JP2014533254A - 置換型１，２，５−オキサジアゾール化合物及びその除草剤としての使用 - Google Patents
置換型１，２，５−オキサジアゾール化合物及びその除草剤としての使用 Download PDFInfo
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- JP2014533254A JP2014533254A JP2014540513A JP2014540513A JP2014533254A JP 2014533254 A JP2014533254 A JP 2014533254A JP 2014540513 A JP2014540513 A JP 2014540513A JP 2014540513 A JP2014540513 A JP 2014540513A JP 2014533254 A JP2014533254 A JP 2014533254A
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- JP
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- Prior art keywords
- alkyl
- isoxazolinyl
- group
- alkoxy
- haloalkyl
- 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.)
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- 150000002244 furazanes Chemical class 0.000 title claims abstract description 6
- 239000004009 herbicide Substances 0.000 title description 20
- -1 1,2,5-oxadiazole compound Chemical class 0.000 claims abstract description 701
- 150000001875 compounds Chemical class 0.000 claims abstract description 230
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 108
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 107
- 150000002367 halogens Chemical class 0.000 claims abstract description 104
- 239000001257 hydrogen Substances 0.000 claims abstract description 91
- 239000000203 mixture Substances 0.000 claims abstract description 85
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims abstract description 75
- 150000002431 hydrogen Chemical class 0.000 claims abstract description 69
- 150000003839 salts Chemical class 0.000 claims abstract description 55
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims abstract description 46
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims abstract description 45
- 125000006643 (C2-C6) haloalkenyl group Chemical group 0.000 claims abstract description 37
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims abstract description 37
- 150000001204 N-oxides Chemical class 0.000 claims abstract description 21
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims abstract description 21
- 125000004093 cyano group Chemical group *C#N 0.000 claims abstract description 14
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 claims abstract description 7
- 125000004649 C2-C8 alkynyl group Chemical group 0.000 claims abstract description 7
- 125000006766 (C2-C6) alkynyloxy group Chemical group 0.000 claims abstract description 5
- 125000003320 C2-C6 alkenyloxy group Chemical group 0.000 claims abstract description 5
- 125000004648 C2-C8 alkenyl group Chemical group 0.000 claims abstract description 5
- 125000001181 organosilyl group Chemical group [SiH3]* 0.000 claims abstract description 3
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 238
- 125000000623 heterocyclic group Chemical group 0.000 claims description 89
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 79
- 239000000460 chlorine Substances 0.000 claims description 71
- SNOOUWRIMMFWNE-UHFFFAOYSA-M sodium;6-[(3,4,5-trimethoxybenzoyl)amino]hexanoate Chemical compound [Na+].COC1=CC(C(=O)NCCCCCC([O-])=O)=CC(OC)=C1OC SNOOUWRIMMFWNE-UHFFFAOYSA-M 0.000 claims description 66
- 229910052757 nitrogen Inorganic materials 0.000 claims description 58
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 41
- 229910052801 chlorine Inorganic materials 0.000 claims description 41
- 229910052760 oxygen Inorganic materials 0.000 claims description 41
- 229910052731 fluorine Inorganic materials 0.000 claims description 40
- 229920006395 saturated elastomer Polymers 0.000 claims description 40
- 229910052717 sulfur Inorganic materials 0.000 claims description 40
- 125000005842 heteroatom Chemical group 0.000 claims description 38
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 claims description 33
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 26
