UA78340C2 - Phenyl benzamides and agent for controlling undesired microorganisms based thereon - Google Patents

Phenyl benzamides and agent for controlling undesired microorganisms based thereon Download PDF

Info

Publication number: UA78340C2
Authority: UA; Ukraine
Prior art keywords: plants; phenyl; species; formula; methyl
Prior art date: 2002-07-02

Application number

UAA200500915A

Other languages

English (en)

Ukrainian (uk)

Original Assignee

Bayer Cropscience 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.)

2002-07-02

Filing date

2003-06-20

Publication date

2007-03-15

2003-06-20 Application filed by Bayer Cropscience Ag filed Critical Bayer Cropscience Ag

2007-03-15 Publication of UA78340C2 publication Critical patent/UA78340C2/uk

Links

244000005700 microbiome Species 0.000 title claims abstract description 17
ZVSKZLHKADLHSD-UHFFFAOYSA-N benzanilide Chemical class C=1C=CC=CC=1C(=O)NC1=CC=CC=C1 ZVSKZLHKADLHSD-UHFFFAOYSA-N 0.000 title abstract 2
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims abstract description 10
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 9
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims abstract description 7
239000001257 hydrogen Substances 0.000 claims abstract description 7
229910052739 hydrogen Inorganic materials 0.000 claims abstract description 7
229910052740 iodine Chemical group 0.000 claims abstract description 5
ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims abstract description 4
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical group [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims abstract description 4
229910052794 bromium Inorganic materials 0.000 claims abstract description 4
239000000460 chlorine Chemical group 0.000 claims abstract description 4
229910052801 chlorine Inorganic materials 0.000 claims abstract description 4
239000011630 iodine Chemical group 0.000 claims abstract description 4
239000013543 active substance Substances 0.000 claims description 58
KXDAEFPNCMNJSK-UHFFFAOYSA-N Benzamide Chemical compound NC(=O)C1=CC=CC=C1 KXDAEFPNCMNJSK-UHFFFAOYSA-N 0.000 claims description 34
GTKIGDZXPDCIKR-UHFFFAOYSA-N 2-phenylbenzamide Chemical class NC(=O)C1=CC=CC=C1C1=CC=CC=C1 GTKIGDZXPDCIKR-UHFFFAOYSA-N 0.000 claims description 17
239000003085 diluting agent Substances 0.000 claims description 6
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 5
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 5
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 3
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 3
150000002431 hydrogen Chemical class 0.000 claims 1
239000000126 substance Substances 0.000 abstract description 15
238000004519 manufacturing process Methods 0.000 abstract description 3
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 81
-1 M-(2-hexylphenyl)-2-iodobenzamide Chemical compound 0.000 description 48
241000894007 species Species 0.000 description 35
239000000203 mixture Substances 0.000 description 27
238000000034 method Methods 0.000 description 24
230000009471 action Effects 0.000 description 22
230000001681 protective effect Effects 0.000 description 22
WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 18
150000001875 compounds Chemical class 0.000 description 16
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-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
239000000463 material Substances 0.000 description 15
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 15
238000011160 research Methods 0.000 description 13
239000002904 solvent Substances 0.000 description 13
PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 12
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 12
240000008042 Zea mays Species 0.000 description 10
235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 10
235000002017 Zea mays subsp mays 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
241000700605 Viruses Species 0.000 description 9
238000006243 chemical reaction Methods 0.000 description 9
238000012545 processing Methods 0.000 description 9
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241000233866 Fungi Species 0.000 description 8
244000299507 Gossypium hirsutum Species 0.000 description 8
241000607479 Yersinia pestis Species 0.000 description 8
ZMXDDKWLCZADIW-UHFFFAOYSA-N dimethylformamide Substances CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 8
WSSSPWUEQFSQQG-UHFFFAOYSA-N 4-methyl-1-pentene Chemical compound CC(C)CC=C WSSSPWUEQFSQQG-UHFFFAOYSA-N 0.000 description 6
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
244000068988 Glycine max Species 0.000 description 6
235000010469 Glycine max Nutrition 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
208000015181 infectious disease Diseases 0.000 description 6
229920000151 polyglycol Polymers 0.000 description 6
239000010695 polyglycol Substances 0.000 description 6
241000894006 Bacteria Species 0.000 description 5
RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 5
XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 5
150000003857 carboxamides Chemical class 0.000 description 5
239000010949 copper Substances 0.000 description 5
229910052802 copper Inorganic materials 0.000 description 5
239000008187 granular material Substances 0.000 description 5
