DE10229595A1 - Phenylbenzamide - Google Patents
Phenylbenzamide Download PDFInfo
- Publication number
- DE10229595A1 DE10229595A1 DE10229595A DE10229595A DE10229595A1 DE 10229595 A1 DE10229595 A1 DE 10229595A1 DE 10229595 A DE10229595 A DE 10229595A DE 10229595 A DE10229595 A DE 10229595A DE 10229595 A1 DE10229595 A1 DE 10229595A1
- Authority
- DE
- Germany
- Prior art keywords
- formula
- phenyl
- plants
- methyl
- phenylbenzamides
- Prior art date
- Legal status (The legal status 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 status listed.)
- Withdrawn
Links
- GTKIGDZXPDCIKR-UHFFFAOYSA-N 2-phenylbenzamide Chemical class NC(=O)C1=CC=CC=C1C1=CC=CC=C1 GTKIGDZXPDCIKR-UHFFFAOYSA-N 0.000 title claims abstract description 22
- 238000000034 method Methods 0.000 claims abstract description 29
- 238000002360 preparation method Methods 0.000 claims abstract description 27
- 244000005700 microbiome Species 0.000 claims abstract description 18
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 14
- 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
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims abstract description 10
- 230000008569 process Effects 0.000 claims abstract description 8
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims abstract description 5
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims abstract description 5
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims abstract description 5
- 229910052794 bromium Inorganic materials 0.000 claims abstract description 5
- 239000000460 chlorine Substances 0.000 claims abstract description 5
- 229910052801 chlorine Inorganic materials 0.000 claims abstract description 5
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims abstract description 4
- 239000011630 iodine Substances 0.000 claims abstract description 4
- 229910052740 iodine Inorganic materials 0.000 claims abstract description 4
- -1 1,3-dimethylbutyl Chemical group 0.000 claims description 31
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 claims description 19
- 239000004606 Fillers/Extenders Substances 0.000 claims description 5
- PASDCCFISLVPSO-UHFFFAOYSA-N benzoyl chloride Chemical compound ClC(=O)C1=CC=CC=C1 PASDCCFISLVPSO-UHFFFAOYSA-N 0.000 claims description 5
- 239000002841 Lewis acid Substances 0.000 claims description 4
- 239000002253 acid Substances 0.000 claims description 4
- 150000001336 alkenes Chemical class 0.000 claims description 4
- 150000007517 lewis acids Chemical class 0.000 claims description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 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
- 239000011230 binding agent Substances 0.000 claims description 3
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- 239000003085 diluting agent Substances 0.000 claims description 3
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 claims description 3
- 239000004094 surface-active agent Substances 0.000 claims description 2
- 239000013543 active substance Substances 0.000 claims 1
- 150000001448 anilines Chemical class 0.000 claims 1
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- 238000004519 manufacturing process Methods 0.000 abstract description 4
- 239000000543 intermediate Substances 0.000 abstract description 2
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- 239000004480 active ingredient Substances 0.000 description 37
- 238000012360 testing method Methods 0.000 description 24