- 125000002950 monocyclic group Chemical group 0.000 claims description 25
- 125000000217 alkyl group Chemical group 0.000 claims description 23
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 23
- YUCFVHQCAFKDQG-UHFFFAOYSA-N fluoromethane Chemical compound F[CH] YUCFVHQCAFKDQG-UHFFFAOYSA-N 0.000 claims description 22
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 21
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 17
- 229910052799 carbon Inorganic materials 0.000 claims description 16
- 125000003545 alkoxy group Chemical group 0.000 claims description 15
- 125000002619 bicyclic group Chemical group 0.000 claims description 15
- 239000011737 fluorine Substances 0.000 claims description 15
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 14
- 125000001188 haloalkyl group Chemical group 0.000 claims description 14
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 14
- 125000006656 (C2-C4) alkenyl group Chemical group 0.000 claims description 13
- 125000004438 haloalkoxy group Chemical group 0.000 claims description 13
- 125000006615 aromatic heterocyclic group Chemical group 0.000 claims description 12
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 12
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 12
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 12
- 125000006650 (C2-C4) alkynyl group Chemical group 0.000 claims description 10
- 239000002671 adjuvant Substances 0.000 claims description 10
- 239000003905 agrochemical Substances 0.000 claims description 10
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 9
- 125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 claims description 9
- 238000006467 substitution reaction Methods 0.000 claims description 7
- 125000004122 cyclic group Chemical group 0.000 claims description 6
- 125000000842 isoxazolyl group Chemical group 0.000 claims description 6
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims description 5
- 125000004429 atom Chemical group 0.000 claims description 4
- 125000005844 heterocyclyloxy group Chemical group 0.000 claims description 4
- 125000003971 isoxazolinyl group Chemical group 0.000 claims description 4
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims description 3
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 3
- 125000004076 pyridyl group Chemical group 0.000 claims description 3
- 125000000714 pyrimidinyl group Chemical group 0.000 claims description 3
- 125000005879 dioxolanyl group Chemical group 0.000 claims description 2
- 125000002541 furyl group Chemical group 0.000 claims description 2
- 125000002757 morpholinyl group Chemical group 0.000 claims description 2
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 2
- 125000002971 oxazolyl group Chemical group 0.000 claims description 2
- 125000004193 piperazinyl group Chemical group 0.000 claims description 2
- 125000003386 piperidinyl group Chemical group 0.000 claims description 2
- 125000003373 pyrazinyl group Chemical group 0.000 claims description 2
- 125000003226 pyrazolyl group Chemical group 0.000 claims description 2
- 125000003718 tetrahydrofuranyl group Chemical group 0.000 claims description 2
- 125000000335 thiazolyl group Chemical group 0.000 claims description 2
- 125000005133 alkynyloxy group Chemical group 0.000 claims 1
- 238000000034 method Methods 0.000 abstract description 31
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract description 4
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract description 4
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- 125000004209 (C1-C8) alkyl group Chemical group 0.000 abstract 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 abstract 1
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- 238000009472 formulation Methods 0.000 description 17
