JP2004262940A5 - - Google Patents
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- Publication number
- JP2004262940A5 JP2004262940A5 JP2004036026A JP2004036026A JP2004262940A5 JP 2004262940 A5 JP2004262940 A5 JP 2004262940A5 JP 2004036026 A JP2004036026 A JP 2004036026A JP 2004036026 A JP2004036026 A JP 2004036026A JP 2004262940 A5 JP2004262940 A5 JP 2004262940A5
- Authority
- JP
- Japan
- Prior art keywords
- group
- atom
- substituent
- alkyl
- bromine
- 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.)
- Granted
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- 125000001424 substituent group Chemical group 0.000 claims 110
- 229910052801 chlorine Inorganic materials 0.000 claims 60
- 125000001309 chloro group Chemical group Cl* 0.000 claims 57
- 125000001153 fluoro group Chemical group F* 0.000 claims 56
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 51
- 229910052731 fluorine Inorganic materials 0.000 claims 50
- 125000005843 halogen group Chemical group 0.000 claims 36
- 125000004093 cyano group Chemical group *C#N 0.000 claims 28
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 claims 26
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 26
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims 18
- 230000002363 herbicidal effect Effects 0.000 claims 18
- 125000006583 (C1-C3) haloalkyl group Chemical group 0.000 claims 14
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 14
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 13
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims 13
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims 12
- 229910052740 iodine Inorganic materials 0.000 claims 12
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims 10
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 9
- 229910052794 bromium Inorganic materials 0.000 claims 9
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 9
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims 8
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims 8
- 229910052757 nitrogen Inorganic materials 0.000 claims 8
- 125000004430 oxygen atom Chemical group O* 0.000 claims 8
- 229910052717 sulfur Inorganic materials 0.000 claims 8
- 125000004434 sulfur atom Chemical group 0.000 claims 8
- 150000001875 compounds Chemical class 0.000 claims 7
- 125000000623 heterocyclic group Chemical group 0.000 claims 7
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 7
- -1 phenylsulfonyloxy group Chemical group 0.000 claims 7
- 125000004429 atom Chemical group 0.000 claims 6
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims 5
- 125000006828 (C2-C7) alkoxycarbonyl group Chemical group 0.000 claims 5
- 125000006773 (C2-C7) alkylcarbonyl group Chemical group 0.000 claims 5
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 5
- 125000000217 alkyl group Chemical group 0.000 claims 5
- 239000000460 chlorine Substances 0.000 claims 5
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 5
- 125000004455 (C1-C3) alkylthio group Chemical group 0.000 claims 4
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 4
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims 4
- 125000004070 6 membered heterocyclic group Chemical group 0.000 claims 4
- 125000003545 alkoxy group Chemical group 0.000 claims 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 4
- 125000003356 phenylsulfanyl group Chemical group [*]SC1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims 4
- 125000004738 (C1-C6) alkyl sulfinyl group Chemical group 0.000 claims 3
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 claims 3
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 claims 3
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims 3
- 125000006645 (C3-C4) cycloalkyl group Chemical group 0.000 claims 3
- 125000006569 (C5-C6) heterocyclic group Chemical group 0.000 claims 3