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- 150000001875 compounds Chemical class 0.000 description 19
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- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 17
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- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 15
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 15
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- 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 6
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- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 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
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 6
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- 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
- 241000223600 Alternaria Species 0.000 description 4
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- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 4
- 244000070406 Malus silvestris Species 0.000 description 4
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 4
- 244000061456 Solanum tuberosum Species 0.000 description 4
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- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- NZCKTGCKFJDGFD-UHFFFAOYSA-N 2-bromobenzoyl chloride Chemical compound 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
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- DPOWHSMECVNHAT-YERPJTIDSA-N tetcyclacis Chemical compound C1=CC(Cl)=CC=C1N1[C@H]2[C@H]([C@@H]3[C@H]4N=N3)C[C@H]4[C@H]2N=N1 DPOWHSMECVNHAT-YERPJTIDSA-N 0.000 description 1
- UBCKGWBNUIFUST-YHYXMXQVSA-N tetrachlorvinphos Chemical compound COP(=O)(OC)O\C(=C/Cl)C1=CC(Cl)=C(Cl)C=C1Cl UBCKGWBNUIFUST-YHYXMXQVSA-N 0.000 description 1
- MLGCXEBRWGEOQX-UHFFFAOYSA-N tetradifon Chemical compound C1=CC(Cl)=CC=C1S(=O)(=O)C1=CC(Cl)=C(Cl)C=C1Cl MLGCXEBRWGEOQX-UHFFFAOYSA-N 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 239000004308 thiabendazole Substances 0.000 description 1
- 235000010296 thiabendazole Nutrition 0.000 description 1
- WJCNZQLZVWNLKY-UHFFFAOYSA-N thiabendazole Chemical compound S1C=NC(C=2NC3=CC=CC=C3N=2)=C1 WJCNZQLZVWNLKY-UHFFFAOYSA-N 0.000 description 1
- 229960004546 thiabendazole Drugs 0.000 description 1
- NWWZPOKUUAIXIW-FLIBITNWSA-N thiamethoxam Chemical compound [O-][N+](=O)\N=C/1N(C)COCN\1CC1=CN=C(Cl)S1 NWWZPOKUUAIXIW-FLIBITNWSA-N 0.000 description 1
- WOSNCVAPUOFXEH-UHFFFAOYSA-N thifluzamide Chemical compound S1C(C)=NC(C(F)(F)F)=C1C(=O)NC1=C(Br)C=C(OC(F)(F)F)C=C1Br WOSNCVAPUOFXEH-UHFFFAOYSA-N 0.000 description 1
- DNVLJEWNNDHELH-UHFFFAOYSA-N thiocyclam Chemical compound CN(C)C1CSSSC1 DNVLJEWNNDHELH-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
- QGHREAKMXXNCOA-UHFFFAOYSA-N thiophanate-methyl Chemical compound COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC QGHREAKMXXNCOA-UHFFFAOYSA-N 0.000 description 1
- 229960002447 thiram Drugs 0.000 description 1
- KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 description 1
- 229940074152 thuringiensin Drugs 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- OBZIQQJJIKNWNO-UHFFFAOYSA-N tolclofos-methyl Chemical compound COP(=S)(OC)OC1=C(Cl)C=C(C)C=C1Cl OBZIQQJJIKNWNO-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
- 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 description 1
- 238000012546 transfer Methods 0.000 description 1
- BAZVSMNPJJMILC-UHFFFAOYSA-N triadimenol Chemical compound C1=NC=NN1C(C(O)C(C)(C)C)OC1=CC=C(Cl)C=C1 BAZVSMNPJJMILC-UHFFFAOYSA-N 0.000 description 1
