acid amides
- C07C233/64—Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings
- C07C233/65—Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atoms of the carboxamide groups bound to hydrogen atoms or to carbon atoms of unsubstituted hydrocarbon radicals
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Agronomy & Crop Science (AREA)
- General Health & Medical Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10229595A DE10229595A1 (de) | 2002-07-02 | 2002-07-02 | Phenylbenzamide |
| PCT/EP2003/006512 WO2004005242A1 (de) | 2002-07-02 | 2003-06-20 | Phenylbenzamide |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MXPA05000114A true MXPA05000114A (es) | 2005-04-08 |
Family
ID=29723619
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MXPA05000114A MXPA05000114A (es) | 2002-07-02 | 2003-06-20 | Fenilbenzamidas. |
Country Status (18)
| Country | Link |
|---|---|
| US (1) | US7314958B2 (https=) |
| EP (1) | EP1519913A1 (https=) |
| JP (1) | JP4520299B2 (https=) |
| KR (1) | KR101025742B1 (https=) |
| CN (1) | CN1324005C (https=) |
| AR (1) | AR039743A1 (https=) |
| AU (1) | AU2003245975A1 (https=) |
| BR (1) | BR0312407B1 (https=) |
| CA (1) | CA2491368A1 (https=) |
| DE (1) | DE10229595A1 (https=) |
| EA (1) | EA009884B1 (https=) |
| IL (1) | IL165925A (https=) |
| MX (1) | MXPA05000114A (https=) |
| PL (1) | PL374466A1 (https=) |
| TW (1) | TW200413284A (https=) |
| UA (1) | UA78340C2 (https=) |
| WO (1) | WO2004005242A1 (https=) |
| ZA (1) | ZA200500014B (https=) |
Families Citing this family (31)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE10349501A1 (de) * | 2003-10-23 | 2005-05-25 | Bayer Cropscience Ag | Synergistische fungizide Wirkstoffkombinationen |
| DE10354607A1 (de) | 2003-11-21 | 2005-06-16 | Bayer Cropscience Ag | Siylierte Carboxamide |
| DE102004005317A1 (de) * | 2003-12-18 | 2005-07-21 | Bayer Cropscience Ag | Optisch aktive Carboxamide |
| EP1697329A1 (de) * | 2003-12-18 | 2006-09-06 | Bayer CropScience Aktiengesellschaft | Optisch aktive carboxamide und deren verwendung zur bekämpfung von unerwünschten mikroorganismen |
| DE102004005785A1 (de) * | 2004-02-06 | 2005-08-25 | Bayer Cropscience Ag | 2-Halogenfuryl/thienyl-3-carboxamide |
| DE102004005786A1 (de) * | 2004-02-06 | 2005-08-25 | Bayer Cropscience Ag | Haloalkylcarboxamide |
| DE102004029972A1 (de) * | 2004-06-21 | 2006-01-05 | Bayer Cropscience Ag | Beizmittel zur Bekämpfung von phytopathogenen Pilzen |
| DE102005015850A1 (de) | 2005-04-07 | 2006-10-12 | Bayer Cropscience Ag | Synergistische fungizide Wirkstoffkombinationen |
| UA89673C2 (ru) * | 2005-04-28 | 2010-02-25 | Байер Кропсайенс Аг | Комбинация активных веществ для борьбы с нежелательными вредителями животных |
| DE102005022147A1 (de) * | 2005-04-28 | 2006-11-02 | Bayer Cropscience Ag | Wirkstoffkombinationen |
| DE102005026482A1 (de) | 2005-06-09 | 2006-12-14 | Bayer Cropscience Ag | Wirkstoffkombinationen |
