RU2599725C2 - Производное соединение сложного эфира 2-аминоникотиновой кислоты и бактерицид, содержащий то же самое в качестве активного ингредиента - Google Patents
Производное соединение сложного эфира 2-аминоникотиновой кислоты и бактерицид, содержащий то же самое в качестве активного ингредиента Download PDFInfo
- Publication number
- RU2599725C2 RU2599725C2 RU2015103515/04A RU2015103515A RU2599725C2 RU 2599725 C2 RU2599725 C2 RU 2599725C2 RU 2015103515/04 A RU2015103515/04 A RU 2015103515/04A RU 2015103515 A RU2015103515 A RU 2015103515A RU 2599725 C2 RU2599725 C2 RU 2599725C2
- Authority
- RU
- Russia
- Prior art keywords
- group
- compound
- patent document
- tree
- aminonicotinic acid
- Prior art date
Links
- 230000000844 anti-bacterial effect Effects 0.000 title claims abstract description 27
- -1 Ester derivative of 2-aminonicotinic acid Chemical class 0.000 title claims description 116
- 239000003899 bactericide agent Substances 0.000 title claims description 17
- 239000004480 active ingredient Substances 0.000 title claims description 15
- 150000001875 compounds Chemical class 0.000 claims abstract description 99
- KPIVDNYJNOPGBE-UHFFFAOYSA-N 2-aminonicotinic acid Chemical compound NC1=NC=CC=C1C(O)=O KPIVDNYJNOPGBE-UHFFFAOYSA-N 0.000 claims abstract description 8
- 150000002148 esters Chemical class 0.000 claims abstract description 4
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 12
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 11
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 5
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 claims description 3
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims description 3
- 125000005843 halogen group Chemical group 0.000 claims description 3
- 125000001434 methanylylidene group Chemical group [H]C#[*] 0.000 claims description 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 2
- 229910052757 nitrogen Inorganic materials 0.000 claims description 2
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 2
- 125000004644 alkyl sulfinyl group Chemical group 0.000 claims 1
- 230000000694 effects Effects 0.000 abstract description 7
- 239000000126 substance Substances 0.000 abstract description 7
- 239000000203 mixture Substances 0.000 description 18
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical group C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 17
- 125000003277 amino group Chemical group 0.000 description 14
- 238000006243 chemical reaction Methods 0.000 description 14
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- 238000003898 horticulture Methods 0.000 description 8
- 230000004526 pharmaceutical effect Effects 0.000 description 8
- 239000002904 solvent Substances 0.000 description 8
- 240000008067 Cucumis sativus Species 0.000 description 7
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 7
- 238000004519 manufacturing process Methods 0.000 description 7
- 239000004563 wettable powder Substances 0.000 description 7
- 238000005160 1H NMR spectroscopy Methods 0.000 description 6
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 239000013543 active substance Substances 0.000 description 6
- 239000004495 emulsifiable concentrate Substances 0.000 description 6
- 230000002363 herbicidal effect Effects 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- 241000894006 Bacteria Species 0.000 description 5
- 235000010799 Cucumis sativus var sativus Nutrition 0.000 description 5
- 241000588702 Pectobacterium carotovorum subsp. carotovorum Species 0.000 description 5
- 241000589771 Ralstonia solanacearum Species 0.000 description 5
- 244000052616 bacterial pathogen Species 0.000 description 5
- 239000003795 chemical substances by application Substances 0.000 description 5
- 239000002002 slurry Substances 0.000 description 5
- 239000004546 suspension concentrate Substances 0.000 description 5
- 241000123650 Botrytis cinerea Species 0.000 description 4
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 4
- 240000007594 Oryza sativa Species 0.000 description 4
- 150000001298 alcohols Chemical class 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 0 C*(*)(Cc1ccccc1)C(C(C(C)=*)=CC=*)=O Chemical compound C*(*)(Cc1ccccc1)C(C(C(C)=*)=CC=*)=O 0.000 description 3
- 241000548268 Citrus deliciosa Species 0.000 description 3
- 241000219112 Cucumis Species 0.000 description 3
- 235000015510 Cucumis melo subsp melo Nutrition 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- 240000005979 Hordeum vulgare Species 0.000 description 3
- 235000007340 Hordeum vulgare Nutrition 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 3
- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 3
- 244000046052 Phaseolus vulgaris Species 0.000 description 3
- 235000010582 Pisum sativum Nutrition 0.000 description 3
- 240000004713 Pisum sativum Species 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 235000002595 Solanum tuberosum Nutrition 0.000 description 3
- 244000061456 Solanum tuberosum Species 0.000 description 3
- 244000269722 Thea sinensis Species 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 244000098338 Triticum aestivum Species 0.000 description 3
- 241000589649 Xanthomonas campestris pv. campestris Species 0.000 description 3
- 239000002671 adjuvant Substances 0.000 description 3
- 239000003905 agrochemical Substances 0.000 description 3
- 239000003945 anionic surfactant Substances 0.000 description 3
- 230000009969 flowable effect Effects 0.000 description 3
- 239000008187 granular material Substances 0.000 description 3
- 239000004009 herbicide Substances 0.000 description 3
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 3
- 230000000749 insecticidal effect Effects 0.000 description 3
- 239000002917 insecticide Substances 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 239000002736 nonionic surfactant Substances 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- 235000019198 oils Nutrition 0.000 description 3
- 230000000361 pesticidal effect Effects 0.000 description 3
- 235000012015 potatoes Nutrition 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 238000003892 spreading Methods 0.000 description 3
- 239000004094 surface-active agent Substances 0.000 description 3
- 235000013311 vegetables Nutrition 0.000 description 3
- 239000008096 xylene Substances 0.000 description 3
- 125000004768 (C1-C4) alkylsulfinyl group Chemical group 0.000 description 2
- LMDZBCPBFSXMTL-UHFFFAOYSA-N 1-Ethyl-3-(3-dimethylaminopropyl)carbodiimide Substances CCN=C=NCCCN(C)C LMDZBCPBFSXMTL-UHFFFAOYSA-N 0.000 description 2
- QPUYECUOLPXSFR-UHFFFAOYSA-N 1-methylnaphthalene Chemical compound C1=CC=C2C(C)=CC=CC2=C1 QPUYECUOLPXSFR-UHFFFAOYSA-N 0.000 description 2
- GQHTUMJGOHRCHB-UHFFFAOYSA-N 2,3,4,6,7,8,9,10-octahydropyrimido[1,2-a]azepine Chemical compound C1CCCCN2CCCN=C21 GQHTUMJGOHRCHB-UHFFFAOYSA-N 0.000 description 2
- FPQQSJJWHUJYPU-UHFFFAOYSA-N 3-(dimethylamino)propyliminomethylidene-ethylazanium;chloride Chemical compound Cl.CCN=C=NCCCN(C)C FPQQSJJWHUJYPU-UHFFFAOYSA-N 0.000 description 2
- VHYFNPMBLIVWCW-UHFFFAOYSA-N 4-Dimethylaminopyridine Chemical compound CN(C)C1=CC=NC=C1 VHYFNPMBLIVWCW-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- 241000589155 Agrobacterium tumefaciens Species 0.000 description 2
- 235000005254 Allium ampeloprasum Nutrition 0.000 description 2
- 240000006108 Allium ampeloprasum Species 0.000 description 2
- 241000213004 Alternaria solani Species 0.000 description 2
- 244000144730 Amygdalus persica Species 0.000 description 2
- 241000219310 Beta vulgaris subsp. vulgaris Species 0.000 description 2
- 241000167854 Bourreria succulenta Species 0.000 description 2
- 240000002791 Brassica napus Species 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- 235000007516 Chrysanthemum Nutrition 0.000 description 2
- 241001123536 Colletotrichum acutatum Species 0.000 description 2
- 229940126062 Compound A Drugs 0.000 description 2
- 244000000626 Daucus carota Species 0.000 description 2
- 235000002767 Daucus carota Nutrition 0.000 description 2
- QOSSAOTZNIDXMA-UHFFFAOYSA-N Dicylcohexylcarbodiimide Chemical compound C1CCCCC1N=C=NC1CCCCC1 QOSSAOTZNIDXMA-UHFFFAOYSA-N 0.000 description 2
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 2
- 235000011511 Diospyros Nutrition 0.000 description 2
- 244000236655 Diospyros kaki Species 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- 240000009088 Fragaria x ananassa Species 0.000 description 2
- 241001071795 Gentiana Species 0.000 description 2
- 235000010469 Glycine max Nutrition 0.000 description 2
- 241000896246 Golovinomyces cichoracearum Species 0.000 description 2
- 244000020551 Helianthus annuus Species 0.000 description 2
- 235000003222 Helianthus annuus Nutrition 0.000 description 2
- NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 description 2
- 235000007688 Lycopersicon esculentum Nutrition 0.000 description 2
- 241000218922 Magnoliophyta Species 0.000 description 2
- 235000011430 Malus pumila Nutrition 0.000 description 2
- 235000015103 Malus silvestris Nutrition 0.000 description 2
- 241001518731 Monilinia fructicola Species 0.000 description 2
- 241001518836 Monilinia fructigena Species 0.000 description 2
- JGFZNNIVVJXRND-UHFFFAOYSA-N N,N-Diisopropylethylamine (DIPEA) Chemical compound CCN(C(C)C)C(C)C JGFZNNIVVJXRND-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 2
- 235000002637 Nicotiana tabacum Nutrition 0.000 description 2
- 244000061176 Nicotiana tabacum Species 0.000 description 2
- 235000007164 Oryza sativa Nutrition 0.000 description 2
- 241000233622 Phytophthora infestans Species 0.000 description 2
- 241000233647 Phytophthora nicotianae var. parasitica Species 0.000 description 2
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
- 235000006040 Prunus persica var persica Nutrition 0.000 description 2
- 241000589623 Pseudomonas syringae pv. syringae Species 0.000 description 2
