BE568137A - - Google Patents
Info
- Publication number
- BE568137A BE568137A BE568137DA BE568137A BE 568137 A BE568137 A BE 568137A BE 568137D A BE568137D A BE 568137DA BE 568137 A BE568137 A BE 568137A
- Authority
- BE
- Belgium
- Prior art keywords
- sep
- group
- active compound
- bithienyl
- substituents
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 claims description 24
- 241000244206 Nematoda Species 0.000 claims description 16
- 230000000875 corresponding Effects 0.000 claims description 10
- 229910052739 hydrogen Inorganic materials 0.000 claims description 10
- 239000001257 hydrogen Substances 0.000 claims description 10
- 125000001424 substituent group Chemical group 0.000 claims description 10
- 239000000203 mixture Substances 0.000 claims description 8
- 239000002270 dispersing agent Substances 0.000 claims description 6
- 239000000463 material Substances 0.000 claims description 6
- 125000002252 acyl group Chemical group 0.000 claims description 5
- 125000001931 aliphatic group Chemical group 0.000 claims description 5
- 150000002431 hydrogen Chemical class 0.000 claims description 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 5
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 5
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 5
- YTPLMLYBLZKORZ-UHFFFAOYSA-N thiophene Chemical group C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 claims description 5
- 125000004417 unsaturated alkyl group Chemical group 0.000 claims description 5
- 125000005843 halogen group Chemical group 0.000 claims description 4
- 238000007792 addition Methods 0.000 claims description 3
- 239000000853 adhesive Substances 0.000 claims description 3
- 230000001070 adhesive Effects 0.000 claims description 3
- 125000000217 alkyl group Chemical group 0.000 claims description 3
- 239000006185 dispersion Substances 0.000 claims description 3
- 239000012442 inert solvent Substances 0.000 claims description 3
- 239000007788 liquid Substances 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 3
- 238000000034 method Methods 0.000 claims description 3
- 239000004094 surface-active agent Substances 0.000 claims description 3
- WGSCFRDYMPBHBJ-UHFFFAOYSA-N 2-nitro-5-thiophen-2-ylthiophene Chemical group S1C([N+](=O)[O-])=CC=C1C1=CC=CS1 WGSCFRDYMPBHBJ-UHFFFAOYSA-N 0.000 claims description 2
- FJDUBXOCPMPNNX-UHFFFAOYSA-N 2-phenyl-5-thiophen-2-ylthiophene Chemical group C1=CSC(C=2SC(=CC=2)C=2C=CC=CC=2)=C1 FJDUBXOCPMPNNX-UHFFFAOYSA-N 0.000 claims description 2
- 239000000969 carrier Substances 0.000 claims description 2
- 239000000725 suspension Substances 0.000 claims 2
- MRWPBEHIJTUNGC-UHFFFAOYSA-N 1-(5-thiophen-2-ylthiophen-2-yl)propan-1-one Chemical group S1C(C(=O)CC)=CC=C1C1=CC=CS1 MRWPBEHIJTUNGC-UHFFFAOYSA-N 0.000 claims 1
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 claims 1
- 230000000249 desinfective Effects 0.000 claims 1
- 239000000843 powder Substances 0.000 claims 1
- 229920001098 polystyrene-block-poly(ethylene/propylene) Polymers 0.000 description 315
- 241000196324 Embryophyta Species 0.000 description 18
- 239000000243 solution Substances 0.000 description 16
- 239000000126 substance Substances 0.000 description 10
- 241000380490 Anguina Species 0.000 description 8
- 238000010790 dilution Methods 0.000 description 8
- 241000399934 Ditylenchus Species 0.000 description 7
- 239000003995 emulsifying agent Substances 0.000 description 7
- 241001480224 Heterodera Species 0.000 description 6
- 239000007864 aqueous solution Substances 0.000 description 6
- RYGMFSIKBFXOCR-UHFFFAOYSA-N copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 5
- 238000010438 heat treatment Methods 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- CSCPPACGZOOCGX-UHFFFAOYSA-N acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- ROIMNSWDOJCBFR-UHFFFAOYSA-N 2-iodothiophene Chemical compound IC1=CC=CS1 ROIMNSWDOJCBFR-UHFFFAOYSA-N 0.000 description 3