- 239000003112 inhibitor Substances 0.000 description 17
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- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-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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- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 14
- 239000000049 pigment Substances 0.000 description 14
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- 238000006243 chemical reaction Methods 0.000 description 12
- 150000003254 radicals Chemical class 0.000 description 12
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 description 11
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- LMDZBCPBFSXMTL-UHFFFAOYSA-N 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide Chemical compound CCN=C=NCCCN(C)C LMDZBCPBFSXMTL-UHFFFAOYSA-N 0.000 description 6
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- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 description 6
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- YNESATAKKCNGOF-UHFFFAOYSA-N lithium bis(trimethylsilyl)amide Chemical compound [Li+].C[Si](C)(C)[N-][Si](C)(C)C YNESATAKKCNGOF-UHFFFAOYSA-N 0.000 description 6
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- 125000004853 tetrahydropyridinyl group Chemical group N1(CCCC=C1)* 0.000 description 1
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 1
- QEMXHQIAXOOASZ-UHFFFAOYSA-N tetramethylammonium Chemical compound C[N+](C)(C)C QEMXHQIAXOOASZ-UHFFFAOYSA-N 0.000 description 1
- WROMPOXWARCANT-UHFFFAOYSA-N tfa trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F.OC(=O)C(F)(F)F WROMPOXWARCANT-UHFFFAOYSA-N 0.000 description 1
- 125000004495 thiazol-4-yl group Chemical group S1C=NC(=C1)* 0.000 description 1
- 125000004496 thiazol-5-yl group Chemical group S1C=NC=C1* 0.000 description 1
- 125000004300 thiazolidin-2-yl group Chemical group [H]N1C([H])([H])C([H])([H])SC1([H])* 0.000 description 1
- GLDAZAQRGCSFNP-UHFFFAOYSA-N thiencarbazone Chemical compound O=C1N(C)C(OC)=NN1C(=O)NS(=O)(=O)C1=C(C)SC=C1C(O)=O GLDAZAQRGCSFNP-UHFFFAOYSA-N 0.000 description 1
- XSKZXGDFSCCXQX-UHFFFAOYSA-N thiencarbazone-methyl Chemical compound COC(=O)C1=CSC(C)=C1S(=O)(=O)NC(=O)N1C(=O)N(C)C(OC)=N1 XSKZXGDFSCCXQX-UHFFFAOYSA-N 0.000 description 1
- 125000004275 thietan-2-yl group Chemical group [H]C1([H])SC([H])(*)C1([H])[H] 0.000 description 1
- 125000006300 thietan-3-yl group Chemical group [H]C1([H])SC([H])([H])C1([H])* 0.000 description 1
- LOQQVLXUKHKNIA-UHFFFAOYSA-N thifensulfuron Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C2=C(SC=C2)C(O)=O)=N1 LOQQVLXUKHKNIA-UHFFFAOYSA-N 0.000 description 1
- 150000007970 thio esters Chemical class 0.000 description 1
- 125000004569 thiomorpholin-2-yl group Chemical group N1CC(SCC1)* 0.000 description 1
- 125000004570 thiomorpholin-3-yl group Chemical group N1C(CSCC1)* 0.000 description 1
- 125000004571 thiomorpholin-4-yl group Chemical group N1(CCSCC1)* 0.000 description 1
- 210000001519 tissue Anatomy 0.000 description 1
- 235000010215 titanium dioxide Nutrition 0.000 description 1
- IYMLUHWAJFXAQP-UHFFFAOYSA-N topramezone Chemical compound CC1=C(C(=O)C2=C(N(C)N=C2)O)C=CC(S(C)(=O)=O)=C1C1=NOCC1 IYMLUHWAJFXAQP-UHFFFAOYSA-N 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- 150000003624 transition metals Chemical class 0.000 description 1
- 238000013519 translation Methods 0.000 description 1
- XOPFESVZMSQIKC-UHFFFAOYSA-N triasulfuron Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)OCCCl)=N1 XOPFESVZMSQIKC-UHFFFAOYSA-N 0.000 description 1
- BQZXUHDXIARLEO-UHFFFAOYSA-N tribenuron Chemical compound COC1=NC(C)=NC(N(C)C(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(O)=O)=N1 BQZXUHDXIARLEO-UHFFFAOYSA-N 0.000 description 1
- YMXOXAPKZDWXLY-QWRGUYRKSA-N tribenuron methyl Chemical group COC(=O)[C@H]1CCCC[C@@H]1S(=O)(=O)NC(=O)N(C)C1=NC(C)=NC(OC)=N1 YMXOXAPKZDWXLY-QWRGUYRKSA-N 0.000 description 1
