JP2009132681A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2009132681A5 JP2009132681A5 JP2008264385A JP2008264385A JP2009132681A5 JP 2009132681 A5 JP2009132681 A5 JP 2009132681A5 JP 2008264385 A JP2008264385 A JP 2008264385A JP 2008264385 A JP2008264385 A JP 2008264385A JP 2009132681 A5 JP2009132681 A5 JP 2009132681A5
- Authority
- JP
- Japan
- Prior art keywords
- methyl
- compounds
- trifluoromethyl
- dimethyl
- compound
- 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
Links
- -1 guanidine series Compound Chemical class 0.000 claims 41
- XAKBSHICSHRJCL-UHFFFAOYSA-N [CH2]C(=O)C1=CC=CC=C1 Chemical group [CH2]C(=O)C1=CC=CC=C1 XAKBSHICSHRJCL-UHFFFAOYSA-N 0.000 claims 11
- 150000001875 compounds Chemical class 0.000 claims 9
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 claims 6
- 230000000844 anti-bacterial effect Effects 0.000 claims 6
- 241000233866 Fungi Species 0.000 claims 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 4
- 125000000217 alkyl group Chemical group 0.000 claims 3
- 125000000623 heterocyclic group Chemical group 0.000 claims 3
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 3
- 229910052717 sulfur Inorganic materials 0.000 claims 3
- ZMYFCFLJBGAQRS-IRXDYDNUSA-N (2R,3S)-epoxiconazole Chemical compound C1=CC(F)=CC=C1[C@@]1(CN2N=CN=C2)[C@H](C=2C(=CC=CC=2)Cl)O1 ZMYFCFLJBGAQRS-IRXDYDNUSA-N 0.000 claims 2
- RYAUSSKQMZRMAI-ALOPSCKCSA-N (2S,6R)-4-[3-(4-tert-butylphenyl)-2-methylpropyl]-2,6-dimethylmorpholine Chemical compound C=1C=C(C(C)(C)C)C=CC=1CC(C)CN1C[C@H](C)O[C@H](C)C1 RYAUSSKQMZRMAI-ALOPSCKCSA-N 0.000 claims 2
- LDVVMCZRFWMZSG-OLQVQODUSA-N (3ar,7as)-2-(trichloromethylsulfanyl)-3a,4,7,7a-tetrahydroisoindole-1,3-dione Chemical compound C1C=CC[C@H]2C(=O)N(SC(Cl)(Cl)Cl)C(=O)[C@H]21 LDVVMCZRFWMZSG-OLQVQODUSA-N 0.000 claims 2
- QNBTYORWCCMPQP-JXAWBTAJSA-N (Z)-dimethomorph Chemical compound C1=C(OC)C(OC)=CC=C1C(\C=1C=CC(Cl)=CC=1)=C/C(=O)N1CCOCC1 QNBTYORWCCMPQP-JXAWBTAJSA-N 0.000 claims 2
- IKNXXTIMVROREQ-WXXKFALUSA-N (e)-but-2-enedioic acid;[2-[3-(4-chlorophenyl)propyl]-2,4,4-trimethyl-1,3-oxazolidin-3-yl]-imidazol-1-ylmethanone Chemical compound OC(=O)\C=C\C(O)=O.C1=CN=CN1C(=O)N1C(C)(C)COC1(C)CCCC1=CC=C(Cl)C=C1.C1=CN=CN1C(=O)N1C(C)(C)COC1(C)CCCC1=CC=C(Cl)C=C1 IKNXXTIMVROREQ-WXXKFALUSA-N 0.000 claims 2
- PXMNMQRDXWABCY-UHFFFAOYSA-N 1-(4-chlorophenyl)-4,4-dimethyl-3-(1H-1,2,4-triazol-1-ylmethyl)pentan-3-ol Chemical compound C1=NC=NN1CC(O)(C(C)(C)C)CCC1=CC=C(Cl)C=C1 PXMNMQRDXWABCY-UHFFFAOYSA-N 0.000 claims 2
- QYZMQZAXGJHGKK-UHFFFAOYSA-N 1-(6-tert-butyl-8-fluoro-2,3-dimethylquinolin-4-yl)ethanone Chemical compound C1=C(C(C)(C)C)C=C2C(C(=O)C)=C(C)C(C)=NC2=C1F QYZMQZAXGJHGKK-UHFFFAOYSA-N 0.000 claims 2
- LQDARGUHUSPFNL-UHFFFAOYSA-N 1-[2-(2,4-dichlorophenyl)-3-(1,1,2,2-tetrafluoroethoxy)propyl]1,2,4-triazole Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(COC(F)(F)C(F)F)CN1C=NC=N1 LQDARGUHUSPFNL-UHFFFAOYSA-N 0.000 claims 2
- MGNFYQILYYYUBS-UHFFFAOYSA-N 1-[3-(4-tert-butylphenyl)-2-methylpropyl]piperidine Chemical compound C=1C=C(C(C)(C)C)C=CC=1CC(C)CN1CCCCC1 MGNFYQILYYYUBS-UHFFFAOYSA-N 0.000 claims 2
- ZVXKYWHJBYIYNI-UHFFFAOYSA-N 1h-pyrazole-4-carboxamide Chemical compound NC(=O)C=1C=NNC=1 ZVXKYWHJBYIYNI-UHFFFAOYSA-N 0.000 claims 2
- NIOPZPCMRQGZCE-WEVVVXLNSA-N 2,4-dinitro-6-(octan-2-yl)phenyl (E)-but-2-enoate Chemical compound CCCCCCC(C)C1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1OC(=O)\C=C\C NIOPZPCMRQGZCE-WEVVVXLNSA-N 0.000 claims 2
- STMIIPIFODONDC-UHFFFAOYSA-N 2-(2,4-dichlorophenyl)-1-(1H-1,2,4-triazol-1-yl)hexan-2-ol Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(O)(CCCC)CN1C=NC=N1 STMIIPIFODONDC-UHFFFAOYSA-N 0.000 claims 2
- UFNOUKDBUJZYDE-UHFFFAOYSA-N 2-(4-chlorophenyl)-3-cyclopropyl-1-(1H-1,2,4-triazol-1-yl)butan-2-ol Chemical compound C1=NC=NN1CC(O)(C=1C=CC(Cl)=CC=1)C(C)C1CC1 UFNOUKDBUJZYDE-UHFFFAOYSA-N 0.000 claims 2
- MNHVNIJQQRJYDH-UHFFFAOYSA-N 2-[2-(1-chlorocyclopropyl)-3-(2-chlorophenyl)-2-hydroxypropyl]-1,2-dihydro-1,2,4-triazole-3-thione Chemical compound N1=CNC(=S)N1CC(C1(Cl)CC1)(O)CC1=CC=CC=C1Cl MNHVNIJQQRJYDH-UHFFFAOYSA-N 0.000 claims 2