239000012074 organic phase Substances 0.000 description 5
229910000027 potassium carbonate Inorganic materials 0.000 description 5
235000011181 potassium carbonates Nutrition 0.000 description 5
238000002360 preparation method Methods 0.000 description 5
239000011541 reaction mixture Substances 0.000 description 5
239000002689 soil Substances 0.000 description 5
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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
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 4
240000005979 Hordeum vulgare Species 0.000 description 4
244000070406 Malus silvestris Species 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
125000002877 alkyl aryl group Chemical group 0.000 description 4
239000002585 base Substances 0.000 description 4
238000004587 chromatography analysis Methods 0.000 description 4
239000000417 fungicide Substances 0.000 description 4
238000011534 incubation Methods 0.000 description 4
230000003993 interaction Effects 0.000 description 4
239000007788 liquid Substances 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
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 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
240000002791 Brassica napus Species 0.000 description 3
235000004977 Brassica sinapistrum Nutrition 0.000 description 3
240000008067 Cucumis sativus Species 0.000 description 3
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235000007340 Hordeum vulgare Nutrition 0.000 description 3
235000007688 Lycopersicon esculentum Nutrition 0.000 description 3
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
229910052782 aluminium Inorganic materials 0.000 description 3
230000000844 anti-bacterial effect Effects 0.000 description 3
235000021016 apples Nutrition 0.000 description 3
239000007900 aqueous suspension Substances 0.000 description 3
239000003899 bactericide agent Substances 0.000 description 3
JFDZBHWFFUWGJE-UHFFFAOYSA-N benzonitrile Chemical compound N#CC1=CC=CC=C1 JFDZBHWFFUWGJE-UHFFFAOYSA-N 0.000 description 3
PASDCCFISLVPSO-UHFFFAOYSA-N benzoyl chloride Chemical compound ClC(=O)C1=CC=CC=C1 PASDCCFISLVPSO-UHFFFAOYSA-N 0.000 description 3
239000000969 carrier Substances 0.000 description 3
238000007796 conventional method Methods 0.000 description 3
230000006378 damage Effects 0.000 description 3
238000005516 engineering process Methods 0.000 description 3
125000001033 ether group Chemical group 0.000 description 3
235000013305 food Nutrition 0.000 description 3
239000007789 gas Substances 0.000 description 3
239000004009 herbicide Substances 0.000 description 3
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
235000016709 nutrition Nutrition 0.000 description 3
230000008635 plant growth Effects 0.000 description 3
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102000004169 proteins and genes Human genes 0.000 description 3
150000003839 salts Chemical class 0.000 description 3
239000011734 sodium Substances 0.000 description 3
238000001228 spectrum Methods 0.000 description 3
238000005507 spraying Methods 0.000 description 3
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
WNZQDUSMALZDQF-UHFFFAOYSA-N 2-benzofuran-1(3H)-one Chemical compound C1=CC=C2C(=O)OCC2=C1 WNZQDUSMALZDQF-UHFFFAOYSA-N 0.000 description 2
125000006276 2-bromophenyl group Chemical group [H]C1=C([H])C(Br)=C(*)C([H])=C1[H] 0.000 description 2
125000004182 2-chlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(*)C([H])=C1[H] 0.000 description 2
125000006304 2-iodophenyl group Chemical group [H]C1=C([H])C(I)=C(*)C([H])=C1[H] 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
KLCNJIQZXOQYTE-UHFFFAOYSA-N 4,4-dimethylpent-1-ene Chemical compound CC(C)(C)CC=C KLCNJIQZXOQYTE-UHFFFAOYSA-N 0.000 description 2
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
239000005660 Abamectin Substances 0.000 description 2
229920001817 Agar Polymers 0.000 description 2
239000005877 Alpha-Cypermethrin Substances 0.000 description 2
FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 2
CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
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241000195493 Cryptophyta Species 0.000 description 2
MDNWOSOZYLHTCG-UHFFFAOYSA-N Dichlorophen Chemical compound OC1=CC=C(Cl)C=C1CC1=CC(Cl)=CC=C1O MDNWOSOZYLHTCG-UHFFFAOYSA-N 0.000 description 2
XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 2
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DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
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FPIPGXGPPPQFEQ-OVSJKPMPSA-N all-trans-retinol Chemical compound OC\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-OVSJKPMPSA-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
WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
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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
LESVOLZBIFDZGS-UHFFFAOYSA-N vamidothion Chemical compound CNC(=O)C(C)SCCSP(=O)(OC)OC LESVOLZBIFDZGS-UHFFFAOYSA-N 0.000 description 1
239000002966 varnish Substances 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
239000011701 zinc Substances 0.000 description 1
229910052725 zinc Inorganic materials 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

