JPH0547553B2 - - Google Patents
Info
- Publication number
- JPH0547553B2 JPH0547553B2 JP63213486A JP21348688A JPH0547553B2 JP H0547553 B2 JPH0547553 B2 JP H0547553B2 JP 63213486 A JP63213486 A JP 63213486A JP 21348688 A JP21348688 A JP 21348688A JP H0547553 B2 JPH0547553 B2 JP H0547553B2
- Authority
- JP
- Japan
- Prior art keywords
- compound
- group
- trifluoromethyl
- hydroxypyrazole
- alkyl group
- 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.)
- Expired - Lifetime
Links
- XBYRMPXUBGMOJC-UHFFFAOYSA-N 1,2-dihydropyrazol-3-one Chemical class OC=1C=CNN=1 XBYRMPXUBGMOJC-UHFFFAOYSA-N 0.000 claims description 16
- 125000000217 alkyl group Chemical group 0.000 claims description 12
- 229910052739 hydrogen Inorganic materials 0.000 claims description 9
- 239000001257 hydrogen Substances 0.000 claims description 9
- 241000607479 Yersinia pestis Species 0.000 claims description 7
- 239000004480 active ingredient Substances 0.000 claims description 6
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 5
- 125000005843 halogen group Chemical group 0.000 claims description 5
- 239000003795 chemical substances by application Substances 0.000 claims description 4
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 3
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 3
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 3
- 125000003545 alkoxy group Chemical group 0.000 claims description 3
- 125000004414 alkyl thio group Chemical group 0.000 claims description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 3
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 3
- 229910052794 bromium Inorganic materials 0.000 claims description 3
- 125000004432 carbon atom Chemical group C* 0.000 claims description 3
- 239000000460 chlorine Substances 0.000 claims description 3
- 229910052801 chlorine Inorganic materials 0.000 claims description 3
- 150000002431 hydrogen Chemical class 0.000 claims description 3
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 claims description 3
- 229910052760 oxygen Inorganic materials 0.000 claims description 3
- 239000001301 oxygen Substances 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
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 3
- 230000001766 physiological effect Effects 0.000 claims description 3
- 229910052717 sulfur Chemical group 0.000 claims description 3
- 239000011593 sulfur Chemical group 0.000 claims description 3
- 150000001875 compounds Chemical class 0.000 description 78
- 238000012360 testing method Methods 0.000 description 39
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 33
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 30
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 30
- 238000004519 manufacturing process Methods 0.000 description 24
- 230000000749 insecticidal effect Effects 0.000 description 22
- -1 5-hydroxypyrazole compound Chemical class 0.000 description 17
- 238000000034 method Methods 0.000 description 16
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 16
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 15
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 12
- 238000006243 chemical reaction Methods 0.000 description 12
- 239000000203 mixture Substances 0.000 description 12
- 239000003814 drug Substances 0.000 description 10
- 229940079593 drug Drugs 0.000 description 10
- 239000002904 solvent Substances 0.000 description 10
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 9
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 9