- 244000088401 Pyrus pyrifolia Species 0.000 description 2
- 235000001630 Pyrus pyrifolia var culta Nutrition 0.000 description 2
- 241000219492 Quercus Species 0.000 description 2
- 241000813090 Rhizoctonia solani Species 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical class [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 2
- 240000003768 Solanum lycopersicum Species 0.000 description 2
- 235000002597 Solanum melongena Nutrition 0.000 description 2
- 244000061458 Solanum melongena Species 0.000 description 2
- 241000187181 Streptomyces scabiei Species 0.000 description 2
- 235000021536 Sugar beet Nutrition 0.000 description 2
- 235000016639 Syzygium aromaticum Nutrition 0.000 description 2
- 244000223014 Syzygium aromaticum Species 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 235000021307 Triticum Nutrition 0.000 description 2
- 235000009754 Vitis X bourquina Nutrition 0.000 description 2
- 235000012333 Vitis X labruscana Nutrition 0.000 description 2
- 240000006365 Vitis vinifera Species 0.000 description 2
- 235000014787 Vitis vinifera Nutrition 0.000 description 2
- FJJCIZWZNKZHII-UHFFFAOYSA-N [4,6-bis(cyanoamino)-1,3,5-triazin-2-yl]cyanamide Chemical compound N#CNC1=NC(NC#N)=NC(NC#N)=N1 FJJCIZWZNKZHII-UHFFFAOYSA-N 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- PFKFTWBEEFSNDU-UHFFFAOYSA-N carbonyldiimidazole Chemical compound C1=CN=CN1C(=O)N1C=CN=C1 PFKFTWBEEFSNDU-UHFFFAOYSA-N 0.000 description 2
- 239000000969 carrier Substances 0.000 description 2
- 235000019693 cherries Nutrition 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- 239000012141 concentrate Substances 0.000 description 2
- 235000008504 concentrate Nutrition 0.000 description 2
- ZWWWLCMDTZFSOO-UHFFFAOYSA-N diethoxyphosphorylformonitrile Chemical compound CCOP(=O)(C#N)OCC ZWWWLCMDTZFSOO-UHFFFAOYSA-N 0.000 description 2
- USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical compound C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 description 2
- 201000010099 disease Diseases 0.000 description 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 2
- 239000007884 disintegrant Substances 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 235000013399 edible fruits Nutrition 0.000 description 2
- 239000003995 emulsifying agent Substances 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 239000012442 inert solvent Substances 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
- 239000007788 liquid Substances 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- SCVFZCLFOSHCOH-UHFFFAOYSA-M potassium acetate Chemical compound [K+].CC([O-])=O SCVFZCLFOSHCOH-UHFFFAOYSA-M 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 235000009566 rice Nutrition 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 239000000779 smoke Substances 0.000 description 2
- 229920005552 sodium lignosulfonate Polymers 0.000 description 2
- 239000002689 soil Substances 0.000 description 2
- 235000021012 strawberries Nutrition 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- 235000013616 tea Nutrition 0.000 description 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
- 239000000230 xanthan gum Substances 0.000 description 2
- 229920001285 xanthan gum Polymers 0.000 description 2
- 235000010493 xanthan gum Nutrition 0.000 description 2
- 229940082509 xanthan gum Drugs 0.000 description 2
- VMZBMTWFHYYOIN-UHFFFAOYSA-N (2-phenoxyphenyl)methanol Chemical compound OCC1=CC=CC=C1OC1=CC=CC=C1 VMZBMTWFHYYOIN-UHFFFAOYSA-N 0.000 description 1
- MEQOHPSGPWWTAM-UHFFFAOYSA-N (2-phenoxyphenyl)methyl 2-aminopyridine-3-carboxylate Chemical compound NC1=C(C(=O)OCC2=C(C=CC=C2)OC2=CC=CC=C2)C=CC=N1 MEQOHPSGPWWTAM-UHFFFAOYSA-N 0.000 description 1
- 125000004769 (C1-C4) alkylsulfonyl group Chemical group 0.000 description 1
- CYSGHNMQYZDMIA-UHFFFAOYSA-N 1,3-Dimethyl-2-imidazolidinon Chemical compound CN1CCN(C)C1=O CYSGHNMQYZDMIA-UHFFFAOYSA-N 0.000 description 1
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- DURPTKYDGMDSBL-UHFFFAOYSA-N 1-butoxybutane Chemical compound CCCCOCCCC DURPTKYDGMDSBL-UHFFFAOYSA-N 0.000 description 1
- 125000001478 1-chloroethyl group Chemical group [H]C([H])([H])C([H])(Cl)* 0.000 description 1
- HYZJCKYKOHLVJF-UHFFFAOYSA-N 1H-benzimidazole Chemical compound C1=CC=C2NC=NC2=C1 HYZJCKYKOHLVJF-UHFFFAOYSA-N 0.000 description 1
- 125000000453 2,2,2-trichloroethyl group Chemical group [H]C([H])(*)C(Cl)(Cl)Cl 0.000 description 1
- 125000004206 2,2,2-trifluoroethyl group Chemical group [H]C([H])(*)C(F)(F)F 0.000 description 1
- 125000004778 2,2-difluoroethyl group Chemical group [H]C([H])(*)C([H])(F)F 0.000 description 1
- 125000005999 2-bromoethyl group Chemical group 0.000 description 1
- 125000004780 2-chloro-2,2-difluoroethyl group Chemical group [H]C([H])(*)C(F)(F)Cl 0.000 description 1
- 125000001340 2-chloroethyl group Chemical group [H]C([H])(Cl)C([H])([H])* 0.000 description 1
- 125000004777 2-fluoroethyl group Chemical group [H]C([H])(F)C([H])([H])* 0.000 description 1
- AJBZENLMTKDAEK-UHFFFAOYSA-N 3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-4,9-diol Chemical compound CC12CCC(O)C(C)(C)C1CCC(C1(C)CC3O)(C)C2CCC1C1C3(C)CCC1C(=C)C AJBZENLMTKDAEK-UHFFFAOYSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- 235000003934 Abelmoschus esculentus Nutrition 0.000 description 1
- 240000004507 Abelmoschus esculentus Species 0.000 description 1
- 244000215068 Acacia senegal Species 0.000 description 1
- 241000208140 Acer Species 0.000 description 1
- 241001600124 Acidovorax avenae Species 0.000 description 1
- 235000009434 Actinidia chinensis Nutrition 0.000 description 1
- 244000298697 Actinidia deliciosa Species 0.000 description 1
- 235000009436 Actinidia deliciosa Nutrition 0.000 description 1
- 241000186361 Actinobacteria <class> Species 0.000 description 1
- ORILYTVJVMAKLC-UHFFFAOYSA-N Adamantane Natural products C1C(C2)CC3CC1CC2C3 ORILYTVJVMAKLC-UHFFFAOYSA-N 0.000 description 1
- 241000589176 Agrobacterium vitis Species 0.000 description 1
- 244000291564 Allium cepa Species 0.000 description 1
- 235000002732 Allium cepa var. cepa Nutrition 0.000 description 1
- 241000212251 Alternaria dauci Species 0.000 description 1
- 241000266416 Alternaria japonica Species 0.000 description 1
- 241000352690 Alternaria kikuchiana Species 0.000 description 1
- 241000323752 Alternaria longipes Species 0.000 description 1
- 241000412366 Alternaria mali Species 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- 206010001935 American trypanosomiasis Diseases 0.000 description 1
- 244000099147 Ananas comosus Species 0.000 description 1
- 240000001436 Antirrhinum majus Species 0.000 description 1
- 241001444083 Aphanomyces Species 0.000 description 1
- 240000007087 Apium graveolens Species 0.000 description 1
- 235000015849 Apium graveolens Dulce Group Nutrition 0.000 description 1
- 235000010591 Appio Nutrition 0.000 description 1
- 244000105624 Arachis hypogaea Species 0.000 description 1
- 240000005528 Arctium lappa Species 0.000 description 1
- 235000003130 Arctium lappa Nutrition 0.000 description 1
- 235000008078 Arctium minus Nutrition 0.000 description 1
- 235000000832 Ayote Nutrition 0.000 description 1
- 235000011274 Benincasa cerifera Nutrition 0.000 description 1
- 244000036905 Benincasa cerifera Species 0.000 description 1
- KXDAEFPNCMNJSK-UHFFFAOYSA-N Benzamide Chemical compound NC(=O)C1=CC=CC=C1 KXDAEFPNCMNJSK-UHFFFAOYSA-N 0.000 description 1
- 241000219495 Betulaceae Species 0.000 description 1
- 241001450781 Bipolaris oryzae Species 0.000 description 1
- 241001480061 Blumeria graminis Species 0.000 description 1
- 241000555706 Botryosphaeria dothidea Species 0.000 description 1
- 235000011293 Brassica napus Nutrition 0.000 description 1
- 240000007124 Brassica oleracea Species 0.000 description 1
- 235000003899 Brassica oleracea var acephala Nutrition 0.000 description 1
- 235000011301 Brassica oleracea var capitata Nutrition 0.000 description 1
- 235000001169 Brassica oleracea var oleracea Nutrition 0.000 description 1
- 235000010149 Brassica rapa subsp chinensis Nutrition 0.000 description 1
- 235000000536 Brassica rapa subsp pekinensis Nutrition 0.000 description 1
- 235000000540 Brassica rapa subsp rapa Nutrition 0.000 description 1
- 241000499436 Brassica rapa subsp. pekinensis Species 0.000 description 1
- 235000004977 Brassica sinapistrum Nutrition 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- 241000589638 Burkholderia glumae Species 0.000 description 1
- 241000134107 Burkholderia plantarii Species 0.000 description 1
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 1
- RDOXTESZEPMUJZ-UHFFFAOYSA-N COc1ccccc1 Chemical compound COc1ccccc1 RDOXTESZEPMUJZ-UHFFFAOYSA-N 0.000 description 1
- 235000003880 Calendula Nutrition 0.000 description 1
- 240000001432 Calendula officinalis Species 0.000 description 1
- 240000001548 Camellia japonica Species 0.000 description 1
- 235000002566 Capsicum Nutrition 0.000 description 1
- 240000004160 Capsicum annuum Species 0.000 description 1
- 235000008534 Capsicum annuum var annuum Nutrition 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- 235000009467 Carica papaya Nutrition 0.000 description 1
- 240000006432 Carica papaya Species 0.000 description 1
- 235000007763 Castanea pumila Nutrition 0.000 description 1
- 244000025797 Castanea pumila Species 0.000 description 1
- 241000530549 Cercospora beticola Species 0.000 description 1
- 241001658057 Cercospora kikuchii Species 0.000 description 1
- 208000024699 Chagas disease Diseases 0.000 description 1
- 240000005250 Chrysanthemum indicum Species 0.000 description 1
- 244000189548 Chrysanthemum x morifolium Species 0.000 description 1
- 244000241235 Citrullus lanatus Species 0.000 description 1
- 235000012828 Citrullus lanatus var citroides Nutrition 0.000 description 1
- 241000273649 Citrus hassaku Species 0.000 description 1
- 244000248349 Citrus limon Species 0.000 description 1