| CN104170838B (zh) | 2005-06-09 | 2016-03-30 | 拜尔农作物科学股份公司 | 活性物质结合物 |
| DE102005035300A1 (de) | 2005-07-28 | 2007-02-01 | Bayer Cropscience Ag | Synergistische fungizide Wirkstoffkombinationen |
| DE102006023263A1 (de) * | 2006-05-18 | 2007-11-22 | Bayer Cropscience Ag | Synergistische Wirkstoffkombinationen |
| JP2010518179A (ja) * | 2007-02-14 | 2010-05-27 | ビーエーエスエフ ソシエタス・ヨーロピア | 植物のウイルス耐性誘発方法 |
| US8236988B2 (en) | 2007-08-30 | 2012-08-07 | Albemarle Corporation | Preparation of 2-(1,3-dimethylbutyl)aniline and other branched alkyl-substituted-anilines |
| DE102007045920B4 (de) | 2007-09-26 | 2018-07-05 | Bayer Intellectual Property Gmbh | Synergistische Wirkstoffkombinationen |
| EP4410100A3 (en) | 2008-02-05 | 2024-10-09 | Basf Se | Plant health composition |
| EA019439B1 (ru) * | 2008-10-21 | 2014-03-31 | Басф Се | Применение карбоксамидов на культивируемых растениях |
| WO2010108507A2 (de) | 2009-03-25 | 2010-09-30 | Bayer Cropscience Ag | Synergistische wirkstoffkombinationen |
| CN102510721B (zh) | 2009-07-16 | 2014-11-19 | 拜尔农作物科学股份公司 | 含苯基三唑的协同活性物质结合物 |
| MX2012006437A (es) | 2009-12-08 | 2012-07-04 | Basf Se | Mezclas de plaguicidas. |
| PL2509417T3 (pl) | 2009-12-08 | 2017-09-29 | Basf Se | Mieszaniny pestycydowe |
| JP5782116B2 (ja) | 2010-05-28 | 2015-09-24 | ビーエーエスエフ ソシエタス・ヨーロピアＢａｓｆ Ｓｅ | 殺有害生物混合物 |
| US8551746B2 (en) * | 2011-09-21 | 2013-10-08 | Coskata, Inc. | Method for controlling undesirable byproducts formation caused by contaminating organisms in the production of ethanol from syngas |
| US20170015871A1 (en) | 2013-11-29 | 2017-01-19 | Proionic Gmbh | Method for curing an adhesive using microwave irradiation |
| EP2910126A1 (en) | 2015-05-05 | 2015-08-26 | Bayer CropScience AG | Active compound combinations having insecticidal properties |
| AU2017342206B2 (en) | 2016-10-14 | 2022-06-02 | Pi Industries Ltd | 4-amino substituted phenylamidine derivatives and their use to protect crops by fighting undesired phytopathogenic micoorganisms |
| EP3525588B1 (en) | 2016-10-14 | 2024-04-24 | PI Industries Ltd | 4-substituted phenylamidine derivatives and their use to protect crops by fighting undesired phytopathogenic micoorganisms |
| CN116918810B (zh) * | 2022-06-22 | 2026-01-30 | 河北艾林化工科技有限公司 | 一种杀虫剂组合物及其应用 |
| CN118985618B (zh) * | 2024-07-05 | 2025-10-10 | 云南大学 | 一种苯甲酰胺类化合物在防治植物根结线虫中的应用 |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2730620A1 (de) | 1977-07-07 | 1979-01-25 | Bayer Ag | Neue n-aryl-n'-alkyl-s-alkyl- isothioharnstoffe, verfahren zu ihrer herstellung sowie ihre verwendung als mittel zur bekaempfung von tierischen und pflanzlichen schaedlingen |
| JPS58140054A (ja) * | 1982-02-10 | 1983-08-19 | Sumitomo Chem Co Ltd | インダニルベンツアミド誘導体、その製造法およびこれらを有効成分として含有する農園芸用殺菌剤 |
| IL103614A (en) | 1991-11-22 | 1998-09-24 | Basf Ag | Carboxamides for controlling botrytis and certain novel such compounds |
| DE19629828A1 (de) * | 1996-07-24 | 1998-01-29 | Bayer Ag | Carbanilide |