- 239000000243 solution Substances 0.000 description 9
- 241000238631 Hexapoda Species 0.000 description 8
- 229910019142 PO4 Inorganic materials 0.000 description 8
- 239000010452 phosphate Substances 0.000 description 8
- 229910000027 potassium carbonate Inorganic materials 0.000 description 8
- 239000007788 liquid Substances 0.000 description 7
- 239000000575 pesticide Substances 0.000 description 7
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 6
- WQRHIGNAKDJJKN-UHFFFAOYSA-N 2-methyl-5-(trifluoromethyl)-1h-pyrazol-3-one Chemical compound CN1NC(C(F)(F)F)=CC1=O WQRHIGNAKDJJKN-UHFFFAOYSA-N 0.000 description 6
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 6
- 239000012046 mixed solvent Substances 0.000 description 6
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 6
- 239000002728 pyrethroid Substances 0.000 description 6
- 238000010898 silica gel chromatography Methods 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- 241000238876 Acari Species 0.000 description 5
- 235000010149 Brassica rapa subsp chinensis Nutrition 0.000 description 5
- 235000000536 Brassica rapa subsp pekinensis Nutrition 0.000 description 5
- 241000499436 Brassica rapa subsp. pekinensis Species 0.000 description 5
- 239000012872 agrochemical composition Substances 0.000 description 5
- 239000000843 powder Substances 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
- HEDRZPFGACZZDS-MICDWDOJSA-N Trichloro(2H)methane Chemical compound [2H]C(Cl)(Cl)Cl HEDRZPFGACZZDS-MICDWDOJSA-N 0.000 description 4
- 150000001298 alcohols Chemical class 0.000 description 4
- 239000007795 chemical reaction product Substances 0.000 description 4
- KMJJJTCKNZYTEY-UHFFFAOYSA-N chloro-diethoxy-sulfanylidene-$l^{5}-phosphane Chemical compound CCOP(Cl)(=S)OCC KMJJJTCKNZYTEY-UHFFFAOYSA-N 0.000 description 4
- LGTLXDJOAJDFLR-UHFFFAOYSA-N diethyl chlorophosphate Chemical compound CCOP(Cl)(=O)OCC LGTLXDJOAJDFLR-UHFFFAOYSA-N 0.000 description 4
- 239000000839 emulsion Substances 0.000 description 4
- 239000008187 granular material Substances 0.000 description 4
- 239000002917 insecticide Substances 0.000 description 4
- PSHKMPUSSFXUIA-UHFFFAOYSA-N n,n-dimethylpyridin-2-amine Chemical compound CN(C)C1=CC=CC=N1 PSHKMPUSSFXUIA-UHFFFAOYSA-N 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- 125000001424 substituent group Chemical group 0.000 description 4
- RYYWUUFWQRZTIU-UHFFFAOYSA-K thiophosphate Chemical compound [O-]P([O-])([O-])=S RYYWUUFWQRZTIU-UHFFFAOYSA-K 0.000 description 4
- 239000004563 wettable powder Substances 0.000 description 4
- PSQCMVQGPMFFCX-UHFFFAOYSA-N 2-phenyl-5-(trifluoromethyl)-1h-pyrazol-3-one Chemical compound N1C(C(F)(F)F)=CC(=O)N1C1=CC=CC=C1 PSQCMVQGPMFFCX-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- GETXLGYLYDWIBI-UHFFFAOYSA-N CN1N=C(C(F)(F)F)C(Cl)=C1O Chemical compound CN1N=C(C(F)(F)F)C(Cl)=C1O GETXLGYLYDWIBI-UHFFFAOYSA-N 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- 241001556089 Nilaparvata lugens Species 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 239000000440 bentonite Substances 0.000 description 3
- 229910000278 bentonite Inorganic materials 0.000 description 3
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 3
- 239000000969 carrier Substances 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 238000000746 purification Methods 0.000 description 3
- 238000000926 separation method Methods 0.000 description 3
- 238000001228 spectrum Methods 0.000 description 3
- 150000003580 thiophosphoric acid esters Chemical class 0.000 description 3