- ASMNSUBMNZQTTG-UHFFFAOYSA-N 5-chloro-7-(4-methylpiperidin-1-yl)-6-(2,4,6-trifluorophenyl)-[1,2,4]triazolo[1,5-a]pyrimidine Chemical compound C1CC(C)CCN1C1=C(C=2C(=CC(F)=CC=2F)F)C(Cl)=NC2=NC=NN12 ASMNSUBMNZQTTG-UHFFFAOYSA-N 0.000 claims 2
- 239000005730 Azoxystrobin Substances 0.000 claims 2
- 239000005745 Captan Substances 0.000 claims 2
- 239000005747 Chlorothalonil Substances 0.000 claims 2
- JJLJMEJHUUYSSY-UHFFFAOYSA-L Copper hydroxide Chemical compound [OH-].[OH-].[Cu+2] JJLJMEJHUUYSSY-UHFFFAOYSA-L 0.000 claims 2
- 239000005757 Cyproconazole Substances 0.000 claims 2
- 239000005761 Dimethomorph Substances 0.000 claims 2
- 239000005762 Dimoxystrobin Substances 0.000 claims 2
- 239000005767 Epoxiconazole Substances 0.000 claims 2
- 239000005777 Fenpropidin Substances 0.000 claims 2
- 239000005778 Fenpropimorph Substances 0.000 claims 2
- 239000005780 Fluazinam Substances 0.000 claims 2
- 239000005781 Fludioxonil Substances 0.000 claims 2
- 239000005786 Flutolanil Substances 0.000 claims 2
- 239000005867 Iprodione Substances 0.000 claims 2
- 239000005805 Mepanipyrim Substances 0.000 claims 2
- 239000005806 Meptyldinocap Substances 0.000 claims 2
- 239000005868 Metconazole Substances 0.000 claims 2
- 229930182764 Polyoxin Natural products 0.000 claims 2
- 239000005819 Potassium phosphonate Substances 0.000 claims 2
- MKIMSXGUTQTKJU-UHFFFAOYSA-N Propamocarb hydrochloride Chemical compound [Cl-].CCCOC(=O)NCCC[NH+](C)C MKIMSXGUTQTKJU-UHFFFAOYSA-N 0.000 claims 2
- 239000005825 Prothioconazole Substances 0.000 claims 2
- 239000005869 Pyraclostrobin Substances 0.000 claims 2
- 239000005837 Spiroxamine Substances 0.000 claims 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 2
- 239000005839 Tebuconazole Substances 0.000 claims 2
- 239000005840 Tetraconazole Substances 0.000 claims 2
- 239000005842 Thiophanate-methyl Substances 0.000 claims 2
- 239000005858 Triflumizole Substances 0.000 claims 2
- KKJKGRYXBURLSH-UHFFFAOYSA-N [2-chloro-5-methoxy-3-(trifluoromethyl)pyridin-4-yl]-(2,3,4-trimethoxy-6-methylphenyl)methanone Chemical compound COC1=CN=C(Cl)C(C(F)(F)F)=C1C(=O)C1=C(C)C=C(OC)C(OC)=C1OC KKJKGRYXBURLSH-UHFFFAOYSA-N 0.000 claims 2
- WFDXOXNFNRHQEC-GHRIWEEISA-N azoxystrobin Chemical compound CO\C=C(\C(=O)OC)C1=CC=CC=C1OC1=CC(OC=2C(=CC=CC=2)C#N)=NC=N1 WFDXOXNFNRHQEC-GHRIWEEISA-N 0.000 claims 2
- OIPMQULDKWSNGX-UHFFFAOYSA-N bis[[ethoxy(oxo)phosphaniumyl]oxy]alumanyloxy-ethoxy-oxophosphanium Chemical compound [Al+3].CCO[P+]([O-])=O.CCO[P+]([O-])=O.CCO[P+]([O-])=O OIPMQULDKWSNGX-UHFFFAOYSA-N 0.000 claims 2
- 229940117949 captan Drugs 0.000 claims 2
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims 2
- CRQQGFGUEAVUIL-UHFFFAOYSA-N chlorothalonil Chemical compound ClC1=C(Cl)C(C#N)=C(Cl)C(C#N)=C1Cl CRQQGFGUEAVUIL-UHFFFAOYSA-N 0.000 claims 2
- ORTQZVOHEJQUHG-UHFFFAOYSA-L copper(II) chloride Chemical compound Cl[Cu]Cl ORTQZVOHEJQUHG-UHFFFAOYSA-L 0.000 claims 2
- ACMXQHFNODYQAT-UHFFFAOYSA-N cyflufenamid Chemical compound FC1=CC=C(C(F)(F)F)C(C(NOCC2CC2)=NC(=O)CC=2C=CC=CC=2)=C1F ACMXQHFNODYQAT-UHFFFAOYSA-N 0.000 claims 2
- WXUZAHCNPWONDH-DYTRJAOYSA-N dimoxystrobin Chemical compound CNC(=O)C(=N\OC)\C1=CC=CC=C1COC1=CC(C)=CC=C1C WXUZAHCNPWONDH-DYTRJAOYSA-N 0.000 claims 2
- YXXXKCDYKKSZHL-UHFFFAOYSA-M dipotassium;dioxido(oxo)phosphanium Chemical compound [K+].[K+].[O-][P+]([O-])=O YXXXKCDYKKSZHL-UHFFFAOYSA-M 0.000 claims 2
- VDLGAVXLJYLFDH-UHFFFAOYSA-N fenhexamid Chemical compound C=1C=C(O)C(Cl)=C(Cl)C=1NC(=O)C1(C)CCCCC1 VDLGAVXLJYLFDH-UHFFFAOYSA-N 0.000 claims 2
- UZCGKGPEKUCDTF-UHFFFAOYSA-N fluazinam Chemical compound [O-][N+](=O)C1=CC(C(F)(F)F)=C(Cl)C([N+]([O-])=O)=C1NC1=NC=C(C(F)(F)F)C=C1Cl UZCGKGPEKUCDTF-UHFFFAOYSA-N 0.000 claims 2
- MUJOIMFVNIBMKC-UHFFFAOYSA-N fludioxonil Chemical compound C=12OC(F)(F)OC2=CC=CC=1C1=CNC=C1C#N MUJOIMFVNIBMKC-UHFFFAOYSA-N 0.000 claims 2
- PTCGDEVVHUXTMP-UHFFFAOYSA-N flutolanil Chemical compound CC(C)OC1=CC=CC(NC(=O)C=2C(=CC=CC=2)C(F)(F)F)=C1 PTCGDEVVHUXTMP-UHFFFAOYSA-N 0.000 claims 2
- 229910052736 halogen Inorganic materials 0.000 claims 2
- 125000005843 halogen group Chemical group 0.000 claims 2