- 240000005158 Phaseolus vulgaris Species 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- ORTQZVOHEJQUHG-UHFFFAOYSA-L Copper(II) chloride Chemical compound Cl[Cu]Cl ORTQZVOHEJQUHG-UHFFFAOYSA-L 0.000 description 2
- 241001442497 Globodera rostochiensis Species 0.000 description 2
- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 2
- 238000004587 chromatography analysis Methods 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 238000000605 extraction Methods 0.000 description 2
- 229910052736 halogen Inorganic materials 0.000 description 2
- 238000003898 horticulture Methods 0.000 description 2
- OKKJLVBELUTLKV-UHFFFAOYSA-N methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 2
- CSNNHWWHGAXBCP-UHFFFAOYSA-L mgso4 Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
- MYMOFIZGZYHOMD-UHFFFAOYSA-N oxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 125000001544 thienyl group Chemical group 0.000 description 2
- 238000009834 vaporization Methods 0.000 description 2
- OHZAHWOAMVVGEL-UHFFFAOYSA-N 2,2'-bithiophene Chemical group C1=CSC(C=2SC=CC=2)=C1 OHZAHWOAMVVGEL-UHFFFAOYSA-N 0.000 description 1
- NLLYFHBKYPUMQM-UHFFFAOYSA-N 2-chloro-5-(5-chlorothiophen-2-yl)thiophene Chemical group S1C(Cl)=CC=C1C1=CC=C(Cl)S1 NLLYFHBKYPUMQM-UHFFFAOYSA-N 0.000 description 1
- NAZNQEXKAPLVKC-UHFFFAOYSA-N 2-iodo-5-methylthiophene Chemical compound CC1=CC=C(I)S1 NAZNQEXKAPLVKC-UHFFFAOYSA-N 0.000 description 1
- 241000399940 Anguina tritici Species 0.000 description 1
- 241000219195 Arabidopsis thaliana Species 0.000 description 1
- 240000005528 Arctium lappa Species 0.000 description 1
- 235000007319 Avena orientalis Nutrition 0.000 description 1
- 244000075850 Avena orientalis Species 0.000 description 1
- 235000016068 Berberis vulgaris Nutrition 0.000 description 1
- 241000335053 Beta vulgaris Species 0.000 description 1
- 235000011305 Capsella bursa pastoris Nutrition 0.000 description 1
- 240000008867 Capsella bursa-pastoris Species 0.000 description 1
- 244000192528 Chrysanthemum parthenium Species 0.000 description 1
- 241000207892 Convolvulus Species 0.000 description 1
- 241000399949 Ditylenchus dipsaci Species 0.000 description 1
- 210000001161 Embryo, Mammalian Anatomy 0.000 description 1
- 241001540513 Hoplolaimus Species 0.000 description 1
- 241000282619 Hylobates lar Species 0.000 description 1
- 241000209082 Lolium Species 0.000 description 1
- 235000007688 Lycopersicon esculentum Nutrition 0.000 description 1
- 241001143352 Meloidogyne Species 0.000 description 1
- 229920001213 Polysorbate 20 Polymers 0.000 description 1
- 241000193943 Pratylenchus Species 0.000 description 1
- HBECXKQAIQCROH-UHFFFAOYSA-N S1C(C)=CC=C1C1=C(C=2SC=CC=2)C=CS1 Chemical group S1C(C)=CC=C1C1=C(C=2SC=CC=2)C=CS1 HBECXKQAIQCROH-UHFFFAOYSA-N 0.000 description 1
- 240000003768 Solanum lycopersicum Species 0.000 description 1
- 240000006694 Stellaria media Species 0.000 description 1
- 235000012308 Tagetes Nutrition 0.000 description 1
- 241000736851 Tagetes Species 0.000 description 1
- 240000008529 Triticum aestivum Species 0.000 description 1
- 241001540447 Tylenchus Species 0.000 description 1
- 241000219422 Urtica Species 0.000 description 1
- GSHPYJFNTAMRJF-UHFFFAOYSA-M [Br-].[Mg+]C1=CC=CS1 Chemical compound [Br-].[Mg+]C1=CC=CS1 GSHPYJFNTAMRJF-UHFFFAOYSA-M 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 230000001058 adult Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000005712 crystallization Effects 0.000 description 1
- 229960003280 cupric chloride Drugs 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 238000004508 fractional distillation Methods 0.000 description 1
- 238000000260 fractional sublimation Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 235000021332 kidney beans Nutrition 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 230000001069 nematicidal Effects 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 230000000885 phytotoxic Effects 0.000 description 1
- 239000000256 polyoxyethylene sorbitan monolaurate Substances 0.000 description 1