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 2
- 238000005160 1H NMR spectroscopy Methods 0.000 description 2
- RJAVFPJSNYFSKY-UHFFFAOYSA-N 2-(4-chlorophenyl)-5-(trifluoromethyl)-1h-pyrazol-3-one Chemical compound N1C(C(F)(F)F)=CC(=O)N1C1=CC=C(Cl)C=C1 RJAVFPJSNYFSKY-UHFFFAOYSA-N 0.000 description 2
- PYXNITNKYBLBMW-UHFFFAOYSA-N 5-(trifluoromethyl)-1h-pyrazole Chemical compound FC(F)(F)C1=CC=NN1 PYXNITNKYBLBMW-UHFFFAOYSA-N 0.000 description 2
- 239000005995 Aluminium silicate Substances 0.000 description 2
- 240000007124 Brassica oleracea Species 0.000 description 2
- 235000003899 Brassica oleracea var acephala Nutrition 0.000 description 2
- 235000011301 Brassica oleracea var capitata Nutrition 0.000 description 2
- 235000001169 Brassica oleracea var oleracea Nutrition 0.000 description 2
- 239000005892 Deltamethrin Substances 0.000 description 2
- 241000255925 Diptera Species 0.000 description 2
- 241000196324 Embryophyta Species 0.000 description 2
- 241001466042 Fulgoromorpha Species 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- 244000061176 Nicotiana tabacum Species 0.000 description 2
- 235000002637 Nicotiana tabacum Nutrition 0.000 description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
- GIJYCEVUYXZYQX-UHFFFAOYSA-N OC1=C(Cl)C(C(F)(F)F)=NN1C1=CC=CC=C1 Chemical compound OC1=C(Cl)C(C(F)(F)F)=NN1C1=CC=CC=C1 GIJYCEVUYXZYQX-UHFFFAOYSA-N 0.000 description 2
- OYPOJLQBKIQKOC-UHFFFAOYSA-N OC1=CC(C(F)(F)F)=NN1C1=CC=C(Cl)C=C1Cl Chemical compound OC1=CC(C(F)(F)F)=NN1C1=CC=C(Cl)C=C1Cl OYPOJLQBKIQKOC-UHFFFAOYSA-N 0.000 description 2
- 240000007594 Oryza sativa Species 0.000 description 2
- 235000007164 Oryza sativa Nutrition 0.000 description 2
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
- 239000002202 Polyethylene glycol Substances 0.000 description 2
- 241000133716 Riptortus clavatus Species 0.000 description 2
- 241000985245 Spodoptera litura Species 0.000 description 2
- NGFFLHMFSINFGB-UHFFFAOYSA-N [chloro(methoxy)phosphoryl]oxymethane Chemical compound COP(Cl)(=O)OC NGFFLHMFSINFGB-UHFFFAOYSA-N 0.000 description 2
- 230000000895 acaricidal effect Effects 0.000 description 2
- 239000003905 agrochemical Substances 0.000 description 2
- 150000001340 alkali metals Chemical class 0.000 description 2
- 235000012211 aluminium silicate Nutrition 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- 239000003153 chemical reaction reagent Substances 0.000 description 2
- 239000004927 clay Substances 0.000 description 2
- 229960002483 decamethrin Drugs 0.000 description 2
- OWZREIFADZCYQD-NSHGMRRFSA-N deltamethrin Chemical compound CC1(C)[C@@H](C=C(Br)Br)[C@H]1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 OWZREIFADZCYQD-NSHGMRRFSA-N 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- YDEXUEFDPVHGHE-GGMCWBHBSA-L disodium;(2r)-3-(2-hydroxy-3-methoxyphenyl)-2-[2-methoxy-4-(3-sulfonatopropyl)phenoxy]propane-1-sulfonate Chemical compound [Na+].[Na+].COC1=CC=CC(C[C@H](CS([O-])(=O)=O)OC=2C(=CC(CCCS([O-])(=O)=O)=CC=2)OC)=C1O YDEXUEFDPVHGHE-GGMCWBHBSA-L 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000005886 esterification reaction Methods 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 150000002170 ethers Chemical class 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 239000000706 filtrate Substances 0.000 description 2
- 229910052736 halogen Inorganic materials 0.000 description 2
- 230000002140 halogenating effect Effects 0.000 description 2