- ONUFESLQCSAYKA-UHFFFAOYSA-N iprodione Chemical compound O=C1N(C(=O)NC(C)C)CC(=O)N1C1=CC(Cl)=CC(Cl)=C1 ONUFESLQCSAYKA-UHFFFAOYSA-N 0.000 claims 2
- PVTHJAPFENJVNC-MHRBZPPQSA-N kasugamycin Chemical compound N[C@H]1C[C@H](NC(=N)C(O)=O)[C@@H](C)O[C@@H]1O[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@H](O)[C@@H]1O PVTHJAPFENJVNC-MHRBZPPQSA-N 0.000 claims 2
- CIFWZNRJIBNXRE-UHFFFAOYSA-N mepanipyrim Chemical compound CC#CC1=CC(C)=NC(NC=2C=CC=CC=2)=N1 CIFWZNRJIBNXRE-UHFFFAOYSA-N 0.000 claims 2
- XWPZUHJBOLQNMN-UHFFFAOYSA-N metconazole Chemical compound C1=NC=NN1CC1(O)C(C)(C)CCC1CC1=CC=C(Cl)C=C1 XWPZUHJBOLQNMN-UHFFFAOYSA-N 0.000 claims 2
- YEBIHIICWDDQOL-YBHNRIQQSA-N polyoxin Polymers O[C@@H]1[C@H](O)[C@@H](C(C=O)N)O[C@H]1N1C(=O)NC(=O)C(C(O)=O)=C1 YEBIHIICWDDQOL-YBHNRIQQSA-N 0.000 claims 2
- 229910000028 potassium bicarbonate Inorganic materials 0.000 claims 2
- 239000011736 potassium bicarbonate Substances 0.000 claims 2
- 235000015497 potassium bicarbonate Nutrition 0.000 claims 2
- TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 claims 2
- TVLSRXXIMLFWEO-UHFFFAOYSA-N prochloraz Chemical compound C1=CN=CN1C(=O)N(CCC)CCOC1=C(Cl)C=C(Cl)C=C1Cl TVLSRXXIMLFWEO-UHFFFAOYSA-N 0.000 claims 2
- QXJKBPAVAHBARF-BETUJISGSA-N procymidone Chemical compound O=C([C@]1(C)C[C@@]1(C1=O)C)N1C1=CC(Cl)=CC(Cl)=C1 QXJKBPAVAHBARF-BETUJISGSA-N 0.000 claims 2
- HZRSNVGNWUDEFX-UHFFFAOYSA-N pyraclostrobin Chemical compound COC(=O)N(OC)C1=CC=CC=C1COC1=NN(C=2C=CC(Cl)=CC=2)C=C1 HZRSNVGNWUDEFX-UHFFFAOYSA-N 0.000 claims 2
- CRFYLQMIDWBKRT-LPYMAVHISA-N pyribencarb Chemical compound C1=C(Cl)C(CNC(=O)OC)=CC(C(\C)=N\OCC=2N=C(C)C=CC=2)=C1 CRFYLQMIDWBKRT-LPYMAVHISA-N 0.000 claims 2
- NMVCBWZLCXANER-UHFFFAOYSA-N pyriofenone Chemical compound COC1=C(OC)C(OC)=CC(C)=C1C(=O)C1=C(C)C(Cl)=CN=C1OC NMVCBWZLCXANER-UHFFFAOYSA-N 0.000 claims 2
- 150000003839 salts Chemical class 0.000 claims 2
- PUYXTUJWRLOUCW-UHFFFAOYSA-N spiroxamine Chemical compound O1C(CN(CC)CCC)COC11CCC(C(C)(C)C)CC1 PUYXTUJWRLOUCW-UHFFFAOYSA-N 0.000 claims 2
- 239000011593 sulfur Substances 0.000 claims 2
- QGHREAKMXXNCOA-UHFFFAOYSA-N thiophanate-methyl Chemical group COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC QGHREAKMXXNCOA-UHFFFAOYSA-N 0.000 claims 2
- DQJCHOQLCLEDLL-UHFFFAOYSA-N tricyclazole Chemical compound CC1=CC=CC2=C1N1C=NN=C1S2 DQJCHOQLCLEDLL-UHFFFAOYSA-N 0.000 claims 2
- 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 claims 2
- 125000004641 (C1-C12) haloalkyl group Chemical group 0.000 claims 1
- BKBSMMUEEAWFRX-NBVRZTHBSA-N (E)-flumorph Chemical compound C1=C(OC)C(OC)=CC=C1C(\C=1C=CC(F)=CC=1)=C\C(=O)N1CCOCC1 BKBSMMUEEAWFRX-NBVRZTHBSA-N 0.000 claims 1
- WKBPZYKAUNRMKP-UHFFFAOYSA-N 1-[2-(2,4-dichlorophenyl)pentyl]1,2,4-triazole Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(CCC)CN1C=NC=N1 WKBPZYKAUNRMKP-UHFFFAOYSA-N 0.000 claims 1
- YIKWKLYQRFRGPM-UHFFFAOYSA-N 1-dodecylguanidine acetate Chemical compound CC(O)=O.CCCCCCCCCCCCN=C(N)N YIKWKLYQRFRGPM-UHFFFAOYSA-N 0.000 claims 1
- PFFIDZXUXFLSSR-UHFFFAOYSA-N 1-methyl-N-[2-(4-methylpentan-2-yl)-3-thienyl]-3-(trifluoromethyl)pyrazole-4-carboxamide Chemical compound S1C=CC(NC(=O)C=2C(=NN(C)C=2)C(F)(F)F)=C1C(C)CC(C)C PFFIDZXUXFLSSR-UHFFFAOYSA-N 0.000 claims 1
- KAESVJOAVNADME-UHFFFAOYSA-N 1H-pyrrole Natural products C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 claims 1
- AVRPFRMDMNDIDH-UHFFFAOYSA-N 1h-quinazolin-2-one Chemical class C1=CC=CC2=NC(O)=NC=C21 AVRPFRMDMNDIDH-UHFFFAOYSA-N 0.000 claims 1
- YTOPFCCWCSOHFV-UHFFFAOYSA-N 2,6-dimethyl-4-tridecylmorpholine Chemical compound CCCCCCCCCCCCCN1CC(C)OC(C)C1 YTOPFCCWCSOHFV-UHFFFAOYSA-N 0.000 claims 1
- ATRQECRSCHYSNP-UHFFFAOYSA-N 2-(trifluoromethyl)pyridine Chemical compound FC(F)(F)C1=CC=CC=N1 ATRQECRSCHYSNP-UHFFFAOYSA-N 0.000 claims 1
- 125000004204 2-methoxyphenyl group Chemical group [H]C1=C([H])C(*)=C(OC([H])([H])[H])C([H])=C1[H] 0.000 claims 1
- IWTFOFMTUOBLHG-UHFFFAOYSA-N 2-methoxypyridine Chemical compound COC1=CC=CC=N1 IWTFOFMTUOBLHG-UHFFFAOYSA-N 0.000 claims 1
- SOUGWDPPRBKJEX-UHFFFAOYSA-N 3,5-dichloro-N-(1-chloro-3-methyl-2-oxopentan-3-yl)-4-methylbenzamide Chemical compound ClCC(=O)C(C)(CC)NC(=O)C1=CC(Cl)=C(C)C(Cl)=C1 SOUGWDPPRBKJEX-UHFFFAOYSA-N 0.000 claims 1