- JWXZLCFGVKMEEK-UHFFFAOYSA-N triarathene Chemical compound C1=CC(Cl)=CC=C1C1=CC(C=2C=CC=CC=2)=C(C=2C=CC=CC=2)S1 JWXZLCFGVKMEEK-UHFFFAOYSA-N 0.000 description 1
- NKNFWVNSBIXGLL-UHFFFAOYSA-N triazamate Chemical compound CCOC(=O)CSC1=NC(C(C)(C)C)=NN1C(=O)N(C)C NKNFWVNSBIXGLL-UHFFFAOYSA-N 0.000 description 1
- AMFGTOFWMRQMEM-UHFFFAOYSA-N triazophos Chemical compound N1=C(OP(=S)(OCC)OCC)N=CN1C1=CC=CC=C1 AMFGTOFWMRQMEM-UHFFFAOYSA-N 0.000 description 1
- IQGKIPDJXCAMSM-UHFFFAOYSA-N triazoxide Chemical compound N=1C2=CC=C(Cl)C=C2[N+]([O-])=NC=1N1C=CN=C1 IQGKIPDJXCAMSM-UHFFFAOYSA-N 0.000 description 1
- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
- NFACJZMKEDPNKN-UHFFFAOYSA-N trichlorfon Chemical compound COP(=O)(OC)C(O)C(Cl)(Cl)Cl NFACJZMKEDPNKN-UHFFFAOYSA-N 0.000 description 1
- DQJCHOQLCLEDLL-UHFFFAOYSA-N tricyclazole Chemical compound CC1=CC=CC2=C1N1C=NN=C1S2 DQJCHOQLCLEDLL-UHFFFAOYSA-N 0.000 description 1
- ONCZDRURRATYFI-TVJDWZFNSA-N trifloxystrobin Chemical compound CO\N=C(\C(=O)OC)C1=CC=CC=C1CO\N=C(/C)C1=CC=CC(C(F)(F)F)=C1 ONCZDRURRATYFI-TVJDWZFNSA-N 0.000 description 1
- 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
- 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 description 1
- RROQIUMZODEXOR-UHFFFAOYSA-N triforine Chemical compound O=CNC(C(Cl)(Cl)Cl)N1CCN(C(NC=O)C(Cl)(Cl)Cl)CC1 RROQIUMZODEXOR-UHFFFAOYSA-N 0.000 description 1
- 241000701447 unidentified baculovirus Species 0.000 description 1
- JARYYMUOCXVXNK-CSLFJTBJSA-N validamycin A Chemical compound N([C@H]1C[C@@H]([C@H]([C@H](O)[C@H]1O)O[C@H]1[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O1)O)CO)[C@H]1C=C(CO)[C@@H](O)[C@H](O)[C@H]1O JARYYMUOCXVXNK-CSLFJTBJSA-N 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- PXXNTAGJWPJAGM-UHFFFAOYSA-N vertaline Natural products C1C2C=3C=C(OC)C(OC)=CC=3OC(C=C3)=CC=C3CCC(=O)OC1CC1N2CCCC1 PXXNTAGJWPJAGM-UHFFFAOYSA-N 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)
Priority Applications (18)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10229595A DE10229595A1 (de) | 2002-07-02 | 2002-07-02 | Phenylbenzamide |
| EP03738073A EP1519913A1 (de) | 2002-07-02 | 2003-06-20 | Phenylbenzamide |
| JP2004518548A JP4520299B2 (ja) | 2002-07-02 | 2003-06-20 | フェニルベンズアミド |
| CA002491368A CA2491368A1 (en) | 2002-07-02 | 2003-06-20 | Phenyl benzamides |
| PCT/EP2003/006512 WO2004005242A1 (de) | 2002-07-02 | 2003-06-20 | Phenylbenzamide |
| AU2003245975A AU2003245975A1 (en) | 2002-07-02 | 2003-06-20 | Phenyl benzamides |
| BRPI0312407-0A BR0312407B1 (pt) | 2002-07-02 | 2003-06-20 | Fenilbenzamidas, seu emprego e seu processo de preparação, processo e composição para combate de microorganismos indesejados, processo para preparação da dita composição, e processo para preparação de derivados de alquilfenilamina |
| CNB038208121A CN1324005C (zh) | 2002-07-02 | 2003-06-20 | 苯基苯酰胺 |
| US10/518,446 US7314958B2 (en) | 2002-07-02 | 2003-06-20 | Phenylbenzamides |
| KR1020047021497A KR101025742B1 (ko) | 2002-07-02 | 2003-06-20 | 페닐 벤즈아미드 |
| PL03374466A PL374466A1 (en) | 2002-07-02 | 2003-06-20 | Phenyl benzamides |
| UAA200500915A UA78340C2 (en) | 2002-07-02 | 2003-06-20 | Phenyl benzamides and agent for controlling undesired microorganisms based thereon |
| EA200500037A EA009884B1 (ru) | 2002-07-02 | 2003-06-20 | Фенилбензамиды |
| MXPA05000114A MXPA05000114A (es) | 2002-07-02 | 2003-06-20 | Fenilbenzamidas. |