- 150000002367 halogens Chemical class 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 229920001223 polyethylene glycol Polymers 0.000 description 2
- 150000003217 pyrazoles Chemical class 0.000 description 2
- 235000009566 rice Nutrition 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 2
- 239000008096 xylene Substances 0.000 description 2
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 1
- 239000004342 Benzoyl peroxide Substances 0.000 description 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical class OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 1
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 1
- UGVAQFVQIHNCJV-UHFFFAOYSA-N CN1N=C(C(F)(F)F)C=C1O Chemical compound CN1N=C(C(F)(F)F)C=C1O UGVAQFVQIHNCJV-UHFFFAOYSA-N 0.000 description 1
- 241001498622 Cixius wagneri Species 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- 241000256059 Culex pipiens Species 0.000 description 1
- 241000144210 Culex pipiens pallens Species 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- 244000068988 Glycine max Species 0.000 description 1
- 235000010469 Glycine max Nutrition 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- 241000721621 Myzus persicae Species 0.000 description 1
- 238000005481 NMR spectroscopy Methods 0.000 description 1
- 244000046052 Phaseolus vulgaris Species 0.000 description 1
- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 1
- 241000500439 Plutella Species 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- WTKZEGDFNFYCGP-UHFFFAOYSA-N Pyrazole Chemical compound C=1C=NNC=1 WTKZEGDFNFYCGP-UHFFFAOYSA-N 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- 241001414987 Strepsiptera Species 0.000 description 1
- 240000004460 Tanacetum coccineum Species 0.000 description 1
- ROVGZAWFACYCSP-MQBLHHJJSA-N [2-methyl-4-oxo-3-[(2z)-penta-2,4-dienyl]cyclopent-2-en-1-yl] (1r,3r)-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropane-1-carboxylate Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OC1C(C)=C(C\C=C/C=C)C(=O)C1 ROVGZAWFACYCSP-MQBLHHJJSA-N 0.000 description 1
- 239000000642 acaricide Substances 0.000 description 1
- 238000007605 air drying Methods 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 229910000272 alkali metal oxide Inorganic materials 0.000 description 1
- 229910001860 alkaline earth metal hydroxide Inorganic materials 0.000 description 1
- 229940045714 alkyl sulfonate alkylating agent Drugs 0.000 description 1
- 150000008052 alkyl sulfonates Chemical class 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- 230000004071 biological effect Effects 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 239000003093 cationic surfactant Substances 0.000 description 1
- 239000007805 chemical reaction reactant Substances 0.000 description 1
- XFBJRFNXPUCPKU-UHFFFAOYSA-N chloro-dimethoxy-sulfanylidene-$l^{5}-phosphane Chemical compound COP(Cl)(=S)OC XFBJRFNXPUCPKU-UHFFFAOYSA-N 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 238000004440 column chromatography Methods 0.000 description 1
- 239000012043 crude product Substances 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000003337 fertilizer Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 238000004817 gas chromatography Methods 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 238000005469 granulation Methods 0.000 description 1
- 230000003179 granulation Effects 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 239000004009 herbicide Substances 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