- FSCWZHGZWWDELK-UHFFFAOYSA-N 3-(3,5-dichlorophenyl)-5-ethenyl-5-methyl-2,4-oxazolidinedione Chemical compound O=C1C(C)(C=C)OC(=O)N1C1=CC(Cl)=CC(Cl)=C1 FSCWZHGZWWDELK-UHFFFAOYSA-N 0.000 claims 1
- RQDJADAKIFFEKQ-UHFFFAOYSA-N 4-(4-chlorophenyl)-2-phenyl-2-(1,2,4-triazol-1-ylmethyl)butanenitrile Chemical compound C1=CC(Cl)=CC=C1CCC(C=1C=CC=CC=1)(C#N)CN1N=CN=C1 RQDJADAKIFFEKQ-UHFFFAOYSA-N 0.000 claims 1
- KJTRXVXWSSPHRV-UHFFFAOYSA-N 4-benzoyl-5-methyl-2-phenyl-1h-pyrazol-3-one Chemical compound O=C1C(C(=O)C=2C=CC=CC=2)=C(C)NN1C1=CC=CC=C1 KJTRXVXWSSPHRV-UHFFFAOYSA-N 0.000 claims 1
- 125000002373 5 membered heterocyclic group Chemical group 0.000 claims 1
- 125000004070 6 membered heterocyclic group Chemical group 0.000 claims 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N Acrylic acid Chemical compound OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims 1
- 239000005727 Amisulbrom Substances 0.000 claims 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 claims 1
- 239000005740 Boscalid Substances 0.000 claims 1
- FERIUCNNQQJTOY-UHFFFAOYSA-M Butyrate Chemical compound CCCC([O-])=O FERIUCNNQQJTOY-UHFFFAOYSA-M 0.000 claims 1
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Natural products CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 claims 1
- TWFZGCMQGLPBSX-UHFFFAOYSA-N Carbendazim Natural products C1=CC=C2NC(NC(=O)OC)=NC2=C1 TWFZGCMQGLPBSX-UHFFFAOYSA-N 0.000 claims 1
- 239000005746 Carboxin Substances 0.000 claims 1
- 235000008733 Citrus aurantifolia Nutrition 0.000 claims 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims 1
- 239000005749 Copper compound Substances 0.000 claims 1
- 239000005760 Difenoconazole Substances 0.000 claims 1
- 239000005765 Dodemorph Substances 0.000 claims 1
- 241001522296 Erithacus rubecula Species 0.000 claims 1
- 239000005775 Fenbuconazole Substances 0.000 claims 1
- 239000005784 Fluoxastrobin Substances 0.000 claims 1
- 239000005785 Fluquinconazole Substances 0.000 claims 1
- 239000005796 Ipconazole Substances 0.000 claims 1
- 239000005797 Iprovalicarb Substances 0.000 claims 1
- NWUWYYSKZYIQAE-ZBFHGGJFSA-N L-(R)-iprovalicarb Chemical compound CC(C)OC(=O)N[C@@H](C(C)C)C(=O)N[C@H](C)C1=CC=C(C)C=C1 NWUWYYSKZYIQAE-ZBFHGGJFSA-N 0.000 claims 1
- 241000907681 Morpho Species 0.000 claims 1
- 239000005813 Penconazole Substances 0.000 claims 1
- 239000005816 Penthiopyrad Substances 0.000 claims 1
- 239000005818 Picoxystrobin Substances 0.000 claims 1
- 239000005822 Propiconazole Substances 0.000 claims 1
- 239000005823 Propineb Substances 0.000 claims 1
- 239000005835 Silthiofam Substances 0.000 claims 1
- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 claims 1
- 229930182692 Strobilurin Natural products 0.000 claims 1
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 claims 1
- 235000011941 Tilia x europaea Nutrition 0.000 claims 1
- 239000005857 Trifloxystrobin Substances 0.000 claims 1
- 229930195482 Validamycin Natural products 0.000 claims 1
- 239000005863 Zoxamide Substances 0.000 claims 1
- ZHBRLEQONSVJJN-UHFFFAOYSA-N [2,5-dichloro-3-(trifluoromethyl)pyridin-4-yl]-(2,3,4-trimethoxy-6-methylphenyl)methanone Chemical compound COC1=C(OC)C(OC)=CC(C)=C1C(=O)C1=C(Cl)C=NC(Cl)=C1C(F)(F)F ZHBRLEQONSVJJN-UHFFFAOYSA-N 0.000 claims 1
- BREATYVWRHIPIY-UHFFFAOYSA-N amisulbrom Chemical compound CN(C)S(=O)(=O)N1C=NC(S(=O)(=O)N2C3=CC(F)=CC=C3C(Br)=C2C)=N1 BREATYVWRHIPIY-UHFFFAOYSA-N 0.000 claims 1
- 239000003242 anti bacterial agent Substances 0.000 claims 1
- 229940088710 antibiotic agent Drugs 0.000 claims 1
- 125000004429 atom Chemical group 0.000 claims 1
- RIOXQFHNBCKOKP-UHFFFAOYSA-N benomyl Chemical compound C1=CC=C2N(C(=O)NCCCC)C(NC(=O)OC)=NC2=C1 RIOXQFHNBCKOKP-UHFFFAOYSA-N 0.000 claims 1
- 150000008366 benzophenones Chemical class 0.000 claims 1
- MITFXPHMIHQXPI-UHFFFAOYSA-N benzoxaprofen Natural products N=1C2=CC(C(C(O)=O)C)=CC=C2OC=1C1=CC=C(Cl)C=C1 MITFXPHMIHQXPI-UHFFFAOYSA-N 0.000 claims 1
- LDLMOOXUCMHBMZ-UHFFFAOYSA-N bixafen Chemical compound FC(F)C1=NN(C)C=C1C(=O)NC1=CC=C(F)C=C1C1=CC=C(Cl)C(Cl)=C1 LDLMOOXUCMHBMZ-UHFFFAOYSA-N 0.000 claims 1