- 235000005979 Citrus limon Nutrition 0.000 description 1
- 240000004307 Citrus medica Species 0.000 description 1
- 241000555678 Citrus unshiu Species 0.000 description 1
- 240000000560 Citrus x paradisi Species 0.000 description 1
- 241000222290 Cladosporium Species 0.000 description 1
- 241001136168 Clavibacter michiganensis Species 0.000 description 1
- 241000222199 Colletotrichum Species 0.000 description 1
- 241000152100 Colletotrichum horii Species 0.000 description 1
- 241000222235 Colletotrichum orbiculare Species 0.000 description 1
- 241000998302 Colletotrichum tabaci Species 0.000 description 1
- 241001584859 Colocasia <moth> Species 0.000 description 1
- 235000009854 Cucurbita moschata Nutrition 0.000 description 1
- 240000001980 Cucurbita pepo Species 0.000 description 1
- 235000009804 Cucurbita pepo subsp pepo Nutrition 0.000 description 1
- 241000371644 Curvularia ravenelii Species 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- 235000012040 Dahlia pinnata Nutrition 0.000 description 1
- 244000033273 Dahlia variabilis Species 0.000 description 1
- 241001645342 Diaporthe citri Species 0.000 description 1
- 241001508801 Diaporthe phaseolorum Species 0.000 description 1
- ZAFNJMIOTHYJRJ-UHFFFAOYSA-N Diisopropyl ether Chemical compound CC(C)OC(C)C ZAFNJMIOTHYJRJ-UHFFFAOYSA-N 0.000 description 1
- 241000663351 Diplocarpon rosae Species 0.000 description 1
- 241000125117 Elsinoe Species 0.000 description 1
- 241000901048 Elsinoe ampelina Species 0.000 description 1
- 241001568757 Elsinoe glycines Species 0.000 description 1
- 241001564064 Elsinoe theae Species 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 235000009008 Eriobotrya japonica Nutrition 0.000 description 1
- 244000061508 Eriobotrya japonica Species 0.000 description 1
- 241000510928 Erysiphe necator Species 0.000 description 1
- 241001489205 Erysiphe pisi Species 0.000 description 1
- 240000002395 Euphorbia pulcherrima Species 0.000 description 1
- 241001411323 Exobasidium reticulatum Species 0.000 description 1
- 241000233866 Fungi Species 0.000 description 1
- 241000223195 Fusarium graminearum Species 0.000 description 1
- 241000223221 Fusarium oxysporum Species 0.000 description 1
- 241000735356 Gazania Species 0.000 description 1
- 241000735332 Gerbera Species 0.000 description 1
- 244000068988 Glycine max Species 0.000 description 1
- 229920000084 Gum arabic Polymers 0.000 description 1
- 241001194823 Gymnosporangium asiaticum Species 0.000 description 1
- 241001540851 Gymnosporangium yamadae Species 0.000 description 1
- 235000008694 Humulus lupulus Nutrition 0.000 description 1
- 244000025221 Humulus lupulus Species 0.000 description 1
- 244000267823 Hydrangea macrophylla Species 0.000 description 1
- 235000014486 Hydrangea macrophylla Nutrition 0.000 description 1
- 244000017020 Ipomoea batatas Species 0.000 description 1
- 235000002678 Ipomoea batatas Nutrition 0.000 description 1
- 240000008415 Lactuca sativa Species 0.000 description 1
- 240000007472 Leucaena leucocephala Species 0.000 description 1
- 235000010643 Leucaena leucocephala Nutrition 0.000 description 1
- 241000896221 Leveillula taurica Species 0.000 description 1
- WLLGXSLBOPFWQV-UHFFFAOYSA-N MGK 264 Chemical compound C1=CC2CC1C1C2C(=O)N(CC(CC)CCCC)C1=O WLLGXSLBOPFWQV-UHFFFAOYSA-N 0.000 description 1
- 241001330975 Magnaporthe oryzae Species 0.000 description 1
- 244000081841 Malus domestica Species 0.000 description 1
- 244000070406 Malus silvestris Species 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 235000009811 Momordica charantia Nutrition 0.000 description 1
- 244000302512 Momordica charantia Species 0.000 description 1
- 241001363493 Monilinia mali Species 0.000 description 1
- 241001459558 Monographella nivalis Species 0.000 description 1
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 1
- 241000083073 Neopseudocercosporella capsellae Species 0.000 description 1
- 239000000020 Nitrocellulose Substances 0.000 description 1
- 241001329956 Nothopassalora personata Species 0.000 description 1
- PZVJBPOXOUZXPK-UHFFFAOYSA-N O=C(c1c(C(F)(F)F)ccnc1)OC(c1cccc2c1cccc2)c1cnccc1C(F)(F)F Chemical compound O=C(c1c(C(F)(F)F)ccnc1)OC(c1cccc2c1cccc2)c1cnccc1C(F)(F)F PZVJBPOXOUZXPK-UHFFFAOYSA-N 0.000 description 1
- 241001668536 Oculimacula yallundae Species 0.000 description 1
- 241000315044 Passalora arachidicola Species 0.000 description 1
- 241000222291 Passalora fulva Species 0.000 description 1
- 241001507673 Penicillium digitatum Species 0.000 description 1
- 241000582441 Peronospora tabacina Species 0.000 description 1
- 244000025272 Persea americana Species 0.000 description 1
- 235000008673 Persea americana Nutrition 0.000 description 1
- 244000062780 Petroselinum sativum Species 0.000 description 1
- 240000007377 Petunia x hybrida Species 0.000 description 1
- 241001098206 Phakopsora ampelopsidis Species 0.000 description 1
- 235000006089 Phaseolus angularis Nutrition 0.000 description 1
- 241000746983 Phleum pratense Species 0.000 description 1
- 241001557902 Phomopsis sp. Species 0.000 description 1
- 241000257732 Phomopsis vexans Species 0.000 description 1
- 241000210649 Phyllosticta ampelicida Species 0.000 description 1
- 241000555714 Phyllosticta citricarpa Species 0.000 description 1
- 241001270527 Phyllosticta citrullina Species 0.000 description 1
- 241000233631 Phytophthora citrophthora Species 0.000 description 1
- 241000031556 Phytophthora sp. Species 0.000 description 1
- 241000758706 Piperaceae Species 0.000 description 1
- 241001281803 Plasmopara viticola Species 0.000 description 1
- 241000317981 Podosphaera fuliginea Species 0.000 description 1
- 241001337928 Podosphaera leucotricha Species 0.000 description 1
- 241001294742 Podosphaera macularis Species 0.000 description 1
- 241000896203 Podosphaera pannosa Species 0.000 description 1
- 229920001213 Polysorbate 20 Polymers 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
- 235000009827 Prunus armeniaca Nutrition 0.000 description 1
- 244000018633 Prunus armeniaca Species 0.000 description 1
- 244000018795 Prunus mume Species 0.000 description 1
- 235000006029 Prunus persica var nucipersica Nutrition 0.000 description 1
- 244000017714 Prunus persica var. nucipersica Species 0.000 description 1
- 241000301598 Pseudocercospora kaki Species 0.000 description 1
- 241000521936 Pseudomonas amygdali pv. lachrymans Species 0.000 description 1
- 241000218936 Pseudomonas corrugata Species 0.000 description 1
- 241000490004 Pseudomonas fuscovaginae Species 0.000 description 1
- 241000394642 Pseudomonas marginalis pv. marginalis Species 0.000 description 1
- 241000589612 Pseudomonas savastanoi pv. glycinea Species 0.000 description 1
- 241000589613 Pseudomonas savastanoi pv. phaseolicola Species 0.000 description 1
- 241001487783 Pseudomonas syringae pv. theae Species 0.000 description 1
- 241001281805 Pseudoperonospora cubensis Species 0.000 description 1
- 241001246058 Puccinia allii Species 0.000 description 1
- 241000221301 Puccinia graminis Species 0.000 description 1
- 241001123559 Puccinia hordei Species 0.000 description 1
- 241000312975 Puccinia horiana Species 0.000 description 1
- 241001123569 Puccinia recondita Species 0.000 description 1
- 241001123583 Puccinia striiformis Species 0.000 description 1
- 241000520648 Pyrenophora teres Species 0.000 description 1
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 description 1
- 235000014443 Pyrus communis Nutrition 0.000 description 1
- 240000001987 Pyrus communis Species 0.000 description 1
- 241001385948 Pythium sp. Species 0.000 description 1
- 244000088415 Raphanus sativus Species 0.000 description 1
- 235000006140 Raphanus sativus var sativus Nutrition 0.000 description 1
- 241000022649 Rhizobacter dauci Species 0.000 description 1
- 241000208422 Rhododendron Species 0.000 description 1
- 235000004789 Rosa xanthina Nutrition 0.000 description 1
- 241000109329 Rosa xanthina Species 0.000 description 1
- 244000178231 Rosmarinus officinalis Species 0.000 description 1
- 240000000111 Saccharum officinarum Species 0.000 description 1
- 235000007201 Saccharum officinarum Nutrition 0.000 description 1
- 241000124033 Salix Species 0.000 description 1
- 241000221696 Sclerotinia sclerotiorum Species 0.000 description 1
- 241000336765 Septoria chrysanthemella Species 0.000 description 1
- 240000003461 Setaria viridis Species 0.000 description 1
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 1
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- VBIIFPGSPJYLRR-UHFFFAOYSA-M Stearyltrimethylammonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[N+](C)(C)C VBIIFPGSPJYLRR-UHFFFAOYSA-M 0.000 description 1
- 241000142909 Streptomyces acidiscabies Species 0.000 description 1
- 229930182692 Strobilurin Natural products 0.000 description 1
- ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical class OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 description 1
- 235000004338 Syringa vulgaris Nutrition 0.000 description 1
- 244000297179 Syringa vulgaris Species 0.000 description 1
- 235000006468 Thea sinensis Nutrition 0.000 description 1
- 241000722093 Tilletia caries Species 0.000 description 1
- 241000223109 Trypanosoma cruzi Species 0.000 description 1
- 241000051572 Typhula sp. Species 0.000 description 1
- 241000007070 Ustilago nuda Species 0.000 description 1
- 241000233791 Ustilago tritici Species 0.000 description 1
- 241001512566 Valsa mali Species 0.000 description 1
- 241001669640 Venturia carpophila Species 0.000 description 1
- 241000228452 Venturia inaequalis Species 0.000 description 1
- 241001669638 Venturia nashicola Species 0.000 description 1
- 241001006642 Venturia pyrina Species 0.000 description 1
- 235000007212 Verbena X moechina Moldenke Nutrition 0.000 description 1
- 240000001519 Verbena officinalis Species 0.000 description 1
- 235000001594 Verbena polystachya Kunth Nutrition 0.000 description 1