- WJRBRSLFGCUECM-UHFFFAOYSA-N hydantoin Chemical compound O=C1CNC(=O)N1 WJRBRSLFGCUECM-UHFFFAOYSA-N 0.000 description 1
- 229940091173 hydantoin Drugs 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 239000003350 kerosene Substances 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 239000003375 plant hormone Substances 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 229940015367 pyrethrum Drugs 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000003892 spreading Methods 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- YBBRCQOCSYXUOC-UHFFFAOYSA-N sulfuryl dichloride Chemical compound ClS(Cl)(=O)=O YBBRCQOCSYXUOC-UHFFFAOYSA-N 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 238000001308 synthesis method Methods 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 239000010455 vermiculite Substances 0.000 description 1
- 229910052902 vermiculite Inorganic materials 0.000 description 1
- 235000019354 vermiculite Nutrition 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D231/18—One oxygen or sulfur atom
- C07D231/20—One oxygen atom attached in position 3 or 5
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D231/18—One oxygen or sulfur atom
- C07D231/20—One oxygen atom attached in position 3 or 5
- C07D231/22—One oxygen atom attached in position 3 or 5 with aryl radicals attached to ring nitrogen atoms
-
- 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
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/10—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds
- A01N57/16—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds containing heterocyclic radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/645—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having two nitrogen atoms as the only ring hetero atoms
- C07F9/6503—Five-membered rings
- C07F9/65031—Five-membered rings having the nitrogen atoms in the positions 1 and 2
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Dentistry (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Biochemistry (AREA)
- Molecular Biology (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| KR1019880003318A KR900003088B1 (ko) | 1988-03-26 | 1988-03-26 | 5-하이드록시피라졸 유도체 |
| KR3318 | 1988-03-26 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH01249789A JPH01249789A (ja) | 1989-10-05 |
| JPH0547553B2 true JPH0547553B2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1993-07-19 |
Family
ID=19273149
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP63213486A Granted JPH01249789A (ja) | 1988-03-26 | 1988-08-26 | ５−ヒドロキシピラゾール誘導体 |
Country Status (3)
Families Citing this family (78)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5959087A (en) * | 1989-08-07 | 1999-09-28 | Peptide Technology, Ltd. | Tumour necrosis factor binding ligands |
| DE4315384A1 (de) * | 1992-09-03 | 1994-03-10 | Bayer Ag | Phosphoryloxypyrazolderivate |
| CA2610085A1 (en) * | 2005-06-03 | 2006-12-07 | Basf Aktiengesellschaft | Pesticidal mixture |
| CN101506150B (zh) | 2006-06-22 | 2013-08-28 | 巴斯夫欧洲公司 | 丙二腈化合物 |
| MX2009002219A (es) | 2006-09-14 | 2009-04-17 | Basf Se | Composicion pesticida. |
| EA018341B1 (ru) | 2006-11-10 | 2013-07-30 | Басф Се | Новая кристаллическая модификация фипронила и ее применение |
| UA110598C2 (uk) | 2006-11-10 | 2016-01-25 | Басф Се | Спосіб одержання кристалічної модифікації фіпронілу |
| ATE513470T1 (de) | 2006-11-10 | 2011-07-15 | Basf Se | Kristalline fipronil-modifikation |
| MX2009004323A (es) | 2006-11-10 | 2009-05-05 | Basf Se | Nueva modificacion cristalina. |