- WYEMLYFITZORAB-UHFFFAOYSA-N boscalid Chemical compound C1=CC(Cl)=CC=C1C1=CC=CC=C1NC(=O)C1=CC=CN=C1Cl WYEMLYFITZORAB-UHFFFAOYSA-N 0.000 claims 1
- 229940118790 boscalid Drugs 0.000 claims 1
- 150000004657 carbamic acid derivatives Chemical class 0.000 claims 1
- 239000006013 carbendazim Substances 0.000 claims 1
- JNPZQRQPIHJYNM-UHFFFAOYSA-N carbendazim Chemical compound C1=C[CH]C2=NC(NC(=O)OC)=NC2=C1 JNPZQRQPIHJYNM-UHFFFAOYSA-N 0.000 claims 1
- GYSSRZJIHXQEHQ-UHFFFAOYSA-N carboxin Chemical compound S1CCOC(C)=C1C(=O)NC1=CC=CC=C1 GYSSRZJIHXQEHQ-UHFFFAOYSA-N 0.000 claims 1
- 239000010949 copper Substances 0.000 claims 1
- 229910052802 copper Inorganic materials 0.000 claims 1
- 150000001880 copper compounds Chemical class 0.000 claims 1
- 229910000365 copper sulfate Inorganic materials 0.000 claims 1
- ARUVKPQLZAKDPS-UHFFFAOYSA-L copper(II) sulfate Chemical compound [Cu+2].[O-][S+2]([O-])([O-])[O-] ARUVKPQLZAKDPS-UHFFFAOYSA-L 0.000 claims 1
- DGJMPUGMZIKDRO-UHFFFAOYSA-N cyanoacetamide Chemical class NC(=O)CC#N DGJMPUGMZIKDRO-UHFFFAOYSA-N 0.000 claims 1
- 150000008056 dicarboxyimides Chemical class 0.000 claims 1
- BQYJATMQXGBDHF-UHFFFAOYSA-N difenoconazole Chemical compound O1C(C)COC1(C=1C(=CC(OC=2C=CC(Cl)=CC=2)=CC=1)Cl)CN1N=CN=C1 BQYJATMQXGBDHF-UHFFFAOYSA-N 0.000 claims 1
- 125000001028 difluoromethyl group Chemical group [H]C(F)(F)* 0.000 claims 1
- FBOUIAKEJMZPQG-BLXFFLACSA-N diniconazole-M Chemical compound C1=NC=NN1/C([C@H](O)C(C)(C)C)=C/C1=CC=C(Cl)C=C1Cl FBOUIAKEJMZPQG-BLXFFLACSA-N 0.000 claims 1
- 150000005182 dinitrobenzenes Chemical class 0.000 claims 1
- 239000012990 dithiocarbamate Substances 0.000 claims 1
- JMXKCYUTURMERF-UHFFFAOYSA-N dodemorph Chemical compound C1C(C)OC(C)CN1C1CCCCCCCCCCC1 JMXKCYUTURMERF-UHFFFAOYSA-N 0.000 claims 1
- AWZOLILCOUMRDG-UHFFFAOYSA-N edifenphos Chemical compound C=1C=CC=CC=1SP(=O)(OCC)SC1=CC=CC=C1 AWZOLILCOUMRDG-UHFFFAOYSA-N 0.000 claims 1
- DWRKFAJEBUWTQM-UHFFFAOYSA-N etaconazole Chemical compound O1C(CC)COC1(C=1C(=CC(Cl)=CC=1)Cl)CN1N=CN=C1 DWRKFAJEBUWTQM-UHFFFAOYSA-N 0.000 claims 1
- KVDJTXBXMWJJEF-UHFFFAOYSA-N fluopyram Chemical compound ClC1=CC(C(F)(F)F)=CN=C1CCNC(=O)C1=CC=CC=C1C(F)(F)F KVDJTXBXMWJJEF-UHFFFAOYSA-N 0.000 claims 1
- UFEODZBUAFNAEU-NLRVBDNBSA-N fluoxastrobin Chemical compound C=1C=CC=C(OC=2C(=C(OC=3C(=CC=CC=3)Cl)N=CN=2)F)C=1C(=N/OC)\C1=NOCCO1 UFEODZBUAFNAEU-NLRVBDNBSA-N 0.000 claims 1
- IJJVMEJXYNJXOJ-UHFFFAOYSA-N fluquinconazole Chemical compound C=1C=C(Cl)C=C(Cl)C=1N1C(=O)C2=CC(F)=CC=C2N=C1N1C=NC=N1 IJJVMEJXYNJXOJ-UHFFFAOYSA-N 0.000 claims 1
- FQKUGOMFVDPBIZ-UHFFFAOYSA-N flusilazole Chemical compound C=1C=C(F)C=CC=1[Si](C=1C=CC(F)=CC=1)(C)CN1C=NC=N1 FQKUGOMFVDPBIZ-UHFFFAOYSA-N 0.000 claims 1
- KGVPNLBXJKTABS-UHFFFAOYSA-N hymexazol Chemical compound CC1=CC(O)=NO1 KGVPNLBXJKTABS-UHFFFAOYSA-N 0.000 claims 1
- AGKSTYPVMZODRV-UHFFFAOYSA-N imibenconazole Chemical compound C1=CC(Cl)=CC=C1CSC(CN1N=CN=C1)=NC1=CC=C(Cl)C=C1Cl AGKSTYPVMZODRV-UHFFFAOYSA-N 0.000 claims 1
- 125000002962 imidazol-1-yl group Chemical group [*]N1C([H])=NC([H])=C1[H] 0.000 claims 1
- QTYCMDBMOLSEAM-UHFFFAOYSA-N ipconazole Chemical compound C1=NC=NN1CC1(O)C(C(C)C)CCC1CC1=CC=C(Cl)C=C1 QTYCMDBMOLSEAM-UHFFFAOYSA-N 0.000 claims 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 1
- 239000004571 lime Substances 0.000 claims 1
- BCTQJXQXJVLSIG-UHFFFAOYSA-N mepronil Chemical compound CC(C)OC1=CC=CC(NC(=O)C=2C(=CC=CC=2)C)=C1 BCTQJXQXJVLSIG-UHFFFAOYSA-N 0.000 claims 1
- SQDFHQJTAWCFIB-UHFFFAOYSA-N n-methylidenehydroxylamine Chemical class ON=C SQDFHQJTAWCFIB-UHFFFAOYSA-N 0.000 claims 1
- 229910052757 nitrogen Inorganic materials 0.000 claims 1
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 1
- 150000004045 organic chlorine compounds Chemical class 0.000 claims 1
- 150000002903 organophosphorus compounds Chemical class 0.000 claims 1
- JHIPUJPTQJYEQK-ZLHHXESBSA-N orysastrobin Chemical compound CNC(=O)C(=N\OC)\C1=CC=CC=C1CO\N=C(/C)\C(=N\OC)\C(\C)=N\OC JHIPUJPTQJYEQK-ZLHHXESBSA-N 0.000 claims 1