- 235000007200 Verbena x perriana Moldenke Nutrition 0.000 description 1
- 235000002270 Verbena x stuprosa Moldenke Nutrition 0.000 description 1
- 241000219977 Vigna Species 0.000 description 1
- 235000010711 Vigna angularis Nutrition 0.000 description 1
- 240000007098 Vigna angularis Species 0.000 description 1
- 241000985670 Xanthomonas arboricola pv. pruni Species 0.000 description 1
- 241000589655 Xanthomonas citri Species 0.000 description 1
- 241001517731 Xanthomonas citri pv. glycines Species 0.000 description 1
- 241000231754 Xanthomonas fragariae Species 0.000 description 1
- 241000907138 Xanthomonas oryzae pv. oryzae Species 0.000 description 1
- 241000194062 Xanthomonas phaseoli Species 0.000 description 1
- 241000567011 Xanthomonas theicola Species 0.000 description 1
- 240000008042 Zea mays Species 0.000 description 1
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 1
- 241000190020 Zelkova serrata Species 0.000 description 1
- 239000000205 acacia gum Substances 0.000 description 1
- 235000010489 acacia gum Nutrition 0.000 description 1
- 150000001242 acetic acid derivatives Chemical class 0.000 description 1
- KXKVLQRXCPHEJC-UHFFFAOYSA-N acetic acid trimethyl ester Natural products COC(C)=O KXKVLQRXCPHEJC-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000000443 aerosol Substances 0.000 description 1
- 150000004703 alkoxides Chemical class 0.000 description 1
- 150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
- 125000005037 alkyl phenyl group Chemical group 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 239000002280 amphoteric surfactant Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000000440 bentonite Substances 0.000 description 1
- 229910000278 bentonite Inorganic materials 0.000 description 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 150000003857 carboxamides Chemical class 0.000 description 1
- 239000003093 cationic surfactant Substances 0.000 description 1
- 235000013339 cereals Nutrition 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- AOGYCOYQMAVAFD-UHFFFAOYSA-N chlorocarbonic acid Chemical class OC(Cl)=O AOGYCOYQMAVAFD-UHFFFAOYSA-N 0.000 description 1
- 235000020971 citrus fruits Nutrition 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 238000004440 column chromatography Methods 0.000 description 1
- 208000030499 combat disease Diseases 0.000 description 1
- 235000018597 common camellia Nutrition 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 235000009508 confectionery Nutrition 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 235000005822 corn Nutrition 0.000 description 1
- 150000004292 cyclic ethers Chemical class 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical compound O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 description 1
- 125000004783 dichloromethoxy group Chemical group ClC(O*)Cl 0.000 description 1
- 125000004772 dichloromethyl group Chemical group [H]C(Cl)(Cl)* 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 125000001028 difluoromethyl group Chemical group [H]C(F)(F)* 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 229960000878 docusate sodium Drugs 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 238000003912 environmental pollution Methods 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 125000006125 ethylsulfonyl group Chemical group 0.000 description 1
- 125000004705 ethylthio group Chemical group C(C)S* 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- 235000019197 fats Nutrition 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000010433 feldspar Substances 0.000 description 1
- 239000003337 fertilizer Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 125000001153 fluoro group Chemical group F* 0.000 description 1
- 125000004995 haloalkylthio group Chemical group 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 238000003306 harvesting Methods 0.000 description 1
- 125000006341 heptafluoro n-propyl group Chemical group FC(F)(F)C(F)(F)C(F)(F)* 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-M hexanoate Chemical compound CCCCCC([O-])=O FUZZWVXGSFPDMH-UHFFFAOYSA-M 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 150000007529 inorganic bases Chemical class 0.000 description 1
- 239000013067 intermediate product Substances 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 229910052622 kaolinite Inorganic materials 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 229940094506 lauryl betaine Drugs 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- 230000003902 lesion Effects 0.000 description 1
- 235000014666 liquid concentrate Nutrition 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- 125000002816 methylsulfanyl group Chemical group [H]C([H])([H])S[*] 0.000 description 1
- 125000006216 methylsulfinyl group Chemical group [H]C([H])([H])S(*)=O 0.000 description 1
- 125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 description 1
- 229910052901 montmorillonite Inorganic materials 0.000 description 1
- PSHKMPUSSFXUIA-UHFFFAOYSA-N n,n-dimethylpyridin-2-amine Chemical compound CN(C)C1=CC=CC=N1 PSHKMPUSSFXUIA-UHFFFAOYSA-N 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- DVEKCXOJTLDBFE-UHFFFAOYSA-N n-dodecyl-n,n-dimethylglycinate Chemical compound CCCCCCCCCCCC[N+](C)(C)CC([O-])=O DVEKCXOJTLDBFE-UHFFFAOYSA-N 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical compound C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 229920001220 nitrocellulos Polymers 0.000 description 1
- 125000006344 nonafluoro n-butyl group Chemical group FC(F)(F)C(F)(F)C(F)(F)C(F)(F)* 0.000 description 1
- 239000012044 organic layer Substances 0.000 description 1
- 235000020232 peanut Nutrition 0.000 description 1
- 239000003415 peat Substances 0.000 description 1
- 125000006340 pentafluoro ethyl group Chemical group FC(F)(F)C(F)(F)* 0.000 description 1
- 235000011197 perejil Nutrition 0.000 description 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
- CKFBFQHBUCDOHL-UHFFFAOYSA-N phenoxy(phenyl)methanol Chemical class C=1C=CC=CC=1C(O)OC1=CC=CC=C1 CKFBFQHBUCDOHL-UHFFFAOYSA-N 0.000 description 1
- 230000003032 phytopathogenic effect Effects 0.000 description 1
- 239000005648 plant growth regulator Substances 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 239000000256 polyoxyethylene sorbitan monolaurate Substances 0.000 description 1
- 235000010486 polyoxyethylene sorbitan monolaurate Nutrition 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 235000011056 potassium acetate Nutrition 0.000 description 1
- 239000011736 potassium bicarbonate Substances 0.000 description 1
- 229910000028 potassium bicarbonate Inorganic materials 0.000 description 1
- 235000015497 potassium bicarbonate Nutrition 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 235000011181 potassium carbonates Nutrition 0.000 description 1
- TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 description 1
- 229940086066 potassium hydrogencarbonate Drugs 0.000 description 1
- 235000011118 potassium hydroxide Nutrition 0.000 description 1
- LPNYRYFBWFDTMA-UHFFFAOYSA-N potassium tert-butoxide Chemical compound [K+].CC(C)(C)[O-] LPNYRYFBWFDTMA-UHFFFAOYSA-N 0.000 description 1
- 239000003380 propellant Substances 0.000 description 1
- 235000015136 pumpkin Nutrition 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 235000002020 sage Nutrition 0.000 description 1
- 235000012045 salad Nutrition 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 238000010898 silica gel chromatography Methods 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 239000001632 sodium acetate Substances 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 235000017550 sodium carbonate Nutrition 0.000 description 1
- APSBXTVYXVQYAB-UHFFFAOYSA-M sodium docusate Chemical compound [Na+].CCCCC(CC)COC(=O)CC(S([O-])(=O)=O)C(=O)OCC(CC)CCCC APSBXTVYXVQYAB-UHFFFAOYSA-M 0.000 description 1
- QDRKDTQENPPHOJ-UHFFFAOYSA-N sodium ethoxide Chemical compound [Na+].CC[O-] QDRKDTQENPPHOJ-UHFFFAOYSA-N 0.000 description 1
- 235000011121 sodium hydroxide Nutrition 0.000 description 1
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 239000003516 soil conditioner Substances 0.000 description 1
- 239000004550 soluble concentrate Substances 0.000 description 1
- 238000009331 sowing Methods 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 125000000446 sulfanediyl group Chemical group *S* 0.000 description 1
- 150000003462 sulfoxides Chemical class 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 239000003826 tablet Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 229940124597 therapeutic agent Drugs 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 150000003852 triazoles Chemical class 0.000 description 1
- 125000004784 trichloromethoxy group Chemical group ClC(O*)(Cl)Cl 0.000 description 1
- 125000003866 trichloromethyl group Chemical group ClC(Cl)(Cl)* 0.000 description 1
- 125000005034 trifluormethylthio group Chemical group FC(S*)(F)F 0.000 description 1
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 description 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 239000004562 water dispersible granule Substances 0.000 description 1
- 239000004552 water soluble powder Substances 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D221/00—Heterocyclic compounds containing six-membered rings having one nitrogen atom as the only ring hetero atom, not provided for by groups C07D211/00 - C07D219/00
- C07D221/02—Heterocyclic compounds containing six-membered rings having one nitrogen atom as the only ring hetero atom, not provided for by groups C07D211/00 - C07D219/00 condensed with carbocyclic rings or ring systems
- C07D221/04—Ortho- or peri-condensed ring systems
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
- A01N43/42—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings condensed with carbocyclic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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