| ES2346263T3 (es) * | 2006-11-30 | 2010-10-13 | Basf Se | Formulaciones agroquimicas que comprenden copolimeros de n-vinilamida. |
| CN101541168B (zh) * | 2006-11-30 | 2013-05-15 | 巴斯夫欧洲公司 | 包含基于二异氰酸酯的共聚物的农业化学配制剂 |
| CN101562969B (zh) * | 2006-11-30 | 2013-12-25 | 巴斯夫欧洲公司 | 包含1-乙烯基-2-吡咯烷酮共聚物的农业化学配制剂 |
| WO2008071714A1 (en) | 2006-12-15 | 2008-06-19 | Rohm And Haas Company | Mixtures comprising 1-methylcyclopropene |
| CA2673992A1 (en) * | 2007-01-19 | 2008-07-24 | Basf Se | Fungicidal mixtures of 1-methylpyrazol-4-ylcarboxanilides and azolopyrimidinylamines |
| US8119568B2 (en) | 2007-01-26 | 2012-02-21 | Basf Se | 3-amino-1,2-benzisothiazole compounds for combating animal pest II |
| CA2674533A1 (en) * | 2007-01-30 | 2008-08-07 | Basf Se | Pesticidal mixtures based on azolopyrimidinylamines derivatives and insecticides |
| EP1952690A3 (en) | 2007-01-31 | 2009-04-22 | Basf Se | Pesticidal mixtures based on triazolopyrimidines and insecticides |
| CN101605461A (zh) | 2007-02-06 | 2009-12-16 | 巴斯夫欧洲公司 | 农药混合物 |
| EP3199026A1 (en) | 2007-04-12 | 2017-08-02 | Basf Se | Pesticidal mixtures comprising cyanosulfoximine compounds |
| US20100093715A1 (en) | 2007-04-23 | 2010-04-15 | Basf Se | Plant productivity enhancement by combining chemical agents with transgenic modifications |
| PL2180783T3 (pl) | 2007-08-16 | 2017-08-31 | Basf Se | Kompozycje i sposoby d o zaprawiania nasion |
| NZ599174A (en) * | 2007-09-20 | 2012-08-31 | Basf Se | Combinations comprising a fungicidal strain and an azolopyrimidin-7-ylamine |
| WO2009080464A2 (en) * | 2007-12-21 | 2009-07-02 | Basf Se | Process for the production of insecticide-modified bead material composed of expandable polystyrene and insecticide-modified moldings obtainable therefrom |
| KR20100105614A (ko) * | 2007-12-21 | 2010-09-29 | 바스프 에스이 | 발포성 폴리스티렌으로 이루어진 살충제-함유 입자 및 이들로부터 수득할 수 있는 살충제-함유 성형물 |
| US20100311582A1 (en) | 2008-01-25 | 2010-12-09 | Syngenta Crop Protection, Inc. | Chemical compounds |
| MX2011004119A (es) * | 2008-10-22 | 2011-05-04 | Basf Se | Metodo para producir piezas moldeadas de xps provistas con insecticida. |
| JP2012513379A (ja) | 2008-12-23 | 2012-06-14 | ビーエーエスエフ ソシエタス・ヨーロピア | 有害生物に対する保護活性を付与するための非生物材料の含浸方法および含浸用水性製剤 |
| AR075166A1 (es) | 2009-01-27 | 2011-03-16 | Basf Se | Metodo para desinfectar semillas |
| WO2010089244A1 (en) | 2009-02-03 | 2010-08-12 | Basf Se | Method for dressing seeds |
| AU2010220293B2 (en) | 2009-03-04 | 2014-09-11 | Basf Se | 3-arylquinazolin-4-one compounds for combating invertebrate pests |
| WO2010112545A1 (en) | 2009-04-01 | 2010-10-07 | Basf Se | Isoxazoline compounds for combating invertebrate pests |
| TW201114366A (en) * | 2009-04-28 | 2011-05-01 | Basf Corp | Pesticide compositions and applicators |
| EA022081B1 (ru) | 2009-04-28 | 2015-10-30 | Басф Корпорейшн | Пенообразующие пестицидные композиции |
| WO2011003796A1 (en) | 2009-07-06 | 2011-01-13 | Basf Se | Pyridazine compounds for controlling invertebrate pests |
| JP2013500246A (ja) | 2009-07-24 | 2013-01-07 | ビーエーエスエフ ソシエタス・ヨーロピア | 無脊椎動物系害虫防除用ピリジン誘導体化合物 |
| JP5834006B2 (ja) | 2009-07-30 | 2015-12-16 | メリアル リミテッド | 殺虫性４−アミノ−チエノ［２，３−ｄ］−ピリミジン化合物及びその使用方法 |
| KR20120061931A (ko) | 2009-08-28 | 2012-06-13 | 바스프 코포레이션 | 발포성 살충제 조성물 및 적용 방법 |
| JP2013505909A (ja) | 2009-09-24 | 2013-02-21 | ビーエーエスエフ ソシエタス・ヨーロピア | 無脊椎動物害虫を駆除するためのアミノキナゾリン化合物 |
| WO2011057942A1 (en) | 2009-11-12 | 2011-05-19 | Basf Se | Insecticidal methods using pyridine compounds |
| WO2011061110A1 (en) | 2009-11-17 | 2011-05-26 | Basf Se | Fluorinated oxa or thia heteroarylalkylsulfide derivatives for combating invertebrate pests |