- AMEKQAFGQBKLKX-UHFFFAOYSA-N oxycarboxin Chemical compound O=S1(=O)CCOC(C)=C1C(=O)NC1=CC=CC=C1 AMEKQAFGQBKLKX-UHFFFAOYSA-N 0.000 claims 1
- 229910052760 oxygen Inorganic materials 0.000 claims 1
- 125000004430 oxygen atom Chemical group O* 0.000 claims 1
- LKPLKUMXSAEKID-UHFFFAOYSA-N pentachloronitrobenzene Chemical compound [O-][N+](=O)C1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl LKPLKUMXSAEKID-UHFFFAOYSA-N 0.000 claims 1
- GCSHUYKULREZSJ-UHFFFAOYSA-N phenyl(pyridin-2-yl)methanone Chemical class C=1C=CC=NC=1C(=O)C1=CC=CC=C1 GCSHUYKULREZSJ-UHFFFAOYSA-N 0.000 claims 1
- 150000008060 phenylpyrroles Chemical class 0.000 claims 1
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical class OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 claims 1
- IBSNKSODLGJUMQ-SDNWHVSQSA-N picoxystrobin Chemical compound CO\C=C(\C(=O)OC)C1=CC=CC=C1COC1=CC=CC(C(F)(F)F)=N1 IBSNKSODLGJUMQ-SDNWHVSQSA-N 0.000 claims 1
- 150000003053 piperidines Chemical class 0.000 claims 1
- 229920002635 polyurethane Polymers 0.000 claims 1
- WHHIPMZEDGBUCC-UHFFFAOYSA-N probenazole Chemical compound C1=CC=C2C(OCC=C)=NS(=O)(=O)C2=C1 WHHIPMZEDGBUCC-UHFFFAOYSA-N 0.000 claims 1
- STJLVHWMYQXCPB-UHFFFAOYSA-N propiconazole Chemical compound O1C(CCC)COC1(C=1C(=CC(Cl)=CC=1)Cl)CN1N=CN=C1 STJLVHWMYQXCPB-UHFFFAOYSA-N 0.000 claims 1
- KKMLIVYBGSAJPM-UHFFFAOYSA-L propineb Chemical compound [Zn+2].[S-]C(=S)NC(C)CNC([S-])=S KKMLIVYBGSAJPM-UHFFFAOYSA-L 0.000 claims 1
- 125000003226 pyrazolyl group Chemical group 0.000 claims 1
- 125000004076 pyridyl group Chemical group 0.000 claims 1
- 150000003248 quinolines Chemical class 0.000 claims 1
- MXMXHPPIGKYTAR-UHFFFAOYSA-N silthiofam Chemical compound CC=1SC([Si](C)(C)C)=C(C(=O)NCC=C)C=1C MXMXHPPIGKYTAR-UHFFFAOYSA-N 0.000 claims 1
- 235000001508 sulfur Nutrition 0.000 claims 1
- 125000004434 sulfur atom Chemical group 0.000 claims 1
- 150000003464 sulfur compounds Chemical class 0.000 claims 1
- ISIJQEHRDSCQIU-UHFFFAOYSA-N tert-butyl 2,7-diazaspiro[4.5]decane-7-carboxylate Chemical compound C1N(C(=O)OC(C)(C)C)CCCC11CNCC1 ISIJQEHRDSCQIU-UHFFFAOYSA-N 0.000 claims 1
- 239000004308 thiabendazole Substances 0.000 claims 1
- WJCNZQLZVWNLKY-UHFFFAOYSA-N thiabendazole Chemical compound S1C=NC(C=2NC3=CC=CC=C3N=2)=C1 WJCNZQLZVWNLKY-UHFFFAOYSA-N 0.000 claims 1
- 229960004546 thiabendazole Drugs 0.000 claims 1
- 235000010296 thiabendazole Nutrition 0.000 claims 1
- 125000004305 thiazinyl group Chemical group S1NC(=CC=C1)* 0.000 claims 1
- 125000001544 thienyl group Chemical group 0.000 claims 1
- XWKBMOUUGHARTI-UHFFFAOYSA-N tricalcium;diphosphite Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])[O-].[O-]P([O-])[O-] XWKBMOUUGHARTI-UHFFFAOYSA-N 0.000 claims 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 claims 1
- NCPXQVVMIXIKTN-UHFFFAOYSA-N trisodium;phosphite Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])[O-] NCPXQVVMIXIKTN-UHFFFAOYSA-N 0.000 claims 1
- JARYYMUOCXVXNK-IMTORBKUSA-N validamycin 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-IMTORBKUSA-N 0.000 claims 1
- NWONKYPBYAMBJT-UHFFFAOYSA-L zinc sulfate Chemical compound [Zn+2].[O-]S([O-])(=O)=O NWONKYPBYAMBJT-UHFFFAOYSA-L 0.000 claims 1
- 229910000368 zinc sulfate Inorganic materials 0.000 claims 1
- 229960001763 zinc sulfate Drugs 0.000 claims 1
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2008264385A JP5631540B2 (ja) | 2007-11-05 | 2008-10-10 | 殺菌性組成物及び有害菌類の防除方法 |
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2007287699 | 2007-11-05 | ||
| JP2007287699 | 2007-11-05 | ||
| JP2008264385A JP5631540B2 (ja) | 2007-11-05 | 2008-10-10 | 殺菌性組成物及び有害菌類の防除方法 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2009132681A JP2009132681A (ja) | 2009-06-18 |
| JP2009132681A5 true JP2009132681A5 (enExample) | 2011-11-17 |
| JP5631540B2 JP5631540B2 (ja) | 2014-11-26 |
Family
ID=40125610
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2008264385A Active JP5631540B2 (ja) | 2007-11-05 | 2008-10-10 | 殺菌性組成物及び有害菌類の防除方法 |
Country Status (32)
Families Citing this family (28)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB0812028D0 (en) * | 2008-07-01 | 2008-08-06 | Syngenta Participations Ag | Fungicidal compositions |