- REEQLXCGVXDJSQ-UHFFFAOYSA-N trichlopyr Chemical compound OC(=O)COC1=NC(Cl)=C(Cl)C=C1Cl REEQLXCGVXDJSQ-UHFFFAOYSA-N 0.000 description 1
- AZHZOGYUMMIAOF-UHFFFAOYSA-N trifludimoxazin Chemical compound O=C1N(C)C(=S)N(C)C(=O)N1C(C(=C1)F)=CC2=C1OC(F)(F)C(=O)N2CC#C AZHZOGYUMMIAOF-UHFFFAOYSA-N 0.000 description 1
- KVEQCVKVIFQSGC-UHFFFAOYSA-N tritosulfuron Chemical compound FC(F)(F)C1=NC(OC)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(F)(F)F)=N1 KVEQCVKVIFQSGC-UHFFFAOYSA-N 0.000 description 1
- 239000002753 trypsin inhibitor Substances 0.000 description 1
- JABYJIQOLGWMQW-UHFFFAOYSA-N undec-4-ene Chemical compound CCCCCCC=CCCC JABYJIQOLGWMQW-UHFFFAOYSA-N 0.000 description 1
- 229940035893 uracil Drugs 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 150000004669 very long chain fatty acids Chemical class 0.000 description 1
- 230000003612 virological effect Effects 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 239000003021 water soluble solvent Substances 0.000 description 1
- 239000004563 wettable powder Substances 0.000 description 1
- 230000002087 whitening effect Effects 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000000230 xanthan gum Substances 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- 235000010493 xanthan gum Nutrition 0.000 description 1
- 229940082509 xanthan gum Drugs 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 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
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/82—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with three ring hetero atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D271/00—Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms
- C07D271/02—Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms not condensed with other rings
- C07D271/08—1,2,5-Oxadiazoles; Hydrogenated 1,2,5-oxadiazoles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Plural Heterocyclic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201161559164P | 2011-11-14 | 2011-11-14 | |
| US61/559,164 | 2011-11-14 | ||
| PCT/EP2012/072469 WO2013072300A1 (en) | 2011-11-14 | 2012-11-13 | Substituted 1,2,5-oxadiazole compounds and their use as herbicides |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JP2014533254A true JP2014533254A (ja) | 2014-12-11 |
Family
ID=47146426
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2014540513A Pending JP2014533254A (ja) | 2011-11-14 | 2012-11-13 | 置換型１，２，５−オキサジアゾール化合物及びその除草剤としての使用 |
Country Status (17)
| Country | Link |
|---|---|
| US (1) | US20140323306A1 (enExample) |
| EP (1) | EP2780334A1 (enExample) |
| JP (1) | JP2014533254A (enExample) |
| KR (1) | KR20140098134A (enExample) |
| CN (1) | CN104039770A (enExample) |
| AR (1) | AR088857A1 (enExample) |
| AU (1) | AU2012338953A1 (enExample) |
| BR (1) | BR112014011534A2 (enExample) |
| CA (1) | CA2853724A1 (enExample) |
| CO (1) | CO6950497A2 (enExample) |
| CR (1) | CR20140195A (enExample) |
| EA (1) | EA201400576A1 (enExample) |
| IL (1) | IL232235A0 (enExample) |
| IN (1) | IN2014CN03268A (enExample) |
| MX (1) | MX2014005175A (enExample) |
| WO (1) | WO2013072300A1 (enExample) |
| ZA (1) | ZA201404294B (enExample) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2019500365A (ja) * | 2015-12-17 | 2019-01-10 | ビーエーエスエフ ソシエタス・ヨーロピアＢａｓｆ Ｓｅ | ベンズアミド化合物及び除草剤としてのそれらの使用 |
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| CN104053656A (zh) | 2011-11-16 | 2014-09-17 | 巴斯夫欧洲公司 | 取代的1,2,5-噁二唑化合物及其作为除草剂的用途ii |
| WO2014184058A1 (en) * | 2013-05-15 | 2014-11-20 | Basf Se | Substituted 1,2,5-oxadiazole compounds and their use as herbicides |
| US9708314B2 (en) | 2013-05-31 | 2017-07-18 | Nissan Chemical Industries, Ltd. | Heterocyclic amide compound |