| WO2011064188A1 (en) | 2009-11-27 | 2011-06-03 | Basf Se | Insecticidal methods using nitrogen-containing heteroaromatic compounds |
| US8846569B2 (en) | 2009-12-04 | 2014-09-30 | Merial Limited | Pesticidal bis-organosulfur compounds |
| WO2011069955A1 (en) | 2009-12-07 | 2011-06-16 | Basf Se | Sulfonimidamide compounds for combating animal pests |
| US20120291159A1 (en) | 2009-12-18 | 2012-11-15 | Basf Se | Azoline Compounds for Combating Invertebrate Pests |
| BR112012019103A2 (pt) | 2010-02-01 | 2015-10-20 | Basf Se | compostos de isoxazolina cetônica, composto cetônico, composição agrícola, composição veterinária, uso de um composto, método e material de propagação de planta |
| CN102834391A (zh) | 2010-03-23 | 2012-12-19 | 巴斯夫欧洲公司 | 防治无脊椎动物害虫的哒嗪化合物 |
| WO2011117806A2 (en) | 2010-03-23 | 2011-09-29 | Basf Se | Pyridazine compounds for controlling invertebrate pests |
| ES2589792T3 (es) | 2010-03-23 | 2016-11-16 | Basf Se | Compuestos de piridazina para el control de plagas de invertebrados |
| US20130131091A1 (en) | 2010-05-24 | 2013-05-23 | Kimihiko Goto | Harmful organism control agent |
| ES2527246T3 (es) | 2010-05-28 | 2015-01-21 | Basf Se | Mezclas plaguicidas |
| WO2012007426A1 (en) | 2010-07-13 | 2012-01-19 | Basf Se | Azoline substituted isoxazoline benzamide compounds for combating animal pests |
| EA201201673A1 (ru) | 2010-07-22 | 2013-06-28 | Басф Се | Новые гетарил(тио)карбоксамидные соединения для борьбы с беспозвоночными вредителями |
| US8609700B2 (en) | 2010-09-13 | 2013-12-17 | Basf Se | Pyridine compounds for controlling invertebrate pests I |
| US20130203821A1 (en) | 2010-09-13 | 2013-08-08 | Basf Se | Pyridine Compounds for Controlling Invertebrate Pests II |
| EP2615917A2 (en) | 2010-09-13 | 2013-07-24 | Basf Se | Pyridine compounds for controlling invertebrate pests iii |
| US20130184320A1 (en) | 2010-10-01 | 2013-07-18 | Basf Se | Imine Compounds |
| JP2013540116A (ja) | 2010-10-01 | 2013-10-31 | ビーエーエスエフ ソシエタス・ヨーロピア | 殺有害生物剤としてのイミン置換−２，４−ジアリール−ピロリン誘導体 |
| BR112013013623A2 (pt) | 2010-12-10 | 2016-07-12 | Basf Se | métodos para controlar pragas invertebradas e para proteger material de propagagação de planta e/ou as plantas, material de propagação de planta, uso de um composto da fórmula i e composto de pirazol da fórmula i |
| KR20130132942A (ko) | 2010-12-20 | 2013-12-05 | 바스프 에스이 | 피라졸 화합물을 포함하는 살충 활성 혼합물 |
| WO2012085081A1 (en) | 2010-12-22 | 2012-06-28 | Basf Se | Sulfoximinamide compounds for combating invertebrate pests ii |
| US9179680B2 (en) | 2011-04-06 | 2015-11-10 | Basf Se | Substituted pyrimidinium compounds for combating animal pests |
| MX354349B (es) | 2011-04-21 | 2018-02-27 | Basf Se | Novedosos compuestos de pirazol pesticidas. |
| JP2014522876A (ja) | 2011-08-12 | 2014-09-08 | ビーエーエスエフ ソシエタス・ヨーロピア | Ｎ−チオ−アントラニルアミド化合物、及び殺有害生物剤としてのそれらの使用 |
| US9044016B2 (en) | 2011-08-12 | 2015-06-02 | Basf Se | N-thio-anthranilamide compounds and their use as pesticides |
| WO2013024004A1 (en) | 2011-08-12 | 2013-02-21 | Basf Se | N-thio-anthranilamide compounds and their use as pesticides |
| JP2014522873A (ja) | 2011-08-12 | 2014-09-08 | ビーエーエスエフ ソシエタス・ヨーロピア | アントラニルアミド化合物および殺虫剤としてのその使用 |
| MX2014001510A (es) | 2011-08-12 | 2014-05-12 | Basf Se | Compuestos de antranilamida y sus usos como plaguicidas. |
| US20140243195A1 (en) | 2011-08-12 | 2014-08-28 | Basf Se | N-Thio-anthranilamide compounds and their use as pesticides |