- 125000002373 5 membered heterocyclic group Chemical group 0.000 claims 3
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims 3
- 229910052799 carbon Inorganic materials 0.000 claims 3
- 229910052736 halogen Inorganic materials 0.000 claims 3
- 150000002367 halogens Chemical class 0.000 claims 3
- 125000001820 oxy group Chemical group [*:1]O[*:2] 0.000 claims 3
- 125000006677 (C1-C3) haloalkoxy group Chemical group 0.000 claims 2
- 125000004844 (C1-C6) alkoxyimino group Chemical group 0.000 claims 2
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 claims 2
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims 2
- 125000003277 amino group Chemical group 0.000 claims 2
- 150000001602 bicycloalkyls Chemical group 0.000 claims 2
- 150000001721 carbon Chemical group 0.000 claims 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 2
- 125000003754 ethoxycarbonyl group Chemical group C(=O)(OCC)* 0.000 claims 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 2
- 125000002541 furyl group Chemical group 0.000 claims 2
- 125000001188 haloalkyl group Chemical group 0.000 claims 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 2
- ZTHRQJQJODGZHV-UHFFFAOYSA-N n-phenylpropanamide Chemical compound CCC(=O)NC1=CC=CC=C1 ZTHRQJQJODGZHV-UHFFFAOYSA-N 0.000 claims 2
- 125000003808 silyl group Chemical group [H][Si]([H])([H])[*] 0.000 claims 2
- 125000001544 thienyl group Chemical group 0.000 claims 2
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 claims 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 2
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 claims 2
- AAILEWXSEQLMNI-UHFFFAOYSA-N 1h-pyridazin-6-one Chemical compound OC1=CC=CN=N1 AAILEWXSEQLMNI-UHFFFAOYSA-N 0.000 claims 1
- CJSZUDRFDBPZFG-UHFFFAOYSA-N 3-(1-benzofuran-7-yloxy)-6-chloro-1h-pyridazin-4-one Chemical compound OC1=CC(Cl)=NN=C1OC1=CC=CC2=C1OC=C2 CJSZUDRFDBPZFG-UHFFFAOYSA-N 0.000 claims 1
- YLBGKIGQWGWJAV-UHFFFAOYSA-N 3-(2-bromo-6-methylphenoxy)-6-chloro-1h-pyridazin-4-one Chemical compound CC1=CC=CC(Br)=C1OC1=NN=C(Cl)C=C1O YLBGKIGQWGWJAV-UHFFFAOYSA-N 0.000 claims 1
- IWKQMRRGGSDCBA-UHFFFAOYSA-N 3-phenoxy-1h-pyridazin-4-one Chemical class OC1=CC=NN=C1OC1=CC=CC=C1 IWKQMRRGGSDCBA-UHFFFAOYSA-N 0.000 claims 1
- LCUOPTJBJVESIM-UHFFFAOYSA-N 6-chloro-3-(2,3,5,6-tetramethylphenoxy)-1h-pyridazin-4-one Chemical compound CC1=CC(C)=C(C)C(OC=2C(=CC(Cl)=NN=2)O)=C1C LCUOPTJBJVESIM-UHFFFAOYSA-N 0.000 claims 1
- NREOCHFMYBRODV-UHFFFAOYSA-N 6-chloro-3-(2,3-dihydro-1h-inden-4-yloxy)-1h-pyridazin-4-one Chemical compound OC1=CC(Cl)=NN=C1OC1=CC=CC2=C1CCC2 NREOCHFMYBRODV-UHFFFAOYSA-N 0.000 claims 1
- WPYJITAQNCYWTA-UHFFFAOYSA-N 6-chloro-3-(2,5-dimethylphenoxy)-1h-pyridazin-4-one Chemical compound CC1=CC=C(C)C(OC=2C(=CC(Cl)=NN=2)O)=C1 WPYJITAQNCYWTA-UHFFFAOYSA-N 0.000 claims 1
- MDOUHXIYRZVOBZ-UHFFFAOYSA-N 6-chloro-3-(2-chloro-6-cyclopropylphenoxy)-1h-pyridazin-4-one Chemical compound OC1=CC(Cl)=NN=C1OC1=C(Cl)C=CC=C1C1CC1 MDOUHXIYRZVOBZ-UHFFFAOYSA-N 0.000 claims 1
- XRVGAOMMMOFTEL-UHFFFAOYSA-N 6-chloro-3-(2-chloro-6-methylphenoxy)-1h-pyridazin-4-one Chemical compound CC1=CC=CC(Cl)=C1OC1=NN=C(Cl)C=C1O XRVGAOMMMOFTEL-UHFFFAOYSA-N 0.000 claims 1
- AARKZRZYPICLJC-UHFFFAOYSA-N 6-chloro-3-(2-cyclopropyl-3,5-dimethylphenoxy)-1h-pyridazin-4-one Chemical compound N=1N=C(Cl)C=C(O)C=1OC1=CC(C)=CC(C)=C1C1CC1 AARKZRZYPICLJC-UHFFFAOYSA-N 0.000 claims 1
- GZJVZGUUTYWVTP-UHFFFAOYSA-N 6-chloro-3-(2-cyclopropyl-6-methylphenoxy)-1h-pyridazin-4-one Chemical compound N=1N=C(Cl)C=C(O)C=1OC=1C(C)=CC=CC=1C1CC1 GZJVZGUUTYWVTP-UHFFFAOYSA-N 0.000 claims 1
- AIRLWQYEZCTFPD-UHFFFAOYSA-N 6-chloro-3-(2-cyclopropylphenoxy)-1h-pyridazin-4-one Chemical compound OC1=CC(Cl)=NN=C1OC1=CC=CC=C1C1CC1 AIRLWQYEZCTFPD-UHFFFAOYSA-N 0.000 claims 1
- VXILURWSAZHSSO-UHFFFAOYSA-N 6-chloro-3-(2-iodophenoxy)-1h-pyridazin-4-one Chemical compound OC1=CC(Cl)=NN=C1OC1=CC=CC=C1I VXILURWSAZHSSO-UHFFFAOYSA-N 0.000 claims 1