- C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/79—Acids; Esters
- C07D213/80—Acids; Esters in position 3
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom 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
- C07D215/48—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
- C07D215/54—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen attached in position 3
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Environmental Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Plant Pathology (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Pyridine Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2012150421 | 2012-07-04 | ||
| JP2012-150421 | 2012-07-04 | ||
| PCT/JP2013/060061 WO2014006945A1 (ja) | 2012-07-04 | 2013-04-02 | 2-アミノニコチン酸エステル誘導体およびこれを有効成分とする殺菌剤 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| RU2015103515A RU2015103515A (ru) | 2016-08-20 |
| RU2599725C2 true RU2599725C2 (ru) | 2016-10-10 |
Family
ID=49881710
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| RU2015103515/04A RU2599725C2 (ru) | 2012-07-04 | 2013-04-02 | Производное соединение сложного эфира 2-аминоникотиновой кислоты и бактерицид, содержащий то же самое в качестве активного ингредиента |
Country Status (20)
| Country | Link |
|---|---|
| US (1) | US9096528B2 (enExample) |
| EP (1) | EP2871180B1 (enExample) |
| JP (1) | JP6114958B2 (enExample) |
| KR (1) | KR101629767B1 (enExample) |
| CN (1) | CN104520273B (enExample) |
| AU (1) | AU2013284775B2 (enExample) |
| BR (1) | BR112014032873B1 (enExample) |
| CA (1) | CA2877235C (enExample) |
| CL (1) | CL2014003643A1 (enExample) |
| CO (1) | CO7240428A2 (enExample) |
| ES (1) | ES2665561T3 (enExample) |
| HU (1) | HUE037765T2 (enExample) |
| IN (1) | IN2014DN10806A (enExample) |
| MA (1) | MA37825B1 (enExample) |
| PL (1) | PL2871180T3 (enExample) |
| PT (1) | PT2871180T (enExample) |
| RU (1) | RU2599725C2 (enExample) |
| UA (1) | UA111542C2 (enExample) |
| WO (1) | WO2014006945A1 (enExample) |
| ZA (1) | ZA201500742B (enExample) |
Families Citing this family (237)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP6212773B2 (ja) * | 2013-08-01 | 2017-10-18 | アグロカネショウ株式会社 | ２−アミノニコチン酸ベンジル誘導体およびこれを有効成分とする殺菌剤 |
| WO2015060378A1 (ja) * | 2013-10-25 | 2015-04-30 | 日本曹達株式会社 | アミノピリジン誘導体および農園芸用殺菌剤 |
| JP6286693B2 (ja) * | 2013-12-25 | 2018-03-07 | アグロカネショウ株式会社 | ６−置換ニコチン酸エステル誘導体およびこれを有効成分とする殺菌剤 |
| KR101728443B1 (ko) | 2013-12-27 | 2017-04-19 | 아구로카네쇼 가부시키가이샤 | 2-아미노니코틴산벤질에스테르 유도체의 제조 방법 |
| JP6331075B2 (ja) * | 2014-04-11 | 2018-05-30 | アグロカネショウ株式会社 | ３−アミノ−１ｈ−ピラゾール−４−カルボン酸ベンジルエステル誘導体およびこれを有効成分とする殺菌剤 |
| JPWO2015190601A1 (ja) * | 2014-06-13 | 2017-04-20 | アグロカネショウ株式会社 | ２−アシルアミノニコチン酸エステル誘導体およびこれを有効成分とする殺菌剤 |
| RU2658916C1 (ru) | 2014-06-27 | 2018-06-26 | Агро-Канесо Ко., Лтд. | Способ получения 2-амино-6-метилникотиновой кислоты |
| JP6331084B2 (ja) * | 2014-06-30 | 2018-05-30 | アグロカネショウ株式会社 | ２−ベンジルアミノニコチン酸エステル誘導体およびこれを有効成分とする殺菌剤 |
| JP2017197433A (ja) * | 2014-09-12 | 2017-11-02 | 石原産業株式会社 | ニコチン酸エステル化合物、農園芸用殺菌剤及び植物病害の防除方法 |
| WO2017126197A1 (ja) * | 2016-01-21 | 2017-07-27 | アグロカネショウ株式会社 | ２－アミノニコチン酸ベンジルエステル誘導体の製造方法 |
| TWI760428B (zh) | 2017-01-26 | 2022-04-11 | 日商三井化學Agro股份有限公司 | 吡啶酮化合物及以吡啶酮化合物作為有效成分的農園藝用殺菌劑 |
| WO2018190351A1 (ja) | 2017-04-10 | 2018-10-18 | 三井化学アグロ株式会社 | ピリドン化合物およびそれを有効成分とする農園芸用殺菌剤 |
| JP7168556B2 (ja) | 2017-04-10 | 2022-11-09 | 三井化学アグロ株式会社 | ピリドン化合物およびそれを有効成分とする農園芸用殺菌剤 |
| EP3611165B1 (en) | 2017-04-11 | 2023-08-16 | Mitsui Chemicals Crop & Life Solutions, Inc. | Pyridone compound, and agricultural and horticultural fungicide having this as active component |
| JP7157738B2 (ja) | 2017-06-08 | 2022-10-20 | 三井化学アグロ株式会社 | ピリドン化合物およびそれを有効成分とする農園芸用殺菌剤 |
| WO2019007717A1 (en) * | 2017-07-06 | 2019-01-10 | Basf Se | PESTICIDE MIXTURES |
| CN110590653B (zh) * | 2018-06-12 | 2021-01-12 | 浙江省化工研究院有限公司 | 一种烟酸酯类化合物、其制备方法及应用 |
| JP7291143B2 (ja) | 2018-07-25 | 2023-06-14 | 三井化学クロップ＆ライフソリューション株式会社 | ピリドン化合物およびそれを有効成分とする農園芸用殺菌剤 |
| GB201812692D0 (en) | 2018-08-03 | 2018-09-19 | Syngenta Participations Ag | Microbiocidal compounds |
| TW202019901A (zh) | 2018-09-13 | 2020-06-01 | 瑞士商先正達合夥公司 | 殺有害生物活性唑-醯胺化合物 |
| TW202023386A (zh) | 2018-09-13 | 2020-07-01 | 瑞士商先正達合夥公司 | 殺有害生物活性唑-醯胺化合物 |
| AR116628A1 (es) | 2018-10-18 | 2021-05-26 | Syngenta Crop Protection Ag | Compuestos microbiocidas |
| TW202033512A (zh) | 2018-10-19 | 2020-09-16 | 瑞士商先正達農作物保護公司 | 殺有害生物活性唑-醯胺化合物 |
| JP2022509019A (ja) | 2018-11-05 | 2022-01-20 | シンジェンタ パーティシペーションズ アーゲー | 殺有害生物的に活性なアゾール－アミド化合物 |
| AR117183A1 (es) | 2018-11-30 | 2021-07-14 | Syngenta Crop Protection Ag | Derivados de tiazol microbiocidas |
| AR117200A1 (es) | 2018-11-30 | 2021-07-21 | Syngenta Participations Ag | Derivados de tiazol microbiocidas |
| WO2020165403A1 (en) | 2019-02-15 | 2020-08-20 | Syngenta Crop Protection Ag | Phenyl substituted thiazole derivatives as microbiocidal compounds |
| EP3696175A1 (en) | 2019-02-18 | 2020-08-19 | Syngenta Crop Protection AG | Pesticidally active azole-amide compounds |
| WO2020169526A1 (en) | 2019-02-18 | 2020-08-27 | Syngenta Crop Protection Ag | Pesticidally-active cyanamide heterocyclic compounds |
| ES2953140T3 (es) | 2019-03-08 | 2023-11-08 | Syngenta Crop Protection Ag | Compuestos de azol-amida activos de manera plaguicida |
| CN113597424B (zh) | 2019-03-20 | 2025-04-18 | 先正达农作物保护股份公司 | 杀有害生物活性的唑酰胺化合物 |
| JP2022525967A (ja) | 2019-03-20 | 2022-05-20 | シンジェンタ クロップ プロテクション アクチェンゲゼルシャフト | 殺有害生物活性アゾールアミド化合物 |
| BR112021018822A2 (pt) | 2019-03-22 | 2021-11-23 | Syngenta Crop Protection Ag | Derivados de n-[1-(5-bromo-2-pirimidin-2-il-1,2,4-triazol-3-il)etil]-2-ciclopropil-6-(trifluorometil)piridina-4-carboxamida e compostos relacionados como inseticidas |
| GB201903942D0 (en) | 2019-03-22 | 2019-05-08 | Syngenta Crop Protection Ag | Microbiocidal compounds |
| JP7472163B2 (ja) | 2019-03-27 | 2024-04-22 | シンジェンタ クロップ プロテクション アクチェンゲゼルシャフト | 殺微生物性チアゾール誘導体 |
| TWI853009B (zh) | 2019-03-29 | 2024-08-21 | 瑞士商先正達農作物保護公司 | 殺有害生物活性之二-醯胺化合物 |
| BR112021019987A2 (pt) | 2019-04-05 | 2021-12-07 | Syngenta Crop Protection Ag | Compostos de diazina-amida pesticidamente ativos |
| BR112021020240A2 (pt) | 2019-04-10 | 2021-12-07 | Syngenta Crop Protection Ag | Composições fungicidas |
| WO2020208095A1 (en) | 2019-04-10 | 2020-10-15 | Syngenta Crop Protection Ag | Microbiocidal picolinamide derivatives |
| WO2020208036A1 (en) | 2019-04-11 | 2020-10-15 | Syngenta Crop Protection Ag | Pesticidally active diazine-amide compounds |
| CN113939510A (zh) | 2019-05-29 | 2022-01-14 | 先正达农作物保护股份公司 | 杀微生物衍生物 |
| CN113924294B (zh) | 2019-05-29 | 2024-12-06 | 先正达农作物保护股份公司 | 杀微生物衍生物 |
| AR119011A1 (es) | 2019-05-29 | 2021-11-17 | Syngenta Crop Protection Ag | DERIVADOS DE [1,3]DIOXOLO[4,5-c]PIRIDIN-4-CARBOXAMIDA, COMPOSICIONES AGROQUÍMICAS QUE LOS COMPRENDEN Y SU EMPLEO COMO FUNGICIDA PARA CONTROLAR O PREVENIR LA INFESTACIÓN DE PLANTAS ÚTILES |
| AR119009A1 (es) | 2019-05-29 | 2021-11-17 | Syngenta Crop Protection Ag | Derivados de alcoxipiridina y alcoxipirimidina microbicidas |
| WO2020254530A1 (en) | 2019-06-18 | 2020-12-24 | Syngenta Crop Protection Ag | 7-sulfonyl-n-(1,3,4-thiadiazol-2-yl)-quinoxaline-6-carboxamide derivatives and the respective -benzimidazole-5-, -imidazo[4,5-b]pyridine-5-, -3h-furo[3,2b]pyridine-5-, -quinoline-2-, and -naphthalene-2-carboxamide derivatives as pesticides |
| BR112021026861A2 (pt) | 2019-07-05 | 2022-02-22 | Syngenta Crop Protection Ag | Derivados de picolinamida microbiocidas |
| GB201910037D0 (en) | 2019-07-12 | 2019-08-28 | Syngenta Crop Protection Ag | Microbiocidal compounds |
| CA3147089A1 (en) | 2019-08-21 | 2021-02-25 | Jamie RICKARD | Sowing device and method for treating seeds during planting |
| BR112022003177A2 (pt) | 2019-08-21 | 2022-05-17 | Syngenta Participations Ag | Aparelho e método para reduzir o desenvolvimento de poeira na semeadura por perfuração de precisão |
| EP4017241A1 (en) | 2019-08-21 | 2022-06-29 | Syngenta Participations Ag | Precision treatment and sowing or planting method and device |
| EP4017242A1 (en) | 2019-08-21 | 2022-06-29 | Syngenta Participations Ag | Apparatus and method for converting existing sowing equipment |
| CA3147138A1 (en) | 2019-08-21 | 2021-02-25 | Jamie RICKARD | High precision greenhouse seed and seedling treatment |
| CN114269732A (zh) | 2019-08-23 | 2022-04-01 | 先正达农作物保护股份公司 | 杀有害生物活性的吡嗪-酰胺化合物 |
| GB201912595D0 (en) | 2019-09-02 | 2019-10-16 | Syngenta Crop Protection Ag | Plant growth regulator compounds |
| BR112022005137A2 (pt) | 2019-09-20 | 2022-06-14 | Syngenta Crop Protection Ag | Derivados heterocíclicos com substituintes contendo enxofre e sulfoximina ativos em termos pesticidas |
| UY38885A (es) | 2019-09-20 | 2021-04-30 | Syngenta Crop Protection Ag | Compuestos de azetidinil-, pirrolidinil-,piperdinil- o piperazinil-piridinil carbonilo pesticidamente activos |
| IL291996B1 (en) | 2019-11-01 | 2025-09-01 | Syngenta Crop Protection Ag | Molten bicyclic heteroaromatic compounds active as pesticides |
| EP4069688B1 (en) | 2019-12-04 | 2025-10-01 | Syngenta Crop Protection AG | Pesticidally active fused bicyclic heteroaromatic amino compounds |
| WO2021122645A1 (en) | 2019-12-20 | 2021-06-24 | Syngenta Crop Protection Ag | Pesticidally active azole-amide compounds |
| WO2021136722A1 (en) | 2019-12-31 | 2021-07-08 | Syngenta Crop Protection Ag | Pesticidally active heterocyclic derivatives with sulfur containing substituents |
| TW202132300A (zh) | 2020-01-06 | 2021-09-01 | 瑞士商先正達農作物保護公司 | 具有含硫取代基的殺有害生物活性雜環衍生物 |
| WO2021144354A1 (en) | 2020-01-15 | 2021-07-22 | Syngenta Crop Protection Ag | Pesticidally-active bicyclic heteroaromatic compounds |
| EP4093735A1 (en) | 2020-01-24 | 2022-11-30 | Syngenta Crop Protection AG | Pesticidally active fused bicyclic heteroaromatic compounds |