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)

UAA200500915A 2002-07-02 2003-06-20 Phenyl benzamides and agent for controlling undesired microorganisms based thereon UA78340C2 (en)

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
UA78340C2 true UA78340C2 (en)	2007-03-15

Family

ID=29723619

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
UAA200500915A UA78340C2 (en)	2002-07-02	2003-06-20	Phenyl benzamides and agent for controlling undesired microorganisms based thereon

Country Status (18)

Country	Link
US (1)	US7314958B2 (de)
EP (1)	EP1519913A1 (de)
JP (1)	JP4520299B2 (de)
KR (1)	KR101025742B1 (de)
CN (1)	CN1324005C (de)
AR (1)	AR039743A1 (de)
AU (1)	AU2003245975A1 (de)
BR (1)	BR0312407B1 (de)
CA (1)	CA2491368A1 (de)
DE (1)	DE10229595A1 (de)
EA (1)	EA009884B1 (de)
IL (1)	IL165925A (de)
MX (1)	MXPA05000114A (de)
PL (1)	PL374466A1 (de)
TW (1)	TW200413284A (de)
UA (1)	UA78340C2 (de)
WO (1)	WO2004005242A1 (de)
ZA (1)	ZA200500014B (de)

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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
MXPA06006744A (es) *	2003-12-18	2006-08-18	Bayer Cropscience Ag	Carboxamidas opticamente activas y su empleo para la lucha contra microorganismos indeseables.
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
ES2351440T3 (es) *	2005-04-28	2011-02-04	Bayer Cropscience Ag	Combinaciones de principios activos.
DE102005022147A1 (de) *	2005-04-28	2006-11-02	Bayer Cropscience Ag	Wirkstoffkombinationen
EP2255648A3 (de)	2005-06-09	2011-03-02	Bayer CropScience AG	Wirkstoffkombinationen
DE102005026482A1 (de)	2005-06-09	2006-12-14	Bayer Cropscience Ag	Wirkstoffkombinationen
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
CN101646343A (zh) *	2007-02-14	2010-02-10	巴斯夫欧洲公司	诱导植物的病毒耐受性的方法
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
ES2986570T3 (es) *	2008-02-05	2024-11-11	Basf Se	Composición de salud de plantas
EA019439B1 (ru) *	2008-10-21	2014-03-31	Басф Се	Применение карбоксамидов на культивируемых растениях
EP2410850A2 (de)	2009-03-25	2012-02-01	Bayer Cropscience AG	Synergistische wirkstoffkombinationen
AU2010272872B2 (en)	2009-07-16	2014-08-28	Bayer Intellectual Property Gmbh	Synergistic active substance combinations containing phenyl triazoles
WO2011069890A2 (en)	2009-12-08	2011-06-16	Basf Se	Pesticidal mixtures
BR112012013096A2 (pt)	2009-12-08	2015-09-15	Basf Se	mistura agroquímica para aumentar a saúde de uma planta, composição pesticida, método para aperfeiçoamento da saúde de uma planta e uso de uma planta
TWI501727B (zh)	2010-05-28	2015-10-01	Basf Se	農藥混合物
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 (de)	2015-05-05	2015-08-26	Bayer CropScience AG	Wirkstoffkombinationen mit insektiziden eigenschaften
BR112019007468B1 (pt)	2016-10-14	2023-02-14	Pi Industries Ltd	Derivados da fenilamina 4-substituídos e seu uso para proteger as culturas combatendo microrganismos fitopatogênicos indesejáveis
BR112019007483B1 (pt)	2016-10-14	2023-10-17	Pi Industries Ltd	Derivados da fenilamina 4-substituídos e seu uso para proteger as culturas combatendo microrganismos fitopatogênicos indesejáveis
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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