| WO2010037482A2 (de) * | 2008-10-02 | 2010-04-08 | Bayer Cropscience Aktiengesellschaft | Verwendung von schwefelhaltigen, heteroaromatischen säureanaloga |
| JP5940368B2 (ja) * | 2011-05-24 | 2016-06-29 | 石原産業株式会社 | 殺菌剤組成物及び植物病害の防除方法 |
| CN103749497A (zh) * | 2011-08-18 | 2014-04-30 | 陕西美邦农药有限公司 | 一种含丙硫菌唑的杀菌组合物 |
| JP6005652B2 (ja) * | 2011-09-26 | 2016-10-12 | 日本曹達株式会社 | 農園芸用殺菌剤組成物 |
| PE20142184A1 (es) * | 2011-11-09 | 2014-12-06 | Stockton Israel Ltd | Combinaciones de compuestos antifungicos y aceite del arbol del te para el tratamiento de una planta infectada con oomicetes |
| CA2857464A1 (en) | 2012-01-25 | 2013-08-01 | Sumitomo Chemical Company, Limited | Plant disease control composition |
| JP2013231003A (ja) * | 2012-04-27 | 2013-11-14 | Institute Of Physical & Chemical Research | ブラックシガトカ病害用防除剤 |
| EP3318127A1 (en) * | 2013-09-30 | 2018-05-09 | Basf Se | Compositions comprising khco3 |
| CN106132202B (zh) | 2014-03-20 | 2021-12-31 | 三井化学Agro株式会社 | 植物病害防除组合物及应用该组合物以防除植物病害的方法 |
| RU2567772C1 (ru) * | 2014-11-18 | 2015-11-10 | Акционерное общество "Щелково Агрохим" | Фунгицидная композиция для защиты сельскохозяйственных культур |
| JPWO2016194971A1 (ja) * | 2015-06-01 | 2018-03-15 | 石原産業株式会社 | 殺菌剤組成物及び植物病害の防除方法 |
| KR102317161B1 (ko) | 2016-03-07 | 2021-10-26 | 이시하라 산교 가부시끼가이샤 | 이소페타미드의 식물 병해 방제 효과의 증강 방법 및 식물 병해의 방제 방법 |
| CN106665620A (zh) * | 2016-12-08 | 2017-05-17 | 深圳诺普信农化股份有限公司 | 杀菌组合物 |
| CN106937636A (zh) * | 2017-04-22 | 2017-07-11 | 北京科发伟业农药技术中心 | 含氟唑环菌胺的杀菌组合物 |
| CN107593707A (zh) * | 2017-07-21 | 2018-01-19 | 陕西康禾立丰生物科技药业有限公司 | 一种含异丙噻菌胺的杀菌组合物 |
| MX2020000827A (es) | 2017-07-26 | 2020-10-05 | Nutriag Ltd | Acido de fosforo y composiciones componentes de cobre estabilizadas con alquilamina o alcanolamina para controlar una enfermedad de las plantas causada por un organismo fitopatogenico. |
| CN107347884A (zh) * | 2017-08-31 | 2017-11-17 | 陕西康禾立丰生物科技药业有限公司 | 一种含有异丙噻菌胺的杀菌组合物 |
| CN107549175A (zh) * | 2017-08-31 | 2018-01-09 | 陕西康禾立丰生物科技药业有限公司 | 一种含异丙噻菌胺与三唑类的杀菌组合物 |
| JP2021004176A (ja) * | 2017-09-06 | 2021-01-14 | 石原産業株式会社 | 殺菌剤組成物及び作物の病害防除方法 |
| CN108207974A (zh) * | 2017-12-29 | 2018-06-29 | 广东广康生化科技股份有限公司 | 含灭菌丹和异丙噻菌胺的杀菌组合物及应用 |
| RU2681739C1 (ru) * | 2018-06-21 | 2019-03-12 | Акционерное общество "Щелково Агрохим" | Фунгицидная композиция, обладающая синергетической активностью |
| CN109452298A (zh) * | 2018-12-25 | 2019-03-12 | 陕西上格之路生物科学有限公司 | 一种含有异丙噻菌胺和克菌丹的杀菌组合物 |
| CN109452281A (zh) * | 2018-12-25 | 2019-03-12 | 陕西上格之路生物科学有限公司 | 一种含有异丙噻菌胺和环酰菌胺的杀菌组合物 |
| WO2021082997A1 (zh) * | 2019-10-29 | 2021-05-06 | 沈阳中化农药化工研发有限公司 | 一种含取代苯乙酮结构片段的酰胺类化合物及其制备方法和用途 |
| WO2024046311A1 (zh) * | 2022-08-29 | 2024-03-07 | 江苏中旗科技股份有限公司 | 一种用于杀真菌的组合物及应用组合物的方法 |
| CN119032957A (zh) * | 2023-12-28 | 2024-11-29 | 河北省农林科学院植物保护研究所 | 一种含异丙噻菌胺的杀菌组合物及应用 |
| CN119111537B (zh) * | 2024-09-11 | 2025-10-17 | 陕西西大华特科技实业有限公司 | 一种含有异丙噻菌胺和噻霉酮的杀菌组合物 |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0900021B1 (de) * | 1996-04-26 | 2002-06-19 | Basf Aktiengesellschaft | Fungizide mischung |
| PT1256569E (pt) * | 2000-02-16 | 2010-07-19 | Ishihara Sangyo Kaisha | Derivados de fenacilamina, sua produão e controladores de pragas que contm esses derivados |
| TWI242006B (en) * | 2000-10-23 | 2005-10-21 | Ishihara Sangyo Kaisha | Pesticidal composition |
| CA2460789C (en) | 2001-09-18 | 2011-06-21 | Ishihara Sangyo Kaisha, Ltd. | Acid amide derivatives, process for their production and pesticides containing them |
| JP4300009B2 (ja) * | 2001-09-18 | 2009-07-22 | 石原産業株式会社 | 酸アミド誘導体、それらの製造方法及びそれらを含有する有害生物防除剤 |
| TWI366438B (en) * | 2004-08-12 | 2012-06-21 | Ishihara Sangyo Kaisha | Fungicidal composition containing acid amide derivative |
| JP5173126B2 (ja) * | 2004-08-12 | 2013-03-27 | 石原産業株式会社 | 酸アミド誘導体を含有する殺菌性組成物 |
| JP5068985B2 (ja) * | 2005-12-16 | 2012-11-07 | 石原産業株式会社 | カルボン酸アミド誘導体を含有する殺菌性組成物 |
| JP2007210924A (ja) * | 2006-02-08 | 2007-08-23 | Ishihara Sangyo Kaisha Ltd | カルボン酸アミド誘導体を含有する殺菌性組成物 |
| TWI435863B (zh) * | 2006-03-20 | 2014-05-01 | Nihon Nohyaku Co Ltd | Ｎ-２-（雜）芳基乙基甲醯胺衍生物及含該衍生物之蟲害防治劑 |