| US20230142606A1 (en) | 2020-01-30 | 2023-05-11 | Syngenta Crop Protection Ag | Pesticidally active fused bicyclic heteroaromatic amino compounds |
| EP4103549A1 (en) | 2020-02-11 | 2022-12-21 | Syngenta Crop Protection AG | Pesticidally active cyclic amine compounds |
| BR112022017093A2 (pt) | 2020-02-27 | 2023-02-14 | Syngenta Crop Protection Ag | Compostos de diazina-bisamida ativos em termos pesticidas |
| WO2021175822A1 (en) | 2020-03-02 | 2021-09-10 | Syngenta Crop Protection Ag | Pesticidally amidine-substituted benzoic acid amide compounds |
| US20230131427A1 (en) | 2020-03-05 | 2023-04-27 | Syngenta Crop Protection Ag | Fungicidal compositions |
| UY39115A (es) | 2020-03-05 | 2021-10-29 | Syngenta Crop Protection Ag | Mezclas fungicidas de derivados de arilo metoxiacrilato |
| US20230126361A1 (en) | 2020-03-13 | 2023-04-27 | Syngenta Crop Protection Ag | Methods of controlling or preventing infestation of plants by the phytopathogenic microorganism corynespora cassiicola, cercospora sojina and/or cercospora kikuchii |
| US20230111656A1 (en) | 2020-03-13 | 2023-04-13 | Syngenta Crop Protection Ag | Methods of controlling or preventing infestation of soybean plants by the phytopathogenic microorganism corynespora cassiicola |
| CN115243547A (zh) | 2020-03-13 | 2022-10-25 | 先正达农作物保护股份公司 | 控制或预防植物被植物病原性微生物多主棒孢菌侵染的方法 |
| WO2021180975A1 (en) | 2020-03-13 | 2021-09-16 | Syngenta Crop Protection Ag | Methods of controlling or preventing infestation of plants by the phytopathogenic microorganism corynespora cassiicola |
| BR112022018280A2 (pt) | 2020-03-13 | 2022-10-25 | Syngenta Crop Protection Ag | Métodos de controle ou prevenção de infestação de plantas pelo microrganismo fitopatogênico corynespora cassiicola |
| WO2021180598A1 (en) | 2020-03-13 | 2021-09-16 | Syngenta Crop Protection Ag | Methods of controlling or preventing infestation of plants by the phytopathogenic microorganism corynespora cassiicola |
| AR121734A1 (es) | 2020-04-08 | 2022-07-06 | Syngenta Crop Protection Ag | Derivados microbicidas de tipo dihidropirrolopirazina de quinolina |
| AR121733A1 (es) | 2020-04-08 | 2022-07-06 | Syngenta Crop Protection Ag | Derivados microbiocidas de tipo dihidro-(tiazina)oxazina de quinolina |
| EP4132924B1 (en) | 2020-04-08 | 2024-02-21 | Syngenta Crop Protection AG | Microbiocidal quinoline dihydro-(thiazine)oxazine derivatives |
| WO2021213929A1 (en) | 2020-04-20 | 2021-10-28 | Syngenta Crop Protection Ag | Pesticidally active substituted 1,3-dihydro-2h-imidazo[4,5-c]pyridin-2-one derivatives with sulfur containing substituents |
| US20230167122A1 (en) | 2020-04-30 | 2023-06-01 | Syngenta Crop Protection Ag | Pesticidally active heterocyclic derivatives with sulfur containing substituents |
| GB202006399D0 (en) | 2020-04-30 | 2020-06-17 | Syngenta Crop Protection Ag | Microbiocidal compounds |
| GB202006386D0 (en) | 2020-04-30 | 2020-06-17 | Syngenta Crop Protection Ag | Microbiocidal Compounds |
| GB202006480D0 (en) | 2020-05-01 | 2020-06-17 | Syngenta Crop Protection Ag | Microbiocidal compounds |
| GB202006606D0 (en) | 2020-05-05 | 2020-06-17 | Syngenta Crop Protection Ag | Microbiocidal compounds |
| WO2021224409A1 (en) | 2020-05-06 | 2021-11-11 | Syngenta Crop Protection Ag | Pesticidally active heterocyclic derivatives with sulfur containing substituents |
| JP2023529631A (ja) | 2020-06-03 | 2023-07-11 | シンジェンタ クロップ プロテクション アクチェンゲゼルシャフト | 殺微生物性誘導体 |
| BR112022024792A2 (pt) | 2020-06-03 | 2022-12-27 | Syngenta Crop Protection Ag | Composições fungicidas |
| AU2021284956A1 (en) | 2020-06-03 | 2022-12-08 | Syngenta Crop Protection Ag | Fungicidal compositions |
| CN111567535B (zh) * | 2020-06-10 | 2024-06-21 | 青岛海利尔生物科技有限公司 | 一种含琥珀酸脱氢酶抑制剂的杀菌混合物及其应用 |
| WO2022013417A1 (en) | 2020-07-17 | 2022-01-20 | Syngenta Crop Protection Ag | Pesticidally active heterocyclic derivatives with sulfur containing substituents |
| WO2022017975A1 (en) | 2020-07-18 | 2022-01-27 | Syngenta Crop Protection Ag | Pesticidally active heterocyclic derivatives with sulfur containing substituents |
| WO2022043576A2 (en) | 2020-08-31 | 2022-03-03 | Syngenta Crop Protection Ag | Pesticidally active heterocyclic derivatives with sulfur containing substituents |
| UY39401A (es) | 2020-09-01 | 2022-03-31 | Syngenta Crop Protection Ag | Derivados de isoindolin-1-ona o 7h-pirrolo[3,4-b]piridin-5-ona activos como plaguicidas con sustituyentes que contienen azufre |
| GB202013756D0 (en) | 2020-09-02 | 2020-10-14 | Syngenta Crop Protection Ag | Plant growth regulator compounds |
| EP4208447A1 (en) | 2020-09-02 | 2023-07-12 | Syngenta Crop Protection AG | Pesticidally active heterocyclic derivatives with sulfur containing substituents |
| BR112023003939A2 (pt) | 2020-09-02 | 2023-04-11 | Syngenta Crop Protection Ag | Derivados heterocíclicos com atividade pesticida, possuindo substituintes contendo enxofre |
| UY39411A (es) | 2020-09-09 | 2022-04-29 | Syngenta Crop Protection Ag | Derivados de indazolil pirazolo[3,4-c] piridina pesticídicamente activos con sustituyentes que contienen azufre |
| GB202014840D0 (en) | 2020-09-21 | 2020-11-04 | Syngenta Crop Protection Ag | Microbiocidal compounds |
| AR124276A1 (es) | 2020-10-22 | 2023-03-15 | Syngenta Crop Protection Ag | Compuestos reguladores del crecimiento vegetal |
| WO2022101265A1 (en) | 2020-11-13 | 2022-05-19 | Syngenta Crop Protection Ag | Pesticidally active fused bicyclic heteroaromatic compounds |
| US20240122182A1 (en) | 2021-01-21 | 2024-04-18 | Syngenta Crop Protection Ag | Pesticidally active heterocyclic derivatives with sulfur containing substituents |
| CA3204213A1 (en) | 2021-01-22 | 2022-07-28 | Steven Cosky | Method for the control or suppression of phytopathogenic bacteria |
| US20240108006A1 (en) | 2021-01-23 | 2024-04-04 | Syngenta Crop Protection Ag | Pesticidally active heteroaromatic compounds |
| JP2024511476A (ja) | 2021-03-27 | 2024-03-13 | シンジェンタ クロップ プロテクション アクチェンゲゼルシャフト | 殺微生物イソニコチンアミド誘導体 |
| US20240217950A1 (en) | 2021-03-30 | 2024-07-04 | Syngenta Crop Protection Ag | Pesticidally active cyclic amine compounds |
| UY39696A (es) | 2021-03-31 | 2022-10-31 | Syngenta Crop Protection Ag | Derivados microbiocidas de quinolin/quinoxalin-benzotiazina como agentes fungicidas, en particular c |
| AR125342A1 (es) | 2021-04-16 | 2023-07-05 | Syngenta Crop Protection Ag | Compuestos de amina cíclica activos como plaguicidas |
| US20240300917A1 (en) | 2021-04-20 | 2024-09-12 | Syngenta Crop Protection Ag | Microbiocidal quinoline/quinoxaline isoquinoline derivatives |
| RS67346B1 (sr) | 2021-05-04 | 2025-11-28 | Syngenta Crop Prot Ag | Upotreba kletodima za kontrolu insekata |
| IL308616A (en) | 2021-06-01 | 2024-01-01 | Syngenta Crop Protection Ag | TETRAHYDROISOQUINOLINE MICROBIOCIDAL DERIVATIVES |
| PH12023553272A1 (en) | 2021-06-02 | 2024-04-22 | Syngenta Crop Protection Ag | Pesticidally active heterocyclic derivatives with sulfoximine containing substituents |
| BR112023025644A2 (pt) | 2021-06-09 | 2024-02-27 | Syngenta Crop Protection Ag | Compostos de diazina-amida pesticidamente ativos |
| JP2024527287A (ja) | 2021-06-24 | 2024-07-24 | シンジェンタ クロップ プロテクション アクチェンゲゼルシャフト | 殺有害生物剤としての２－［３－［１［（キナゾリン－４－イル）アミノ］エチル］ピラジン－２－イル］チアゾール－５－カルボニトリル誘導体及び類似化合物 |
| WO2023275116A1 (en) | 2021-07-02 | 2023-01-05 | Syngenta Crop Protection Ag | Use of fluazifop-p-butyl for insect control |
| WO2023006634A1 (en) | 2021-07-27 | 2023-02-02 | Syngenta Crop Protection Ag | Method for controlling diamide resistant pests & compounds therefor |
| US20240327397A1 (en) | 2021-07-29 | 2024-10-03 | Syngenta Crop Protection Ag | Pesticidally Active Fused Bicyclic Heteroaromatic Compounds |
| AU2022323303B2 (en) | 2021-08-02 | 2024-12-12 | Syngenta Crop Protection Ag | Microbiocidal pyrazole derivatives |
| WO2023012081A1 (en) | 2021-08-05 | 2023-02-09 | Syngenta Crop Protection Ag | Method for controlling diamide resistant pests & compounds therefor |
| AR126729A1 (es) | 2021-08-10 | 2023-11-08 | Syngenta Crop Protection Ag | Mezcla fungicida |
| CN117836301A (zh) | 2021-08-10 | 2024-04-05 | 先正达农作物保护股份公司 | 作为杀有害生物剂的2,2-二氟-5h-[1,3]间二氧杂环戊烯并[4,5-f]异吲哚-7-酮衍生物 |
| CN117813006A (zh) | 2021-08-19 | 2024-04-02 | 先正达农作物保护股份公司 | 用于控制二酰胺抗性有害生物的方法及其化合物 |
| PE20240951A1 (es) | 2021-10-14 | 2024-05-06 | Syngenta Crop Protection Ag | Derivados de imidazo[1,2-a]piridina |
| UY39992A (es) | 2021-10-25 | 2023-05-15 | Syngenta Crop Protection Ag | Derivados heterocíclicos activos como plaguicidas con sustituyentes que contienen azufre |
| EP4423077A1 (en) | 2021-10-27 | 2024-09-04 | Syngenta Crop Protection AG | Pesticidally active pyridazinone compounds |
| CN118019451A (zh) | 2021-10-29 | 2024-05-10 | 先正达农作物保护股份公司 | 包含咯菌腈的杀真菌组合物 |
| JP2024540114A (ja) | 2021-10-29 | 2024-10-31 | シンジェンタ クロップ プロテクション アクチェンゲゼルシャフト | 殺菌・殺カビ組成物 |
| CN118265702A (zh) | 2021-11-19 | 2024-06-28 | 先正达农作物保护股份公司 | 杀微生物的异烟酰胺衍生物 |
| WO2023094303A1 (en) | 2021-11-25 | 2023-06-01 | Syngenta Crop Protection Ag | Microbiocidal heterobiaryl amide derivatives |
| WO2023094304A1 (en) | 2021-11-25 | 2023-06-01 | Syngenta Crop Protection Ag | Microbiocidal heterobiaryl amide derivatives |
| WO2023099460A1 (en) | 2021-12-02 | 2023-06-08 | Syngenta Crop Protection Ag | Fungicidal compositions |
| US20250049033A1 (en) | 2021-12-10 | 2025-02-13 | Syngenta Crop Protection Ag | Pesticidally active pyridazinone compounds |
| WO2023110710A1 (en) | 2021-12-13 | 2023-06-22 | Syngenta Crop Protection Ag | Method for controlling diamide resistant pests & compounds therefor |
| AR127922A1 (es) | 2021-12-15 | 2024-03-13 | Syngenta Crop Protection Ag | Derivados heterocíclicos bicíclicos microbiocidas |
| EP4197333A1 (en) | 2021-12-15 | 2023-06-21 | Syngenta Crop Protection AG | Method for controlling diamide resistant pests & compounds therefor |
| JP2024546927A (ja) | 2021-12-17 | 2024-12-26 | シンジェンタ クロップ プロテクション アクチェンゲゼルシャフト | 殺微生物性ピラゾール誘導体 |
| KR20240115912A (ko) | 2021-12-17 | 2024-07-26 | 신젠타 크롭 프로텍션 아게 | 살진균 조성물 |