| ARP030102277A AR039743A1 (es) | 2002-07-02 | 2003-06-25 | Fenilbenzamidas y su uso para el control de microoganismos indeseados |
| TW092117901A TW200413284A (en) | 2002-07-02 | 2003-07-01 | Phenylbenzamides |
| IL165925A IL165925A (en) | 2002-07-02 | 2004-12-22 | Phenyl benzamides, processes for their preparation, compositions comprising them and uses thereof |
| ZA200500014A ZA200500014B (en) | 2002-07-02 | 2005-01-03 | Phenyl benzamides |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10229595A DE10229595A1 (de) | 2002-07-02 | 2002-07-02 | Phenylbenzamide |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE10229595A1 true DE10229595A1 (de) | 2004-01-15 |
Family
ID=29723619
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE10229595A Withdrawn DE10229595A1 (de) | 2002-07-02 | 2002-07-02 | Phenylbenzamide |
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=) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2213168A1 (de) | 2005-04-28 | 2010-08-04 | Bayer CropScience AG | Pestizide Wirkstoffkombinationen |
| EP2356905A1 (de) | 2003-10-23 | 2011-08-17 | Bayer Cropscience AG | Synergistische fungizide Wirkstoffkombinationen |
Families Citing this family (29)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| 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 |
| KR20060126713A (ko) * | 2003-12-18 | 2006-12-08 | 바이엘 크롭사이언스 아게 | 광학적 활성 카복사미드 및 원치않는 미생물을 구제하기위한 그의 용도 |
| DE102004005786A1 (de) * | 2004-02-06 | 2005-08-25 | Bayer Cropscience Ag | Haloalkylcarboxamide |
| DE102004005785A1 (de) * | 2004-02-06 | 2005-08-25 | Bayer Cropscience Ag | 2-Halogenfuryl/thienyl-3-carboxamide |
| 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 |
| CN101203135B (zh) * | 2005-04-28 | 2014-06-11 | 拜尔农作物科学股份公司 | 农药活性物质结合物 |
| DE102005026482A1 (de) | 2005-06-09 | 2006-12-14 | Bayer Cropscience Ag | Wirkstoffkombinationen |
| EA201270781A1 (ru) | 2005-06-09 | 2013-09-30 | Байер Кропсайенс Аг | Комбинации биологически активных веществ |
| 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 |
| EP2109362A2 (en) * | 2007-02-14 | 2009-10-21 | Basf Se | Method of inducing virus tolerance of plants |
| ATE528278T1 (de) | 2007-08-30 | 2011-10-15 | Albemarle Corp | Herstellung von 2-(1,3-dimethylbutyl)anilin und anderen verzweigten, alkylsubstituierten anilinen |
| DE102007045920B4 (de) | 2007-09-26 | 2018-07-05 | Bayer Intellectual Property Gmbh | Synergistische Wirkstoffkombinationen |
| JP2011511033A (ja) | 2008-02-05 | 2011-04-07 | ビーエーエスエフ ソシエタス・ヨーロピア | 植物体健康組成物 |
| EA023545B1 (ru) * | 2008-10-21 | 2016-06-30 | Басф Се | Применение карбоксамида флуопирама на культивируемых растениях |
| MX2011009732A (es) | 2009-03-25 | 2011-09-29 | Bayer Cropscience Ag | Combinaciones de principios activos sinergicas. |
| KR20120051015A (ko) | 2009-07-16 | 2012-05-21 | 바이엘 크롭사이언스 아게 | 페닐 트리아졸을 함유하는 상승적 활성 물질 배합물 |
| US8748342B2 (en) | 2009-12-08 | 2014-06-10 | Basf Se | Pesticidal mixtures |
| NZ600886A (en) | 2009-12-08 | 2013-06-28 | Basf Se | An agrochemical pesticidal mixture for increasing the yield and health of a plant |
| ES2567266T3 (es) | 2010-05-28 | 2016-04-21 | Basf Se | Mezclas de pesticidas |
| 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 |
| KR102339016B1 (ko) | 2013-11-29 | 2021-12-14 | 프로이오닉 게엠베하 | 마이크로파 조사에 의한 접착제 경화 방법 |
| EP2910126A1 (en) | 2015-05-05 | 2015-08-26 | Bayer CropScience AG | Active compound combinations having insecticidal properties |
| WO2018069841A1 (en) | 2016-10-14 | 2018-04-19 | Pi Industries Ltd | 4-substituted phenylamine derivatives and their use to protect crops by fighting undesired phytopathogenic micoorganisms |