- QZIJCVNSXFTMKH-UHFFFAOYSA-N 6-chloro-3-(2-methoxy-5-methylphenoxy)-1h-pyridazin-4-one Chemical compound COC1=CC=C(C)C=C1OC1=NN=C(Cl)C=C1O QZIJCVNSXFTMKH-UHFFFAOYSA-N 0.000 claims 1
- QFFRMJJGHVACFL-UHFFFAOYSA-N 6-chloro-3-(2-methylphenoxy)-1h-pyridazin-4-one Chemical compound CC1=CC=CC=C1OC1=NN=C(Cl)C=C1O QFFRMJJGHVACFL-UHFFFAOYSA-N 0.000 claims 1
- WHVOTWUPXVPFKJ-UHFFFAOYSA-N 6-chloro-3-(2-propan-2-ylphenoxy)-1h-pyridazin-4-one Chemical compound CC(C)C1=CC=CC=C1OC1=NN=C(Cl)C=C1O WHVOTWUPXVPFKJ-UHFFFAOYSA-N 0.000 claims 1
- QGQSRQPXXMTJCM-UHFFFAOYSA-N Benfuresate Chemical compound CCS(=O)(=O)OC1=CC=C2OCC(C)(C)C2=C1 QGQSRQPXXMTJCM-UHFFFAOYSA-N 0.000 claims 1
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
- UWVKRNOCDUPIDM-UHFFFAOYSA-N Ethoxysulfuron Chemical compound CCOC1=CC=CC=C1OS(=O)(=O)NC(=O)NC1=NC(OC)=CC(OC)=N1 UWVKRNOCDUPIDM-UHFFFAOYSA-N 0.000 claims 1
- LLQPHQFNMLZJMP-UHFFFAOYSA-N Fentrazamide Chemical compound N1=NN(C=2C(=CC=CC=2)Cl)C(=O)N1C(=O)N(CC)C1CCCCC1 LLQPHQFNMLZJMP-UHFFFAOYSA-N 0.000 claims 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
- FCOHEOSCARXMMS-UHFFFAOYSA-N Oxaziclomefone Chemical compound C1OC(C)=C(C=2C=CC=CC=2)C(=O)N1C(C)(C)C1=CC(Cl)=CC(Cl)=C1 FCOHEOSCARXMMS-UHFFFAOYSA-N 0.000 claims 1
- 239000004480 active ingredient Substances 0.000 claims 1
- 125000000676 alkoxyimino group Chemical group 0.000 claims 1
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 claims 1
- 125000001246 bromo group Chemical group Br* 0.000 claims 1
- 125000004122 cyclic group Chemical group 0.000 claims 1
- 125000000753 cycloalkyl group Chemical group 0.000 claims 1
- 150000002148 esters Chemical class 0.000 claims 1
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 claims 1
- 125000005842 heteroatom Chemical group 0.000 claims 1
- 239000001257 hydrogen Substances 0.000 claims 1
- 229910052739 hydrogen Inorganic materials 0.000 claims 1
- 125000004043 oxo group Chemical group O=* 0.000 claims 1
- 125000003170 phenylsulfonyl group Chemical group C1(=CC=CC=C1)S(=O)(=O)* 0.000 claims 1
- 150000003839 salts Chemical class 0.000 claims 1
- SNOOUWRIMMFWNE-UHFFFAOYSA-M sodium;6-[(3,4,5-trimethoxybenzoyl)amino]hexanoate Chemical group [Na+].COC1=CC(C(=O)NCCCCCC([O-])=O)=CC(OC)=C1OC SNOOUWRIMMFWNE-UHFFFAOYSA-M 0.000 claims 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims 1
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2004036026A JP4580176B2 (ja) | 2003-02-13 | 2004-02-13 | ３−フェノキシ−４−ピリダジノール誘導体を含有する除草組成物 |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2003035018 | 2003-02-13 | ||
| JP2004036026A JP4580176B2 (ja) | 2003-02-13 | 2004-02-13 | ３−フェノキシ−４−ピリダジノール誘導体を含有する除草組成物 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2004262940A JP2004262940A (ja) | 2004-09-24 |
| JP2004262940A5 true JP2004262940A5 (enrdf_load_stackoverflow) | 2007-04-05 |
| JP4580176B2 JP4580176B2 (ja) | 2010-11-10 |
Family
ID=33133929
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2004036026A Expired - Lifetime JP4580176B2 (ja) | 2003-02-13 | 2004-02-13 | ３−フェノキシ−４−ピリダジノール誘導体を含有する除草組成物 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP4580176B2 (enrdf_load_stackoverflow) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4549690B2 (ja) * | 2003-02-13 | 2010-09-22 | 三井化学アグロ株式会社 | ３−フェノキシ−４−ピリダジノール誘導体を含有する除草性組成物 |
| JP5106839B2 (ja) * | 2006-11-30 | 2012-12-26 | 三井化学アグロ株式会社 | 除草性組成物 |
| JP5399041B2 (ja) * | 2008-10-31 | 2014-01-29 | 三井化学アグロ株式会社 | 除草性組成物 |
| JP5546912B2 (ja) * | 2010-03-12 | 2014-07-09 | 三井化学アグロ株式会社 | 除草性組成物 |
| JP5898543B2 (ja) | 2012-03-23 | 2016-04-06 | 三井化学アグロ株式会社 | 除草性組成物 |
| CN107018981A (zh) * | 2017-05-27 | 2017-08-08 | 北京科发伟业农药技术中心 | 一种含噁嗪草酮的除草组合物 |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4128048B2 (ja) * | 2001-08-17 | 2008-07-30 | 三共アグロ株式会社 | ３−フェノキシ−４−ピリダジノール誘導体及びそれを含有する除草剤組成物 |
-
2004
- 2004-02-13 JP JP2004036026A patent/JP4580176B2/ja not_active Expired - Lifetime