| WO2023111215A1 (en) | 2021-12-17 | 2023-06-22 | Syngenta Crop Protection Ag | Microbiocidal pyridine-substituted benzothiazine derivatives |
| WO2023118011A1 (en) | 2021-12-22 | 2023-06-29 | Syngenta Crop Protection Ag | Microbiocidal aza-heterobiaryl derivatives |
| WO2023118434A1 (en) | 2021-12-22 | 2023-06-29 | Globachem Nv | Pesticidally active amide compounds |
| AU2022423908A1 (en) | 2021-12-22 | 2024-06-20 | Syngenta Crop Protection Ag | Fungicidal compositions |
| WO2023139166A1 (en) | 2022-01-19 | 2023-07-27 | Syngenta Crop Protection Ag | Methods for controlling plant pathogens |
| WO2023148206A1 (en) | 2022-02-02 | 2023-08-10 | Syngenta Crop Protection Ag | Microbiocidal n-amide derivatives |
| UY40138A (es) | 2022-02-07 | 2023-08-31 | Syngenta Crop Protection Ag | Derivados de pirazolo[3,4-c]piridin-5-il]-2-quinoxalina o 2-quinolina activos como pesticidas con su |
| UY40139A (es) | 2022-02-07 | 2023-08-31 | Syngenta Crop Protection Ag | Derivados de imidazo[1,2-a]piridin-2-il]-1-pirazolo[3,4-c]piridina activos como pesticidas con susti |
| WO2023166067A1 (en) | 2022-03-02 | 2023-09-07 | Syngenta Crop Protection Ag | Microbiocidal pyridazinone amide derivatives |
| WO2023187191A1 (en) | 2022-04-01 | 2023-10-05 | Syngenta Crop Protection Ag | Pesticidally active heterocyclic derivatives with sulfur containing substituents |
| AR129158A1 (es) | 2022-04-29 | 2024-07-24 | Syngenta Crop Protection Ag | Composiciones fungicidas de metarilpicoxamid |
| AR129265A1 (es) | 2022-05-12 | 2024-08-07 | Syngenta Crop Protection Ag | Compuestos de alcoxi-heteroaril-carboxamida o tioamida |
| JP2025520650A (ja) | 2022-06-21 | 2025-07-03 | シンジェンタ クロップ プロテクション アクチェンゲゼルシャフト | 殺有害生物的に活性な縮合二環式芳香族複素環式化合物 |
| AR129535A1 (es) | 2022-06-21 | 2024-09-04 | Syngenta Crop Protection Ag | Derivados de carboxamida heterocíclicos bicíclicos microbiocidas |
| EP4551017A1 (en) | 2022-07-07 | 2025-05-14 | Syngenta Crop Protection AG | Precision application devices and compositions |
| CN119677724A (zh) | 2022-07-21 | 2025-03-21 | 先正达农作物保护股份公司 | 1,2,4-噁二唑杀真菌剂的结晶形式 |
| JP2025524004A (ja) | 2022-07-22 | 2025-07-25 | シンジェンタ クロップ プロテクション アクチェンゲゼルシャフト | 複素環アミド誘導体の固体形態 |
| WO2024022910A1 (en) | 2022-07-26 | 2024-02-01 | Syngenta Crop Protection Ag | 1-[1-[2-(pyrimidin-4-yl)-1,2,4-triazol-3-yl]ethyl]-3-[2,4-dichloro-5-phenyl]urea derivatives and similar compounds as pesticides |
| WO2024033374A1 (en) | 2022-08-11 | 2024-02-15 | Syngenta Crop Protection Ag | Novel arylcarboxamide or arylthioamide compounds |
| TW202412626A (zh) | 2022-08-16 | 2024-04-01 | 瑞士商先正達農作物保護股份公司 | 新用途 |
| WO2024056732A1 (en) | 2022-09-16 | 2024-03-21 | Syngenta Crop Protection Ag | Pesticidally active cyclic amine compounds |
| GB202214203D0 (en) | 2022-09-28 | 2022-11-09 | Syngenta Crop Protection Ag | Fungicidal compositions |
| WO2024068656A1 (en) | 2022-09-28 | 2024-04-04 | Syngenta Crop Protection Ag | Fungicidal compositions |
| AR130567A1 (es) | 2022-09-28 | 2024-12-18 | Syngenta Crop Protection Ag | Composiciones fungicidas |
| TW202430514A (zh) | 2022-09-30 | 2024-08-01 | 瑞士商先正達農作物保護股份公司 | 殺微生物之吡唑衍生物 |
| TW202430031A (zh) | 2022-09-30 | 2024-08-01 | 瑞士商先正達農作物保護股份公司 | 殺微生物之吡唑衍生物 |
| EP4608813A1 (en) | 2022-10-25 | 2025-09-03 | Syngenta Crop Protection AG | Pesticidally active heterocyclic derivatives with sulfur containing substituents |
| WO2024089216A1 (en) | 2022-10-27 | 2024-05-02 | Syngenta Crop Protection Ag | Novel sulfur-containing heteroaryl carboxamide compounds |
| CN120476119A (zh) | 2022-10-27 | 2025-08-12 | 先正达农作物保护股份公司 | 杀微生物的杂双环二氢噁二嗪衍生物 |
| WO2024094575A1 (en) | 2022-10-31 | 2024-05-10 | Syngenta Crop Protection Ag | Pesticidally active heterocyclic derivatives with sulfur containing substituents |
| WO2024100069A1 (en) | 2022-11-08 | 2024-05-16 | Syngenta Crop Protection Ag | Microbiocidal pyridine derivatives |
| TW202434557A (zh) | 2022-11-09 | 2024-09-01 | 瑞士商先正達農作物保護股份公司 | 殺微生物之吡唑衍生物 |
| TW202434579A (zh) | 2022-11-16 | 2024-09-01 | 瑞士商先正達農作物保護股份公司 | 殺微生物的四氫異喹啉衍生物 |
| WO2024110554A1 (en) | 2022-11-23 | 2024-05-30 | Syngenta Crop Protection Ag | N-[(1 -[2-[6-(pyridazin-3-yl]-1,2,4-triazol-3-yl]ethyl]-quinazolin-4-amine and n-[1-[3-(6-(pyridazin-3-yl)pyrazin-2-yl]ethyl]-8-quinazolin-4-amine derivatives as pesticides |
| WO2024110215A1 (en) | 2022-11-24 | 2024-05-30 | Syngenta Crop Protection Ag | Pesticidally active cyclic amine compounds |
| AR131180A1 (es) | 2022-11-29 | 2025-02-26 | Syngenta Crop Protection Ag | Derivados microbicidas de tetrahidroisoquinolina |
| TW202439972A (zh) | 2022-11-30 | 2024-10-16 | 瑞士商先正達農作物保護股份公司 | 殺真菌組成物 |
| CN120282962A (zh) | 2022-11-30 | 2025-07-08 | 先正达农作物保护股份公司 | 杀微生物的四氢异喹啉衍生物 |
| WO2024126388A1 (en) | 2022-12-12 | 2024-06-20 | Syngenta Crop Protection Ag | Pesticidally active heterocyclic derivatives with sulfur containing substituents |
| TW202440570A (zh) | 2022-12-14 | 2024-10-16 | 瑞士商先正達農作物保護股份公司 | 咪唑并[1,2-a]吡啶衍生物 |
| CN120476107A (zh) | 2022-12-15 | 2025-08-12 | 先正达农作物保护股份公司 | 可用作杀有害生物剂的新型的二环-甲酰胺化合物 |
| AU2023393591A1 (en) | 2022-12-16 | 2025-06-05 | Syngenta Crop Protection Ag | Benzimidazole derivatives |
| WO2024132895A1 (en) | 2022-12-19 | 2024-06-27 | Syngenta Crop Protection Ag | Microbiocidal dihydrooxadiazinyl pyridazinone compounds |
| EP4638425A1 (en) | 2022-12-19 | 2025-10-29 | Syngenta Crop Protection AG | Microbiocidal pyridazine dihydrooxadiazine derivatives |
| WO2024133426A1 (en) | 2022-12-21 | 2024-06-27 | Syngenta Crop Protection Ag | Method for controlling diamide resistant pests and compounds therefor |
| WO2024133551A1 (en) | 2022-12-21 | 2024-06-27 | Syngenta Crop Protection Ag | Pesticidally active pyridazine compounds |
| AR131541A1 (es) | 2023-01-07 | 2025-04-09 | Syngenta Crop Protection Ag | Compuestos de carboxamida novedosos |
| WO2024156664A1 (en) | 2023-01-23 | 2024-08-02 | Syngenta Crop Protection Ag | Pesticidally active heterocyclic derivatives with sulfur containing substituents |
| AR131667A1 (es) | 2023-01-27 | 2025-04-16 | Syngenta Crop Protection Ag | Derivados de pirazol microbiocidas |
| AR131665A1 (es) | 2023-02-01 | 2025-04-16 | Syngenta Crop Protection Ag | Composiciones fungicidas |
| WO2024170339A1 (en) | 2023-02-13 | 2024-08-22 | Syngenta Crop Protection Ag | Pesticidally active bicyclic compounds |
| WO2024170484A1 (en) | 2023-02-13 | 2024-08-22 | Globachem Nv | Pesticidally active amide compounds |
| WO2024170365A1 (en) | 2023-02-14 | 2024-08-22 | Syngenta Crop Protection Ag | Composition comprising cyprodinil and lactose-based filler |
| WO2025201636A1 (en) | 2023-03-31 | 2025-10-02 | Syngenta Crop Protection Ag | Pesticidally-active 2,2-dihalocyclopropyl compounds |
| WO2024213653A1 (en) | 2023-04-13 | 2024-10-17 | Syngenta Crop Protection Ag | Imidazo[1,2-a]pyridine derivatives |
| WO2024213651A1 (en) | 2023-04-13 | 2024-10-17 | Syngenta Crop Protection Ag | Imidazo[1,2-a]pyridine derivatives |
| AR132354A1 (es) | 2023-04-13 | 2025-06-18 | Syngenta Crop Protection Ag | Derivados de pirazolo[1,5-a]piridina |
| CN120957990A (zh) | 2023-04-13 | 2025-11-14 | 先正达农作物保护股份公司 | 咪唑并[1,2-a]吡啶衍生物 |
| AR132352A1 (es) | 2023-04-13 | 2025-06-18 | Syngenta Crop Protection Ag | Derivados de imidazo[1,2-a]pirazina |
| AR132358A1 (es) | 2023-04-13 | 2025-06-18 | Syngenta Crop Protection Ag | Derivados bicíclicos de imidazo |
| TW202446263A (zh) | 2023-04-13 | 2024-12-01 | 瑞士商先正達農作物保護股份公司 | 殺真菌組成物 |
| AR132351A1 (es) | 2023-04-13 | 2025-06-18 | Syngenta Crop Protection Ag | Derivados de imidazo[1,2-a]pirazina |
| AR132353A1 (es) | 2023-04-13 | 2025-06-18 | Syngenta Crop Protection Ag | Derivados de pirazolo[1,5-a]piridina |
| WO2025214612A1 (en) | 2023-04-14 | 2025-10-16 | Syngenta Crop Protection Ag | Pesticidally-active 2,2-dihalocyclopropyl compounds |
| WO2024217995A1 (en) | 2023-04-20 | 2024-10-24 | Syngenta Crop Protection Ag | Pesticidally active dihydropyridinone derivatives |
| WO2024256433A1 (en) | 2023-06-14 | 2024-12-19 | Syngenta Crop Protection Ag | Fungicidal compositions |
| WO2024256438A1 (en) | 2023-06-14 | 2024-12-19 | Syngenta Crop Protection Ag | Fungicidal compositions |
| WO2025021537A1 (en) | 2023-07-21 | 2025-01-30 | Syngenta Crop Protection Ag | Benzimidazole derivatives |
| WO2025022008A1 (en) | 2023-07-27 | 2025-01-30 | Syngenta Crop Protection Ag | Pesticidally active quinazoline compounds |
| WO2025022007A1 (en) | 2023-07-27 | 2025-01-30 | Syngenta Crop Protection Ag | Pesticidally active quinazoline compounds |
| WO2025032129A1 (en) | 2023-08-08 | 2025-02-13 | Syngenta Crop Protection Ag | Novel aminoindane and aminotetraline compounds |
| WO2025045835A1 (en) | 2023-08-30 | 2025-03-06 | Syngenta Crop Protection Ag | Pesticidally active oxoindole compounds |
| WO2025045838A2 (en) | 2023-08-31 | 2025-03-06 | Syngenta Crop Protection Ag | Pesticidally active benzisothiazole compounds |
| WO2025045837A1 (en) | 2023-08-31 | 2025-03-06 | Syngenta Crop Protection Ag | Pesticidally active indazole compounds |
| TW202513532A (zh) | 2023-09-15 | 2025-04-01 | 瑞士商先正達農作物保護股份公司 | 用於製備鏡像異構物富集的脂肪族胺之方法 |
| WO2025078263A1 (en) | 2023-10-11 | 2025-04-17 | Syngenta Crop Protection Ag | Microbiocidal pyridyl pyrazole derivatives |
| WO2025087761A1 (en) | 2023-10-27 | 2025-05-01 | Syngenta Crop Protection Ag | Pesticidally active cyclic amine compounds |
| CN119912444A (zh) * | 2023-10-31 | 2025-05-02 | 青岛清原化合物有限公司 | 烟酸酯类化合物及其应用 |
| WO2025104032A1 (en) | 2023-11-14 | 2025-05-22 | Syngenta Crop Protection Ag | Novel carboxamide compounds |
| WO2025104152A1 (en) | 2023-11-15 | 2025-05-22 | Syngenta Crop Protection Ag | Microbiocidal tetrahydroisoquinoline derivatives |
| WO2025109114A1 (en) | 2023-11-24 | 2025-05-30 | Syngenta Crop Protection Ag | Novel carboxamide compounds |
| WO2025114167A1 (en) | 2023-11-28 | 2025-06-05 | Syngenta Crop Protection Ag | Microbiocidal pyrazole derivatives |