| US5914344A (en) * | 1996-08-15 | 1999-06-22 | Mitsui Chemicals, Inc. | Substituted carboxanilide derivative and plant disease control agent comprising same as active ingredient |
| JP2001072510A (ja) * | 1999-09-03 | 2001-03-21 | Mitsui Chemicals Inc | 植物病害防除剤組成物 |
| JP2001072508A (ja) * | 1999-09-03 | 2001-03-21 | Mitsui Chemicals Inc | 植物病害防除剤組成物 |
| ES2271109T3 (es) * | 2000-11-08 | 2007-04-16 | Syngenta Participations Ag | Pirrocarboxamidas y pirrolcarbotioamidas y sus usos agroquimicos. |
| DE10136065A1 (de) * | 2001-07-25 | 2003-02-13 | Bayer Cropscience Ag | Pyrazolylcarboxanilide |
-
2002
- 2002-07-02 DE DE10229595A patent/DE10229595A1/de not_active Withdrawn
-
2003
- 2003-06-20 EA EA200500037A patent/EA009884B1/ru not_active IP Right Cessation
- 2003-06-20 EP EP03738073A patent/EP1519913A1/de not_active Withdrawn
- 2003-06-20 KR KR1020047021497A patent/KR101025742B1/ko not_active Expired - Fee Related
- 2003-06-20 US US10/518,446 patent/US7314958B2/en not_active Expired - Fee Related
- 2003-06-20 WO PCT/EP2003/006512 patent/WO2004005242A1/de not_active Ceased
- 2003-06-20 UA UAA200500915A patent/UA78340C2/uk unknown
- 2003-06-20 BR BRPI0312407-0A patent/BR0312407B1/pt not_active IP Right Cessation
- 2003-06-20 CA CA002491368A patent/CA2491368A1/en not_active Abandoned
- 2003-06-20 AU AU2003245975A patent/AU2003245975A1/en not_active Abandoned
- 2003-06-20 JP JP2004518548A patent/JP4520299B2/ja not_active Expired - Fee Related
- 2003-06-20 CN CNB038208121A patent/CN1324005C/zh not_active Expired - Fee Related
- 2003-06-20 MX MXPA05000114A patent/MXPA05000114A/es active IP Right Grant
- 2003-06-20 PL PL03374466A patent/PL374466A1/xx not_active Application Discontinuation
- 2003-06-25 AR ARP030102277A patent/AR039743A1/es unknown
- 2003-07-01 TW TW092117901A patent/TW200413284A/zh unknown
-
2004
- 2004-12-22 IL IL165925A patent/IL165925A/en not_active IP Right Cessation
-
2005
- 2005-01-03 ZA ZA200500014A patent/ZA200500014B/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| AU2003245975A1 (en) | 2004-01-23 |
| CN1678567A (zh) | 2005-10-05 |
| EA200500037A1 (ru) | 2005-06-30 |
| JP2006503809A (ja) | 2006-02-02 |
| AR039743A1 (es) | 2005-03-09 |
| US20060211771A1 (en) | 2006-09-21 |
| KR20050016657A (ko) | 2005-02-21 |
| CN1324005C (zh) | 2007-07-04 |
| IL165925A (en) | 2009-12-24 |
| US7314958B2 (en) | 2008-01-01 |
| WO2004005242A1 (de) | 2004-01-15 |
| ZA200500014B (en) | 2006-06-28 |
| PL374466A1 (en) | 2005-10-31 |
| TW200413284A (en) | 2004-08-01 |
| BR0312407A (pt) | 2005-04-26 |
| JP4520299B2 (ja) | 2010-08-04 |
| EA009884B1 (ru) | 2008-04-28 |
| IL165925A0 (en) | 2006-01-15 |
| CA2491368A1 (en) | 2004-01-15 |
| EP1519913A1 (de) | 2005-04-06 |
| BR0312407B1 (pt) | 2014-03-25 |
| DE10229595A1 (de) | 2004-01-15 |
| UA78340C2 (en) | 2007-03-15 |
| KR101025742B1 (ko) | 2011-04-04 |
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