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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
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2002
- 2002-07-02 DE DE10229595A patent/DE10229595A1/de not_active Withdrawn
2003
- 2003-06-20 AU AU2003245975A patent/AU2003245975A1/en not_active Abandoned
- 2003-06-20 BR BRPI0312407-0A patent/BR0312407B1/pt not_active IP Right Cessation
- 2003-06-20 UA UAA200500915A patent/UA78340C2/uk unknown
- 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 WO PCT/EP2003/006512 patent/WO2004005242A1/de not_active Ceased
- 2003-06-20 MX MXPA05000114A patent/MXPA05000114A/es active IP Right Grant
- 2003-06-20 EA EA200500037A patent/EA009884B1/ru not_active IP Right Cessation
- 2003-06-20 US US10/518,446 patent/US7314958B2/en not_active Expired - Fee Related
- 2003-06-20 CN CNB038208121A patent/CN1324005C/zh not_active Expired - Fee Related
- 2003-06-20 CA CA002491368A patent/CA2491368A1/en not_active Abandoned
- 2003-06-20 JP JP2004518548A patent/JP4520299B2/ja not_active Expired - Fee Related
- 2003-06-20 EP EP03738073A patent/EP1519913A1/de not_active Withdrawn
- 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
EA009884B1 (ru)	2008-04-28
AR039743A1 (es)	2005-03-09
PL374466A1 (en)	2005-10-31
CN1678567A (zh)	2005-10-05
TW200413284A (en)	2004-08-01
CA2491368A1 (en)	2004-01-15
WO2004005242A1 (de)	2004-01-15
EP1519913A1 (de)	2005-04-06
BR0312407A (pt)	2005-04-26
US20060211771A1 (en)	2006-09-21
US7314958B2 (en)	2008-01-01
IL165925A (en)	2009-12-24
IL165925A0 (en)	2006-01-15
JP2006503809A (ja)	2006-02-02
AU2003245975A1 (en)	2004-01-23
KR20050016657A (ko)	2005-02-21
KR101025742B1 (ko)	2011-04-04
JP4520299B2 (ja)	2010-08-04
ZA200500014B (en)	2006-06-28
CN1324005C (zh)	2007-07-04
BR0312407B1 (pt)	2014-03-25
EA200500037A1 (ru)	2005-06-30
MXPA05000114A (es)	2005-04-08
DE10229595A1 (de)	2004-01-15

Publication	Publication Date	Title
UA78340C2 (en)	2007-03-15	Phenyl benzamides and agent for controlling undesired microorganisms based thereon
AU2018249817B2 (en)	2024-07-11	Agricultural compositions for improved crop productivity and enhanced phenotypes
UA79266C2 (en)	2007-06-11	Difluoromethyl thiazolyl carboxanilides, and agent and a method for controlling undesired microorganisms
JP5204799B2 (ja)	2013-06-05	殺菌剤としてのピラゾリルカルボキサニリド
UA77546C2 (en)	2006-12-15	Pyrazolepyrimidines and using thereof to control harmful organisms
PL215623B1 (pl)	2014-01-31	Tiazolilokarboksyanilidy, sposób ich wytwarzania, srodek do zwalczania niepozadanych mikroorganizmów, zastosowanie tiazolilokarboksyanilidów, sposób zwalczania niepozadanych mikroorganizmów oraz sposób wytwarzania srodków do zwalczania niepozadanych mikroorganizmów
UA80115C2 (en)	2007-08-27	Disubstituted pyrazolyl carboxanilides, agent based thereon, method for combating undesired microorganisms and intermediates
BRPI0710774A2 (pt)	2011-06-21	método para proteger plantas após germinação contra o ataque de fungos fitopatogênicos foliares, formulação para tratamento de semente, semente, e, uso de pelo menos um composto
JP2009514908A (ja)	2009-04-09	種子を処理するための相乗殺虫混合物
EA016724B1 (ru)	2012-07-30	Средство для защиты растений и его применение
RU2554930C2 (ru)	2015-07-10	Кристаллические модификации протиоконазола
UA79242C2 (en)	2007-06-11	Spirocyclic 3-phenyl-3-substituted 4-ketolactams and 4-ketolactones, process for preparation thereof (variants)
JP4922927B2 (ja)	2012-04-25	相乗的殺虫剤混合物
ES2314234T3 (es)	2009-03-16	Furanocarboxamidas.
JP4757490B2 (ja)	2011-08-24	２−［２−（１−クロロシクロプロピル）−３−（２−クロロフェニル）−２−ヒドロキシプロピル］−２，４−ジヒドロ−３ｈ−１，２，４−トリアゾール−３−チオンの結晶変態ｉｉ型
UA81924C2 (uk)	2008-02-25	Тіазолілбіфеніламіди, засіб та їх застосування для боротьби із небажаними мікроорганізмами
UA82083C2 (en)	2008-03-11	3-phenyl substituted 3-substituted-4-ketolactams and ketolactones
ES2294687T3 (es)	2008-04-01	Combinaciones de principios activos fungicidas.
JP2005528364A (ja)	2005-09-22	トリアゾロピリミジン類
CN1984563A (zh)	2007-06-20	取代的1h－吡咯－2,5－二酮
KR20030059332A (ko)	2003-07-07	디클로로피리딜 메틸 시안아미딘
MXPA06011995A (es)	2007-04-20	Mezclas sinergicas insecticidas