- 235000010486 polyoxyethylene sorbitan monolaurate Nutrition 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000007127 saponification reaction Methods 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 150000003577 thiophenes Chemical class 0.000 description 1
- 235000021307 wheat Nutrition 0.000 description 1
Classifications
-
- 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
- A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
- A01N43/04—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
- A01N43/06—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings
- A01N43/10—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings with sulfur as the ring hetero atom
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Publications (1)
Publication Number | Publication Date |
---|---|
BE568137A true BE568137A (ja) |
Family
ID=187592
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
BE568137D BE568137A (ja) |
Country Status (1)
Country | Link |
---|---|
BE (1) | BE568137A (ja) |
-
0
- BE BE568137D patent/BE568137A/fr unknown
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CH643546A5 (fr) | Procede pour la preparation de derives d'hydantoine. | |
FR2899586A1 (fr) | Dimeres de derives d'artemisinine, leur preparation et leur application en therapeutique | |
CA2160961C (fr) | Nouveaux composes amides tricycliques, leur procede de preparation et les compositions pharmaceutiques qui les contiennent | |
EP0919541B1 (fr) | Nouveaux composés naphtaléniques, leur procédé de préparation et les compositions pharmaceutiques qui les contiennent | |
EP0721938B1 (fr) | Nouveaux composés (hétéro)cycliques alkylés, leur procédé de préparation et les compositions pharmaceutiques qui les contiennent | |
US3050442A (en) | Method of destroying nematodes with polythienyl compounds | |
EP0239436B1 (fr) | Nouveau dérivé tricyclique dénommé acide (chloro-3 méthyl-6 dioxo-5,5 dihydro-6, 11 dibenzo (c,f) thiazépine (1,2) yl-11 amino) -5 pentanoique, son procédé de préparation et les compositions pharmaceutiques qui le contiennent | |
EP0873993B1 (fr) | Nouveaux composés hétérocycliques, leur procédé de préparation et les compositions pharmaceutiques qui les contiennent | |
BE568137A (ja) | ||
CA2256247C (fr) | Nouveaux composes heterocycliques, leur procede de praparation et les compositions pharmaceutiques qui les contiennent | |
BE897354A (fr) | Derives de 1-phenoxy (phenylthio)-4-arylal-kynyloxy-benzene pourvus d'une activite acaricide et d'une activite hormonale juvenile | |
CA2055325A1 (fr) | Nouveaux derives d'imidazole, leur procede de preparation et les compositions pharmaceutiques qui les contiennent | |
US2486445A (en) | Safrole-sulfoxide and sulfone insecticide and pyrethrin synergist | |
EP0007828B1 (fr) | Procédé de préparation d'esters d'alcoyle de l'acide dl-cis chrysanthémique | |
CA2161284C (fr) | Nouvelles o-arylmethyl n-(thio)acyl hydroxylamines, leurs procedes de preparation et les compisitions pharmaceutiques qui les contiennent | |
BE1006226A3 (fr) | Derives de la benzofuranylimidazole, leur procede de preparation ainsi qu'une composition therapeutique les contenant. | |
EP0082040B1 (fr) | Dérivés de diaza-3,7a cyclohepta(j,k)fluorènes, leur préparation et leur application en thérapeutique | |
US2716627A (en) | 1-aryl derivatives of 2-nitroisopropyl-phenylalkanes and insecticidal compositions containing the same | |
Mallipudi et al. | Synthesis and insecticidal activity of novel N-oxalyl-N-methylcarbamates | |
FR2480278A1 (fr) | Nouveaux derives du terpene, procede pour leur preparation et compositions insecticides contenant ces derives | |
CA1190235A (fr) | Procede de preparation d'esters d'acides cyclopropane carboxyliques d'allethrolone optiquement active | |
BE464617A (ja) | ||
US2719810A (en) | 1-aryl derivatives of 2-nitro-1-tetrahydronaphthylalkanes, and insecticidal compositions containing the same | |
BE880478A (fr) | Benzimidazole-carbamates | |
CH339921A (fr) | Procédé de préparation de carbamates de carbinols tertiaires |