| CN103889956A (zh) | 2011-08-18 | 2014-06-25 | 巴斯夫欧洲公司 | 用于防治无脊椎动物害虫的氨基甲酰基甲氧基-和氨基甲酰基甲硫基-及氨基甲酰基甲基氨基苯甲酰胺 |
| BR112014003649A2 (pt) | 2011-08-18 | 2017-03-21 | Basf Se | composto da fórmula (i), método, composição agrícola ou veterinária, semente e uso de um composto definido |
| CN103889960A (zh) | 2011-08-18 | 2014-06-25 | 巴斯夫欧洲公司 | 用于防治无脊椎动物害虫的氨基甲酰基甲氧基-和氨基甲酰基甲硫基-及氨基甲酰基甲基氨基苯甲酰胺 |
| EP2750506A2 (en) | 2011-09-02 | 2014-07-09 | Basf Se | Use of pesticidal active 3-arylquinazolin-4-one derivatives in soil application methods |
| US9487523B2 (en) | 2012-03-14 | 2016-11-08 | Merck Sharp & Dohme Corp. | Process for making CGRP receptor antagonists |
| EP2684879A1 (en) | 2012-07-09 | 2014-01-15 | Basf Se | Substituted mesoionic compounds for combating animal pests |
| US20150230470A1 (en) | 2012-09-21 | 2015-08-20 | Basf Se | Pyrethroid Insecticide For Protecting Plants And Seed |
| CN103651553B (zh) * | 2013-11-21 | 2014-12-17 | 海南正业中农高科股份有限公司 | 含有吡氟硫磷的农药组合物 |
| AR100304A1 (es) | 2014-02-05 | 2016-09-28 | Basf Corp | Formulación de recubrimiento de semillas |
| UY37137A (es) | 2016-02-24 | 2017-09-29 | Merial Inc | Compuestos antiparasitarios de isoxazolina, formulaciones inyectables de acción prolongada que los comprenden, métodos y usos de los mismos |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4466962A (en) * | 1983-02-28 | 1984-08-21 | Chevron Research Company | Insecticidal 1-alkyl-5-substituted-4-chloropyrazole-3-yl-(thio) phosphates and (thio) phosphonates |
-
1988
- 1988-03-26 KR KR1019880003318A patent/KR900003088B1/ko not_active Expired
- 1988-08-15 US US07/233,098 patent/US4822779A/en not_active Expired - Lifetime
- 1988-08-26 JP JP63213486A patent/JPH01249789A/ja active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| KR890014492A (ko) | 1989-10-24 |
| JPH01249789A (ja) | 1989-10-05 |
| KR900003088B1 (ko) | 1990-05-07 |
| US4822779A (en) | 1989-04-18 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JPH0547553B2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | ||
| EP0641316A1 (en) | INSECTICIDE DERIVATIVES OF PHENYLHYDRAZINE. | |
| KR0140208B1 (ko) | 살충, 살비활성의 피리다지논 | |
| JP3968012B2 (ja) | 除草活性を持った５−ベンジルオキシメチル−１，２−イソオキサゾリン誘導体 | |
| JP2613651B2 (ja) | オキサー又はチアゾリン化合物及びこれを含有する殺虫、殺ダニ剤 | |
| JP3279818B2 (ja) | 殺虫・殺ダニ剤 | |
| KR100349484B1 (ko) | 식물병해방제제 | |
| JPS6348862B2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | ||
| JP3870515B2 (ja) | ５，６−ジヒドロ−（４ｈ）−１，３−チアジン誘導体、その製法及び農園芸用の有害生物防除剤 | |
| US4123526A (en) | Thionophosphate insecticide activators | |
| US4209512A (en) | Mono- and di-thiophosphate esters containing an isoxazolinone ring and compositions and methods containing the same | |
| KR950009521B1 (ko) | 살충제로 유용한 피레스로이드 유도체 | |
| EP0395422B1 (en) | Cyclohexane derivatives, its salts and uses as insecticides | |
| KR900002057B1 (ko) | 생리활성을 갖는 신규한 5-하이드록시피라졸유도체 | |
| JP4512928B2 (ja) | Ｎ−チアジアゾリルシクロアルカンカルボン酸アミド類およびこれを有効成分とする殺虫、殺ダニ剤 | |
| KR900002055B1 (ko) | 생리활성을 가진 피라졸 유도체 및 그 제조방법 | |
| KR940007420B1 (ko) | 피라졸 인산에스테르 유도체 | |
| KR100256548B1 (ko) | 신규한 불소화 프로페닐옥시아세트아미드 및 그의 제조방법 | |
| JPH03197467A (ja) | ピリミジノン誘導体その製法及びそれを有効成分とする殺虫・殺ダニ剤 | |
| JPH05286970A (ja) | ２−アシルアミノ−２−チアゾリン化合物、その製法及び有害生物防除剤 | |
| US3904639A (en) | Thiazolotriazolyphosphonothioates | |
| US4024252A (en) | 2-(5-Ethyl-6-bromothiazolo[3,2-b]-5-triazolyl)thiophosphonate esters, compositions and method of use | |
| US4137065A (en) | Amido phosphorothiolate pesticide | |
| KR100285539B1 (ko) | 플루오로알케닐기가 치환된 신규의 옥시아세트아닐리드 및 그의제조방법 | |
| JPH0665239A (ja) | ２−アシルアミノ−２−チアゾリン化合物、その製法及び有害生物防除剤 |