JP2004262935A5 - - Google Patents
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- Publication number
- JP2004262935A5 JP2004262935A5 JP2004035796A JP2004035796A JP2004262935A5 JP 2004262935 A5 JP2004262935 A5 JP 2004262935A5 JP 2004035796 A JP2004035796 A JP 2004035796A JP 2004035796 A JP2004035796 A JP 2004035796A JP 2004262935 A5 JP2004262935 A5 JP 2004262935A5
- 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 111
- 229910052801 chlorine Inorganic materials 0.000 claims 60
- 125000001309 chloro group Chemical group Cl* 0.000 claims 58
- 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
- -1 phenylsulfonyloxy group Chemical group 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
- 150000001875 compounds Chemical class 0.000 claims 9
- 229910052757 nitrogen 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
- 125000004430 oxygen atom Chemical group O* 0.000 claims 8
- 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 8
- 229910052717 sulfur Inorganic materials 0.000 claims 8
- 125000004434 sulfur atom Chemical group 0.000 claims 8
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 7
- 229910052794 bromium Inorganic materials 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
- 125000002496 methyl group Chemical group [H]C([H])([H])* 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
- 125000003545 alkoxy group Chemical group 0.000 claims 5
- 125000000217 alkyl group Chemical group 0.000 claims 5
- 125000004429 atom Chemical group 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
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 4
- 239000000460 chlorine Substances 0.000 claims 4
- 125000001820 oxy group Chemical group [*:1]O[*:2] 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
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 3
- 229910052736 halogen Inorganic materials 0.000 claims 3
- 150000002367 halogens Chemical class 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
- 125000002541 furyl group Chemical group 0.000 claims 2
- 125000001188 haloalkyl group Chemical group 0.000 claims 2
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 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
- 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
- OVSKIKFHRZPJSS-DOMIDYPGSA-N 2-(2,4-dichlorophenoxy)acetic acid Chemical compound OC(=O)[14CH2]OC1=CC=C(Cl)C=C1Cl OVSKIKFHRZPJSS-DOMIDYPGSA-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
- DVOODWOZJVJKQR-UHFFFAOYSA-N 5-tert-butyl-3-(2,4-dichloro-5-prop-2-ynoxyphenyl)-1,3,4-oxadiazol-2-one Chemical compound O=C1OC(C(C)(C)C)=NN1C1=CC(OCC#C)=C(Cl)C=C1Cl DVOODWOZJVJKQR-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
- OEYOMNZEMCPTKN-UHFFFAOYSA-N Butamifos Chemical compound CCC(C)NP(=S)(OCC)OC1=CC(C)=CC=C1[N+]([O-])=O OEYOMNZEMCPTKN-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
- VYNOULHXXDFBLU-UHFFFAOYSA-N Cumyluron Chemical compound C=1C=CC=CC=1C(C)(C)NC(=O)NCC1=CC=CC=C1Cl VYNOULHXXDFBLU-UHFFFAOYSA-N 0.000 claims 1
- OFSLKOLYLQSJPB-UHFFFAOYSA-N Cyclosulfamuron Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)NC=2C(=CC=CC=2)C(=O)C2CC2)=N1 OFSLKOLYLQSJPB-UHFFFAOYSA-N 0.000 claims 1
- IKYICRRUVNIHPP-UHFFFAOYSA-N Dimethametryn Chemical compound CCNC1=NC(NC(C)C(C)C)=NC(SC)=N1 IKYICRRUVNIHPP-UHFFFAOYSA-N 0.000 claims 1
- BXEHUCNTIZGSOJ-UHFFFAOYSA-N Esprocarb Chemical compound CC(C)C(C)N(CC)C(=O)SCC1=CC=CC=C1 BXEHUCNTIZGSOJ-UHFFFAOYSA-N 0.000 claims 1
- ICWUMLXQKFTJMH-UHFFFAOYSA-N Etobenzanid Chemical compound C1=CC(OCOCC)=CC=C1C(=O)NC1=CC=CC(Cl)=C1Cl ICWUMLXQKFTJMH-UHFFFAOYSA-N 0.000 claims 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
- NAGRVUXEKKZNHT-UHFFFAOYSA-N Imazosulfuron Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)C=2N3C=CC=CC3=NC=2Cl)=N1 NAGRVUXEKKZNHT-UHFFFAOYSA-N 0.000 claims 1
- SUSRORUBZHMPCO-UHFFFAOYSA-N MC-4379 Chemical compound C1=C([N+]([O-])=O)C(C(=O)OC)=CC(OC=2C(=CC(Cl)=CC=2)Cl)=C1 SUSRORUBZHMPCO-UHFFFAOYSA-N 0.000 claims 1
- CHNUNORXWHYHNE-UHFFFAOYSA-N Oxadiazon Chemical compound C1=C(Cl)C(OC(C)C)=CC(N2C(OC(=N2)C(C)(C)C)=O)=C1Cl CHNUNORXWHYHNE-UHFFFAOYSA-N 0.000 claims 1