| CA3040408A1 (en) | 2016-10-14 | 2018-04-19 | Pi Industries Ltd | 4-amino 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 |
| JP3982879B2 (ja) * | 1996-08-15 | 2007-09-26 | 三井化学株式会社 | 置換カルボン酸アニリド誘導体およびこれを有効成分とする植物病害防除剤 |
| JP2001072508A (ja) * | 1999-09-03 | 2001-03-21 | Mitsui Chemicals Inc | 植物病害防除剤組成物 |
| JP2001072510A (ja) * | 1999-09-03 | 2001-03-21 | Mitsui Chemicals Inc | 植物病害防除剤組成物 |
| US7105565B2 (en) * | 2000-11-08 | 2006-09-12 | Syngenta Crop Protection, Inc. | Pyrrolcarboxamides and pyrrolcarbothioamides and their agrochemical uses |
| 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 JP JP2004518548A patent/JP4520299B2/ja not_active Expired - Fee Related
- 2003-06-20 US US10/518,446 patent/US7314958B2/en not_active Expired - Fee Related
- 2003-06-20 PL PL03374466A patent/PL374466A1/xx not_active Application Discontinuation
- 2003-06-20 KR KR1020047021497A patent/KR101025742B1/ko not_active Expired - Fee Related
- 2003-06-20 EA EA200500037A patent/EA009884B1/ru not_active IP Right Cessation
- 2003-06-20 BR BRPI0312407-0A patent/BR0312407B1/pt not_active IP Right Cessation
- 2003-06-20 CN CNB038208121A patent/CN1324005C/zh not_active Expired - Fee Related
- 2003-06-20 EP EP03738073A patent/EP1519913A1/de not_active Withdrawn
- 2003-06-20 MX MXPA05000114A patent/MXPA05000114A/es active IP Right Grant
- 2003-06-20 UA UAA200500915A patent/UA78340C2/uk unknown
- 2003-06-20 AU AU2003245975A patent/AU2003245975A1/en not_active Abandoned
- 2003-06-20 CA CA002491368A patent/CA2491368A1/en not_active Abandoned
- 2003-06-20 WO PCT/EP2003/006512 patent/WO2004005242A1/de not_active Ceased
- 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
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2356905A1 (de) | 2003-10-23 | 2011-08-17 | Bayer Cropscience AG | Synergistische fungizide Wirkstoffkombinationen |
| EP2356906A1 (de) | 2003-10-23 | 2011-08-17 | Bayer Cropscience AG | Synergistische fungizide Wirkstoffkombinationen |
| EP2364592A1 (de) | 2003-10-23 | 2011-09-14 | Bayer Cropscience AG | Synergistische fungizide Wirkstoffkombinationen |
| EP2796043A1 (de) | 2003-10-23 | 2014-10-29 | Bayer CropScience AG | Synergistische fungizide Wirkstoffkombinationen |
| EP2213168A1 (de) | 2005-04-28 | 2010-08-04 | Bayer CropScience AG | Pestizide Wirkstoffkombinationen |
Also Published As
| Publication number | Publication date |
|---|---|
| CN1678567A (zh) | 2005-10-05 |
| AU2003245975A1 (en) | 2004-01-23 |
| EP1519913A1 (de) | 2005-04-06 |
| MXPA05000114A (es) | 2005-04-08 |
| BR0312407B1 (pt) | 2014-03-25 |
| KR20050016657A (ko) | 2005-02-21 |
| IL165925A0 (en) | 2006-01-15 |
| UA78340C2 (en) | 2007-03-15 |
| CA2491368A1 (en) | 2004-01-15 |
| US20060211771A1 (en) | 2006-09-21 |
| WO2004005242A1 (de) | 2004-01-15 |
| JP4520299B2 (ja) | 2010-08-04 |
| CN1324005C (zh) | 2007-07-04 |
| EA200500037A1 (ru) | 2005-06-30 |
| AR039743A1 (es) | 2005-03-09 |
| US7314958B2 (en) | 2008-01-01 |
| JP2006503809A (ja) | 2006-02-02 |
| IL165925A (en) | 2009-12-24 |
| KR101025742B1 (ko) | 2011-04-04 |
| ZA200500014B (en) | 2006-06-28 |
| EA009884B1 (ru) | 2008-04-28 |
| BR0312407A (pt) | 2005-04-26 |
| TW200413284A (en) | 2004-08-01 |
| PL374466A1 (en) | 2005-10-31 |
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| Date | Code | Title | Description |
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| 8139 | Disposal/non-payment of the annual fee |