-
2008
- 2008-10-10 JP JP2008264385A patent/JP5631540B2/ja active Active
- 2008-10-20 CN CN202211302583.4A patent/CN115606598A/zh active Pending
- 2008-10-20 BR BRPI0819222A patent/BRPI0819222B1/pt active IP Right Grant
- 2008-10-20 HR HRP20171012TT patent/HRP20171012T1/hr unknown
- 2008-10-20 MX MX2010005025A patent/MX2010005025A/es active IP Right Grant
- 2008-10-20 NZ NZ584754A patent/NZ584754A/en unknown
- 2008-10-20 AU AU2008325844A patent/AU2008325844B2/en active Active
- 2008-10-20 CA CA2702825A patent/CA2702825C/en active Active
- 2008-10-20 CN CN202110896054.0A patent/CN113598173B/zh active Active
- 2008-10-20 UA UAA201005499A patent/UA99930C2/ru unknown
- 2008-10-20 PL PL08847581T patent/PL2205096T3/pl unknown
- 2008-10-20 DK DK08847581.9T patent/DK2205096T3/en active
- 2008-10-20 CN CN201610224239.6A patent/CN105851004B/zh active Active
- 2008-10-20 HU HUE08847581A patent/HUE035218T2/hu unknown
- 2008-10-20 CN CN201910057170.6A patent/CN109673644B/zh active Active
- 2008-10-20 CN CN200880114754.2A patent/CN101917858B/zh active Active
- 2008-10-20 BR BR122017000361-5A patent/BR122017000361B1/pt active IP Right Grant
- 2008-10-20 SI SI200831825A patent/SI2205096T1/sl unknown
- 2008-10-20 LT LTEP08847581.9T patent/LT2205096T/lt unknown
- 2008-10-20 WO PCT/JP2008/069392 patent/WO2009060734A2/en not_active Ceased
- 2008-10-20 KR KR1020107009856A patent/KR101527245B1/ko active Active
- 2008-10-20 EP EP08847581.9A patent/EP2205096B1/en active Active
- 2008-10-20 UA UAA201207242A patent/UA110695C2/uk unknown
- 2008-10-20 RU RU2010122898/13A patent/RU2483541C2/ru active
- 2008-10-20 US US12/740,121 patent/US8568755B2/en active Active
- 2008-10-20 NZ NZ599953A patent/NZ599953A/xx unknown
- 2008-10-20 CN CN201410079880.6A patent/CN103918661B/zh active Active
- 2008-10-20 ES ES08847581.9T patent/ES2633288T3/es active Active
- 2008-10-20 PT PT88475819T patent/PT2205096T/pt unknown
- 2008-10-20 RS RS20170608A patent/RS56099B1/sr unknown
- 2008-10-28 TW TW097141354A patent/TWI434650B/zh active
- 2008-10-29 AR ARP080104723A patent/AR069096A1/es active IP Right Grant
- 2008-11-04 CL CL2008003288A patent/CL2008003288A1/es unknown
-
2010
- 2010-04-19 ZA ZA2010/02726A patent/ZA201002726B/en unknown
- 2010-04-29 IL IL205476A patent/IL205476B/en active IP Right Grant
- 2010-04-30 CR CR11408A patent/CR11408A/es unknown
- 2010-04-30 MA MA32808A patent/MA31802B1/fr unknown
- 2010-05-05 CO CO10053460A patent/CO6270288A2/es active IP Right Grant
- 2010-05-05 EC EC2010010157A patent/ECSP10010157A/es unknown
-
2013
- 2013-04-05 CL CL2013000934A patent/CL2013000934A1/es unknown
-
2016
- 2016-11-21 IL IL249101A patent/IL249101B/en active IP Right Grant
-
2017
- 2017-07-03 CY CY20171100703T patent/CY1119039T1/el unknown
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2009132681A5 (enExample) | ||
| RU2010122898A (ru) | Фунгицидная композиция и способ борьбы с вредными грибами | |
| AU2005289678B2 (en) | Fungicidal mixtures of thiophene derivative | |
| JP2007522187A5 (enExample) | ||
| DK2430921T3 (en) | SUBSTITUTED BENZEN FUNGICIDES | |
| JP2013536866A5 (enExample) | ||
| JP2014516064A5 (enExample) | ||
| CA2799788C (en) | Synergistic fungicidal active compound combinations | |
| EP2121660B1 (en) | Fungicidal amides | |
| JP2008501699A (ja) | アミジニルフェニル化合物の殺菌・殺カビ剤混合物 | |
| JP2015526408A5 (enExample) | ||
| RU2006132507A (ru) | Фунгицидная композиция, включающая производное пиридилэтилбензамида и соединение, способное ингибировать биосинтез эргостерола | |
| TWI513403B (zh) | 水性懸浮狀有害生物防除用組成物 | |
| SI2809157T1 (en) | Fungicidal pyrazole mixtures | |
| JP2016528201A5 (enExample) | ||
| RU2013114227A (ru) | Фунгицидные пиразолы и их смеси | |
| RU2013120094A (ru) | Фунгицидные композиции | |
| AR112211A1 (es) | Composiciones fungicidas | |
| JP2010138159A5 (enExample) | ||
| JP2011503006A (ja) | 殺菌性複素環アミン | |
| WO2010093595A1 (en) | Fungicidal 2-pyridones | |
| AR111343A1 (es) | Composiciones fungicidas | |
| JP2013501715A (ja) | 殺菌・殺カビ性ジフェニル−置換ピリダジン | |
| JP2008291023A (ja) | アミド化合物とその用途 | |
| US20090270407A1 (en) | Fungicidal isoxazolidines |