| US20160280696A1 (en) * | 2013-10-10 | 2016-09-29 | Basf Se | Substituted 1,2,5-oxadiazole compounds and their use as herbicides |
| WO2015052178A1 (en) * | 2013-10-10 | 2015-04-16 | Basf Se | 1,2,5-oxadiazole compounds and their use as herbicides |
| EP2907807A1 (en) | 2014-02-18 | 2015-08-19 | Basf Se | Benzamide compounds and their use as herbicides |
| EP3117003B1 (en) | 2014-03-11 | 2019-10-30 | BASF Agricultural Solutions Seed US LLC | Hppd variants and methods of use |
| US11248234B2 (en) | 2015-02-11 | 2022-02-15 | Basf Se | Herbicide-resistant hydroxyphenylpyruvate dioxygenases |
| US10597674B2 (en) | 2015-09-11 | 2020-03-24 | Basf Agricultural Solutions Seed, Us Llc | HPPD variants and methods of use |
| US11624076B2 (en) | 2016-04-21 | 2023-04-11 | BASF Agricultural Solutions Seed US LLC | TAL-effector mediated herbicide tolerance |
| BR112019018175A2 (pt) | 2017-03-07 | 2020-04-07 | BASF Agricultural Solutions Seed US LLC | molécula, célula, planta, sementes, polipeptídeos recombinantes, método para produzir um polipeptídeo, planta, método para controlar ervas, uso do ácido nucleico e produto de utilidade |
| AR112342A1 (es) | 2017-07-21 | 2019-10-16 | Basf Se | Compuestos de benzamida y su uso como herbicidas |
| BR112020008092A2 (pt) | 2017-10-24 | 2020-09-15 | BASF Agricultural Solutions Seed US LLC | método para conferir tolerância a um herbicida e planta de soja transgênica |
| BR112020008096A2 (pt) | 2017-10-24 | 2020-11-03 | Basf Se | método para conferir tolerância a um herbicida e planta de soja transgênica |
| CA3179394A1 (en) | 2020-04-07 | 2021-10-14 | Bayer Aktiengesellschaft | Substituted isophthalic acid diamides |
| BR112022019768A2 (pt) * | 2020-04-07 | 2022-12-06 | Bayer Ag | Diamidas de ácido isoftálico substituídas |
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-
2012
- 2012-11-13 MX MX2014005175A patent/MX2014005175A/es unknown
- 2012-11-13 EA EA201400576A patent/EA201400576A1/ru unknown
- 2012-11-13 CA CA2853724A patent/CA2853724A1/en not_active Abandoned
- 2012-11-13 WO PCT/EP2012/072469 patent/WO2013072300A1/en not_active Ceased
- 2012-11-13 CN CN201280067032.2A patent/CN104039770A/zh active Pending
- 2012-11-13 BR BR112014011534A patent/BR112014011534A2/pt not_active IP Right Cessation
- 2012-11-13 AU AU2012338953A patent/AU2012338953A1/en not_active Abandoned
- 2012-11-13 EP EP12783624.5A patent/EP2780334A1/en not_active Withdrawn
- 2012-11-13 US US14/357,897 patent/US20140323306A1/en not_active Abandoned
- 2012-11-13 AR ARP120104276A patent/AR088857A1/es unknown
- 2012-11-13 KR KR1020147016251A patent/KR20140098134A/ko not_active Withdrawn
- 2012-11-13 IN IN3268CHN2014 patent/IN2014CN03268A/en unknown
- 2012-11-13 JP JP2014540513A patent/JP2014533254A/ja active Pending
-
2014
- 2014-04-24 IL IL232235A patent/IL232235A0/en unknown
- 2014-04-29 CR CR20140195A patent/CR20140195A/es unknown
- 2014-05-08 CO CO14099141A patent/CO6950497A2/es unknown
- 2014-06-11 ZA ZA2014/04294A patent/ZA201404294B/en unknown
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2019500365A (ja) * | 2015-12-17 | 2019-01-10 | ビーエーエスエフ ソシエタス・ヨーロピアＢａｓｆ Ｓｅ | ベンズアミド化合物及び除草剤としてのそれらの使用 |
Also Published As
| Publication number | Publication date |
|---|---|
| CO6950497A2 (es) | 2014-05-20 |
| MX2014005175A (es) | 2014-05-28 |
| AR088857A1 (es) | 2014-07-10 |
| AU2012338953A1 (en) | 2014-06-05 |
| CN104039770A (zh) | 2014-09-10 |
| CA2853724A1 (en) | 2013-05-23 |
| BR112014011534A2 (pt) | 2017-05-09 |
| KR20140098134A (ko) | 2014-08-07 |
| US20140323306A1 (en) | 2014-10-30 |
| EA201400576A1 (ru) | 2014-11-28 |
| CR20140195A (es) | 2014-06-03 |
| WO2013072300A1 (en) | 2013-05-23 |
| IN2014CN03268A (enExample) | 2015-07-03 |
| ZA201404294B (en) | 2017-11-29 |
| EP2780334A1 (en) | 2014-09-24 |
| IL232235A0 (en) | 2014-06-30 |
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