| WO2025120070A1 (en) | 2023-12-08 | 2025-06-12 | Syngenta Crop Protection Ag | Polymorphs of a methoxyacrylate derivative |
| WO2025132349A1 (en) | 2023-12-19 | 2025-06-26 | Syngenta Crop Protection Ag | Pesticidally active quinazoline compounds |
| WO2025132754A1 (en) | 2023-12-21 | 2025-06-26 | Syngenta Crop Protection Ag | Pesticidally active quinazoline compounds |
| WO2025132758A1 (en) | 2023-12-21 | 2025-06-26 | Syngenta Crop Protection Ag | Pesticidally active quinazoline compounds |
| WO2025149637A1 (en) | 2024-01-12 | 2025-07-17 | Syngenta Crop Protection Ag | Novel carboxamide compounds |
| WO2025149629A1 (en) | 2024-01-12 | 2025-07-17 | Syngenta Crop Protection Ag | Novel carboxamide compounds |
| WO2025163143A1 (en) | 2024-02-02 | 2025-08-07 | Syngenta Crop Protection Ag | Microbiocidal pyrazole derivatives |
| WO2025172368A1 (en) | 2024-02-13 | 2025-08-21 | Syngenta Crop Protection Ag | (5-isoxazol-3-yl)-[4-(pyrazol-4-yl)-3,4-dihydro-1h-isoquinolin-2-yl]methanone derivatives for use as fungicides |
| WO2025172374A1 (en) | 2024-02-13 | 2025-08-21 | Syngenta Crop Protection Ag | Microbiocidal pyrazole derivatives |
| WO2025191053A1 (en) | 2024-03-14 | 2025-09-18 | Syngenta Crop Protection Ag | Microbiocidal pyrazole derivatives |
| WO2025202499A1 (en) | 2024-03-28 | 2025-10-02 | Syngenta Crop Protection Ag | Fungicidal compositions |
| WO2025202482A1 (en) | 2024-03-28 | 2025-10-02 | Syngenta Crop Protection Ag | Fungicidal compositions |
| WO2025210096A1 (en) | 2024-04-03 | 2025-10-09 | Syngenta Crop Protection Ag | Fungicidal compositions |
| WO2025210095A1 (en) | 2024-04-03 | 2025-10-09 | Syngenta Crop Protection Ag | Microbiocidal tetrahydroisoquinoline compounds |
| WO2025210149A1 (en) | 2024-04-04 | 2025-10-09 | Syngenta Crop Protection Ag | Fungicidal composition |
| WO2025233384A1 (en) | 2024-05-08 | 2025-11-13 | Syngenta Crop Protection Ag | Microbiocidal pyrazole compounds |
| WO2025238048A1 (en) | 2024-05-15 | 2025-11-20 | Syngenta Crop Protection Ag | Fungicidal compositions |
| WO2025247783A1 (en) | 2024-05-29 | 2025-12-04 | Syngenta Crop Protection Ag | Pesticidally active dihydro-benzoxazinone compounds |
| WO2025248032A1 (en) | 2024-05-31 | 2025-12-04 | Syngenta Crop Protection Ag | Pesticidally active indazole compounds |
Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2037487C1 (ru) * | 1987-10-15 | 1995-06-19 | Империал Кемикал Индастриз ПЛС | Производные акриловой кислоты и их стереоизомеры, обладающие фунгицидной активностью |
| JPH09249648A (ja) * | 1996-03-18 | 1997-09-22 | Dainippon Ink & Chem Inc | ２，６−ジクロロイソニコチン酸フェノキシアルキルアミド誘導体及び農薬 |
| JPH1072440A (ja) * | 1996-08-30 | 1998-03-17 | Dainippon Ink & Chem Inc | ２，６−ジクロロイソニコチン酸誘導体及び植物病害防除剤 |
| WO1998033772A1 (en) * | 1997-02-03 | 1998-08-06 | Dow Agrosciences Llc | 2-methoxyimino-2-(pyridinyloxymethyl)phenyl acetamides with carboxylic acid derivatives on the pyridine ring as fungicides |
| WO2005068430A1 (ja) * | 2004-01-13 | 2005-07-28 | Kureha Corporation | ２，６−ジクロロイソニコチン酸ピリジルメチル誘導体、その製造方法および農園芸用病害防除剤 |
| JP2010083861A (ja) * | 2008-02-27 | 2010-04-15 | Sumitomo Chemical Co Ltd | 植物病原菌による植物病害を防除又は予防するための農業用組成物 |
| US20100168175A1 (en) * | 2008-12-18 | 2010-07-01 | Bayer Cropscience Ag | Atpenins |
Family Cites Families (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE4319887A1 (de) | 1993-06-16 | 1994-12-22 | Hoechst Schering Agrevo Gmbh | Arylacetamide, Verfahren zu ihrer Herstellung, sie enthaltende Mittel und ihre Verwendung als Fungizide |
| DE59401924D1 (de) | 1993-11-02 | 1997-04-10 | Hoechst Ag | Substituierte heterocyclische Carbonsäureamide, ihre Herstellung und ihre Verwendung als Arzneimittel |
| US5877177A (en) | 1997-06-17 | 1999-03-02 | Schering Corporation | Carboxy piperidylacetamide tricyclic compounds useful for inhibition of G-protein function and for treatment of proliferative diseases |
| PT1114030E (pt) | 1998-09-15 | 2005-09-30 | Syngenta Participations Ag | Piridina cetonas uteis como herbicidas |
| JP2004149413A (ja) | 2000-06-30 | 2004-05-27 | Agro Kanesho Co Ltd | 有害生物の防除に有効なヒドラゾン誘導体又はその塩 |
| JP2004051628A (ja) | 2002-05-28 | 2004-02-19 | Ishihara Sangyo Kaisha Ltd | ピリジン系化合物又はその塩、それらの製造方法及びそれらを含有する除草剤 |
| PL372418A1 (en) | 2002-05-30 | 2005-07-25 | Solvay Pharmaceuticals B.V. | 1,3,5-triazine derivatives as ligands for human adenosine-a3 receptors |
| US7307079B2 (en) | 2002-05-30 | 2007-12-11 | Solvay Pharmaceuticals, B.V. | 1,3,5-Triazine derivatives as ligands for human adenosine-A3 receptors |
| US20060063820A1 (en) | 2002-12-23 | 2006-03-23 | Peter Renold | 2,6-dihalo-4-(3,3-dichloro-allyloxy)-benzylalcohole derivatives having insecticidal and acaricidal properties |
| US20080247964A1 (en) | 2006-05-08 | 2008-10-09 | Yuelian Xu | Substituted azaspiro derivatives |
| WO2008082490A2 (en) | 2006-12-20 | 2008-07-10 | Schering Corporation | Novel jnk inhibitors |
| NZ591366A (en) | 2008-09-11 | 2012-05-25 | Pfizer | Heteroaryls amide derivatives and their use as glucokinase activators |
| US20110190267A1 (en) | 2010-01-05 | 2011-08-04 | Shire Pharmaceuticals, Inc. | Prodrugs of opioids and uses thereof |
-
2013
- 2013-04-02 RU RU2015103515/04A patent/RU2599725C2/ru active
- 2013-04-02 BR BR112014032873-0A patent/BR112014032873B1/pt active IP Right Grant
- 2013-04-02 US US14/412,130 patent/US9096528B2/en active Active
- 2013-04-02 AU AU2013284775A patent/AU2013284775B2/en active Active
- 2013-04-02 CA CA2877235A patent/CA2877235C/en active Active
- 2013-04-02 JP JP2014523622A patent/JP6114958B2/ja active Active
- 2013-04-02 ES ES13812665.1T patent/ES2665561T3/es active Active
- 2013-04-02 WO PCT/JP2013/060061 patent/WO2014006945A1/ja not_active Ceased
- 2013-04-02 IN IN10806DEN2014 patent/IN2014DN10806A/en unknown
- 2013-04-02 CN CN201380035233.9A patent/CN104520273B/zh active Active
- 2013-04-02 KR KR1020157002648A patent/KR101629767B1/ko active Active
- 2013-04-02 MA MA37825A patent/MA37825B1/fr unknown
- 2013-04-02 HU HUE13812665A patent/HUE037765T2/hu unknown
- 2013-04-02 EP EP13812665.1A patent/EP2871180B1/en active Active
- 2013-04-02 UA UAA201500284A patent/UA111542C2/uk unknown
- 2013-04-02 PT PT138126651T patent/PT2871180T/pt unknown
- 2013-04-02 PL PL13812665T patent/PL2871180T3/pl unknown
-
2014
- 2014-12-31 CL CL2014003643A patent/CL2014003643A1/es unknown
-
2015
- 2015-01-23 CO CO15013754A patent/CO7240428A2/es unknown
- 2015-02-02 ZA ZA2015/00742A patent/ZA201500742B/en unknown
Patent Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2037487C1 (ru) * | 1987-10-15 | 1995-06-19 | Империал Кемикал Индастриз ПЛС | Производные акриловой кислоты и их стереоизомеры, обладающие фунгицидной активностью |
| JPH09249648A (ja) * | 1996-03-18 | 1997-09-22 | Dainippon Ink & Chem Inc | ２，６−ジクロロイソニコチン酸フェノキシアルキルアミド誘導体及び農薬 |
| JPH1072440A (ja) * | 1996-08-30 | 1998-03-17 | Dainippon Ink & Chem Inc | ２，６−ジクロロイソニコチン酸誘導体及び植物病害防除剤 |
| WO1998033772A1 (en) * | 1997-02-03 | 1998-08-06 | Dow Agrosciences Llc | 2-methoxyimino-2-(pyridinyloxymethyl)phenyl acetamides with carboxylic acid derivatives on the pyridine ring as fungicides |
| WO2005068430A1 (ja) * | 2004-01-13 | 2005-07-28 | Kureha Corporation | ２，６−ジクロロイソニコチン酸ピリジルメチル誘導体、その製造方法および農園芸用病害防除剤 |
| JP2010083861A (ja) * | 2008-02-27 | 2010-04-15 | Sumitomo Chemical Co Ltd | 植物病原菌による植物病害を防除又は予防するための農業用組成物 |
| US20100168175A1 (en) * | 2008-12-18 | 2010-07-01 | Bayer Cropscience Ag | Atpenins |
Also Published As
| Publication number | Publication date |
|---|---|
| US20150175551A1 (en) | 2015-06-25 |
| KR101629767B1 (ko) | 2016-06-13 |
| BR112014032873B1 (pt) | 2019-02-12 |
| PT2871180T (pt) | 2018-05-08 |
| HUE037765T2 (hu) | 2018-09-28 |
| CN104520273A (zh) | 2015-04-15 |
| MA37825B1 (fr) | 2016-06-30 |
| JPWO2014006945A1 (ja) | 2016-06-02 |
| BR112014032873A2 (pt) | 2017-06-27 |
| RU2015103515A (ru) | 2016-08-20 |
| AU2013284775A1 (en) | 2015-01-29 |
| CA2877235C (en) | 2016-09-20 |
| IN2014DN10806A (enExample) | 2015-09-04 |
| CL2014003643A1 (es) | 2015-07-31 |
| CA2877235A1 (en) | 2014-01-09 |
| UA111542C2 (uk) | 2016-05-10 |
| US9096528B2 (en) | 2015-08-04 |
| JP6114958B2 (ja) | 2017-04-19 |
| EP2871180B1 (en) | 2018-03-21 |
| WO2014006945A1 (ja) | 2014-01-09 |
| ZA201500742B (en) | 2016-09-28 |
| KR20150042781A (ko) | 2015-04-21 |
| CN104520273B (zh) | 2016-08-24 |
| PL2871180T3 (pl) | 2018-08-31 |
| CO7240428A2 (es) | 2015-04-17 |
| ES2665561T3 (es) | 2018-04-26 |
| EP2871180A1 (en) | 2015-05-13 |
| AU2013284775B2 (en) | 2015-09-17 |
| EP2871180A4 (en) | 2016-02-24 |
| MA20150409A1 (fr) | 2015-11-30 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| RU2599725C2 (ru) | Производное соединение сложного эфира 2-аминоникотиновой кислоты и бактерицид, содержащий то же самое в качестве активного ингредиента | |
| RU2573769C2 (ru) | Композиция для борьбы с заболеванием растений и способ борьбы с заболеванием растений | |
| JP6286693B2 (ja) | ６−置換ニコチン酸エステル誘導体およびこれを有効成分とする殺菌剤 | |
| EP3025586B1 (en) | Plant disease control composition and its use | |
| EP3025585A1 (en) | Plant disease control composition and application for same | |
| JP2015089883A (ja) | ２−アミノニコチン酸ベンジルエステル誘導体およびこれを有効成分とする殺菌剤 | |
| JP2009078991A (ja) | チオフェンカルボン酸誘導体およびその製造方法、並びに殺菌剤 | |
| JP3824421B2 (ja) | 植物病害防除剤組成物 | |
| JP6212773B2 (ja) | ２−アミノニコチン酸ベンジル誘導体およびこれを有効成分とする殺菌剤 | |
| JP3963569B2 (ja) | 植物病害防除剤組成物 | |
| WO2011128989A1 (ja) | ピラジン-2-カルボキサミド誘導体及びこれを有効成分とする殺菌剤 | |
| JPWO2016114164A1 (ja) | カルバメート化合物及びその用途 | |
| WO2016114161A1 (ja) | カルバメート化合物及びその用途 | |
| WO2016114162A1 (ja) | カルバメート化合物及びその用途 | |
| JP2012201640A (ja) | ベンゼン−２−カルボキサミド誘導体およびこれを有効成分とする殺菌剤 | |
| WO2016114163A1 (ja) | カルバメート化合物及びその用途 | |
| WO2016114165A1 (ja) | カルバメート化合物及びその用途 | |
| JP2019031442A (ja) | キノキサリルイソキノリン化合物 | |
| JP6331084B2 (ja) | ２−ベンジルアミノニコチン酸エステル誘導体およびこれを有効成分とする殺菌剤 | |
| JP6331075B2 (ja) | ３−アミノ−１ｈ−ピラゾール−４−カルボン酸ベンジルエステル誘導体およびこれを有効成分とする殺菌剤 | |
| WO2015190601A1 (ja) | ２－アシルアミノニコチン酸エステル誘導体およびこれを有効成分とする殺菌剤 | |
| JP4545713B2 (ja) | 植物病害防除剤組成物 |