- SYJGKVOENHZYMQ-UHFFFAOYSA-N Penoxsulam Chemical compound N1=C2C(OC)=CN=C(OC)N2N=C1NS(=O)(=O)C1=C(OCC(F)F)C=CC=C1C(F)(F)F SYJGKVOENHZYMQ-UHFFFAOYSA-N 0.000 claims 1
- YLPGTOIOYRQOHV-UHFFFAOYSA-N Pretilachlor Chemical compound CCCOCCN(C(=O)CCl)C1=C(CC)C=CC=C1CC YLPGTOIOYRQOHV-UHFFFAOYSA-N 0.000 claims 1
- IHHMUBRVTJMLQO-UHFFFAOYSA-N Pyraclonil Chemical compound C#CCN(C)C1=C(C#N)C=NN1C1=NN(CCCC2)C2=C1Cl IHHMUBRVTJMLQO-UHFFFAOYSA-N 0.000 claims 1
- BGNQYGRXEXDAIQ-UHFFFAOYSA-N Pyrazosulfuron-ethyl Chemical compound C1=NN(C)C(S(=O)(=O)NC(=O)NC=2N=C(OC)C=C(OC)N=2)=C1C(=O)OCC BGNQYGRXEXDAIQ-UHFFFAOYSA-N 0.000 claims 1
- RRKHIAYNPVQKEF-UHFFFAOYSA-N Pyriftalid Chemical compound COC1=CC(OC)=NC(SC=2C=3C(=O)OC(C)C=3C=CC=2)=N1 RRKHIAYNPVQKEF-UHFFFAOYSA-N 0.000 claims 1
- WHKUVVPPKQRRBV-UHFFFAOYSA-N Trasan Chemical compound CC1=CC(Cl)=CC=C1OCC(O)=O WHKUVVPPKQRRBV-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
- ZOMSMJKLGFBRBS-UHFFFAOYSA-N bentazone Chemical compound C1=CC=C2NS(=O)(=O)N(C(C)C)C(=O)C2=C1 ZOMSMJKLGFBRBS-UHFFFAOYSA-N 0.000 claims 1
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims 1
- FUHMZYWBSHTEDZ-UHFFFAOYSA-M bispyribac-sodium Chemical compound [Na+].COC1=CC(OC)=NC(OC=2C(=C(OC=3N=C(OC)C=C(OC)N=3)C=CC=2)C([O-])=O)=N1 FUHMZYWBSHTEDZ-UHFFFAOYSA-M 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
- PQROLKNPFDDLPB-UHFFFAOYSA-N ethyl 2-(4-chloro-2-methylphenoxy)butanoate Chemical compound CCOC(=O)C(CC)OC1=CC=C(Cl)C=C1C PQROLKNPFDDLPB-UHFFFAOYSA-N 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
- DEDOPGXGGQYYMW-UHFFFAOYSA-N molinate Chemical compound CCSC(=O)N1CCCCCC1 DEDOPGXGGQYYMW-UHFFFAOYSA-N 0.000 claims 1
- 125000004043 oxo group Chemical group O=* 0.000 claims 1
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 claims 1
- 125000003170 phenylsulfonyl group Chemical group C1(=CC=CC=C1)S(=O)(=O)* 0.000 claims 1
- LFULEKSKNZEWOE-UHFFFAOYSA-N propanil Chemical compound CCC(=O)NC1=CC=C(Cl)C(Cl)=C1 LFULEKSKNZEWOE-UHFFFAOYSA-N 0.000 claims 1
- 150000003839 salts Chemical class 0.000 claims 1
- MGLWZSOBALDPEK-UHFFFAOYSA-N simetryn Chemical compound CCNC1=NC(NCC)=NC(SC)=N1 MGLWZSOBALDPEK-UHFFFAOYSA-N 0.000 claims 1
- 159000000000 sodium salts Chemical class 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 |
|---|---|---|---|
| JP2004035796A JP4580171B2 (ja) | 2003-02-13 | 2004-02-12 | 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 |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2003035155 | 2003-02-13 | ||
| JP2004035796A JP4580171B2 (ja) | 2003-02-13 | 2004-02-12 | 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 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2004262935A JP2004262935A (ja) | 2004-09-24 |
| JP2004262935A5 true JP2004262935A5 (cg-RX-API-DMAC7.html) | 2007-04-12 |
| JP4580171B2 JP4580171B2 (ja) | 2010-11-10 |
Family
ID=33133937
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2004035796A Expired - Lifetime JP4580171B2 (ja) | 2003-02-13 | 2004-02-12 | 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 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP4580171B2 (cg-RX-API-DMAC7.html) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4580175B2 (ja) * | 2003-02-13 | 2010-11-10 | 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剤組成物 |
| JP5040383B2 (ja) * | 2006-03-17 | 2012-10-03 | 住友化学株式会社 | ピリダジノン化合物及びそれを含有する除草剤 |
| 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 |
| AR064962A1 (es) * | 2007-01-22 | 2009-05-06 | Syngenta Participations Ag | Derivados de piridazina utiles como fungicidas |
| JP5353120B2 (ja) * | 2007-09-14 | 2013-11-27 | 住友化学株式会社 | 除草用組成物 |
| 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 |
| JP5553683B2 (ja) * | 2009-05-29 | 2014-07-16 | 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 |
| JP6029995B2 (ja) * | 2013-02-04 | 2016-11-24 | クミアイ化学工業株式会社 | 除草剤組成物 |
| CN105004833B (zh) * | 2015-05-25 | 2018-07-03 | 贵州百灵企业集团制药股份有限公司 | 一种治疗急性痛风性关节炎、痛风的中药制剂的检测方法 |
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
- 2004-02-12 JP JP2004035796A patent/JP4580171B2/ja not_active Expired - Lifetime
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