BE582886A - - Google Patents
Info
- Publication number
- BE582886A BE582886A BE582886DA BE582886A BE 582886 A BE582886 A BE 582886A BE 582886D A BE582886D A BE 582886DA BE 582886 A BE582886 A BE 582886A
- Authority
- BE
- Belgium
- Prior art keywords
- alpha
- sep
- chlorophenyl
- seeds
- dichlorophenyl
- Prior art date
Links
- -1 alkyl radical Chemical class 0.000 claims description 25
- 150000001875 compounds Chemical class 0.000 claims description 19
- 230000000855 fungicidal effect Effects 0.000 claims description 12
- 239000004094 surface-active agent Substances 0.000 claims description 10
- 239000001257 hydrogen Substances 0.000 claims description 7
- 229910052739 hydrogen Inorganic materials 0.000 claims description 7
- 239000000203 mixture Substances 0.000 claims description 6
- 125000004201 2,4-dichlorophenyl group Chemical group [H]C1=C([H])C(*)=C(Cl)C([H])=C1Cl 0.000 claims description 5
- 238000000034 method Methods 0.000 claims description 5
- 239000007787 solid Substances 0.000 claims description 5
- 239000000080 wetting agent Substances 0.000 claims description 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 4
- 229910052801 chlorine Inorganic materials 0.000 claims description 4
- 239000000460 chlorine Substances 0.000 claims description 4
- KFARNDPRHQBGEL-UHFFFAOYSA-N 3-(2,4-dichlorophenyl)pyrrole-2,5-dione Chemical compound ClC1=CC(Cl)=CC=C1C1=CC(=O)NC1=O KFARNDPRHQBGEL-UHFFFAOYSA-N 0.000 claims description 3
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 3
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 claims description 3
- 230000001681 protective effect Effects 0.000 claims description 3
- YIYWMWTZIFFMCO-UHFFFAOYSA-N 3-(2-chlorophenyl)pyrrole-2,5-dione Chemical compound ClC1=CC=CC=C1C1=CC(=O)NC1=O YIYWMWTZIFFMCO-UHFFFAOYSA-N 0.000 claims description 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 2
- 241000233866 Fungi Species 0.000 claims description 2
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 150000005840 aryl radicals Chemical class 0.000 claims description 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 2
- 229910052794 bromium Inorganic materials 0.000 claims description 2
- WCYWZMWISLQXQU-UHFFFAOYSA-N methyl Chemical group [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 claims description 2
- WZJZMVSJWUHDOB-UHFFFAOYSA-N 3-chloropyrrolidine-2,5-dione Chemical compound ClC1CC(=O)NC1=O WZJZMVSJWUHDOB-UHFFFAOYSA-N 0.000 claims 1
- 239000004480 active ingredient Substances 0.000 claims 1
- 241000196324 Embryophyta Species 0.000 description 14
- 239000000126 substance Substances 0.000 description 13
- 239000000417 fungicide Substances 0.000 description 12
- 230000035784 germination Effects 0.000 description 10
- 239000000463 material Substances 0.000 description 9
- 239000000047 product Substances 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 125000004182 2-chlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(*)C([H])=C1[H] 0.000 description 5
- 230000001012 protector Effects 0.000 description 5
- PEEHTFAAVSWFBL-UHFFFAOYSA-N Maleimide Chemical compound O=C1NC(=O)C=C1 PEEHTFAAVSWFBL-UHFFFAOYSA-N 0.000 description 4
- 239000007921 spray Substances 0.000 description 4
- SVPKNMBRVBMTLB-UHFFFAOYSA-N 2,3-dichloronaphthalene-1,4-dione Chemical compound C1=CC=C2C(=O)C(Cl)=C(Cl)C(=O)C2=C1 SVPKNMBRVBMTLB-UHFFFAOYSA-N 0.000 description 3
- 150000003923 2,5-pyrrolediones Chemical class 0.000 description 3
- IJMBFOPCPHVSRS-UHFFFAOYSA-N 3-(4-chlorophenyl)pyrrole-2,5-dione Chemical compound C1=CC(Cl)=CC=C1C1=CC(=O)NC1=O IJMBFOPCPHVSRS-UHFFFAOYSA-N 0.000 description 3
- ZLPORNPZJNRGCO-UHFFFAOYSA-N 3-methylpyrrole-2,5-dione Chemical compound CC1=CC(=O)NC1=O ZLPORNPZJNRGCO-UHFFFAOYSA-N 0.000 description 3
- 125000005059 halophenyl group Chemical group 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 239000002689 soil Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 239000000725 suspension Substances 0.000 description 3
- 125000006276 2-bromophenyl group Chemical group [H]C1=C([H])C(Br)=C(*)C([H])=C1[H] 0.000 description 2
- BTMJLNZQSOGJMI-UHFFFAOYSA-N 3,4-dichloro-3-phenylpyrrolidine-2,5-dione Chemical class ClC1C(=O)NC(=O)C1(Cl)C1=CC=CC=C1 BTMJLNZQSOGJMI-UHFFFAOYSA-N 0.000 description 2
- MDXKEHHAIMNCSW-UHFFFAOYSA-N 3-propylpyrrole-2,5-dione Chemical compound CCCC1=CC(=O)NC1=O MDXKEHHAIMNCSW-UHFFFAOYSA-N 0.000 description 2
- JRNVZBWKYDBUCA-UHFFFAOYSA-N N-Chlorosuccinimide Substances ClN1C(=O)CCC1=O JRNVZBWKYDBUCA-UHFFFAOYSA-N 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
- 230000003902 lesion Effects 0.000 description 2
- UZIRFBMYVLTOHJ-UHFFFAOYSA-N 3-(2,4,6-trichlorophenyl)pyrrole-2,5-dione Chemical compound ClC1=CC(Cl)=CC(Cl)=C1C1=CC(=O)NC1=O UZIRFBMYVLTOHJ-UHFFFAOYSA-N 0.000 description 1
- MPBBSRNQYJLMDP-UHFFFAOYSA-N 3-(2,4-dichlorophenyl)-1-methylpyrrole-2,5-dione Chemical compound O=C1N(C)C(=O)C=C1C1=CC=C(Cl)C=C1Cl MPBBSRNQYJLMDP-UHFFFAOYSA-N 0.000 description 1
- MWMAJOGHZCKELR-UHFFFAOYSA-N 3-(4-chlorophenyl)-1-(4-methylphenyl)pyrrole-2,5-dione Chemical compound C1=CC(C)=CC=C1N1C(=O)C(C=2C=CC(Cl)=CC=2)=CC1=O MWMAJOGHZCKELR-UHFFFAOYSA-N 0.000 description 1
- LGXGCMJVZWBFSV-UHFFFAOYSA-N 3-(4-methoxyphenyl)pyrrole-2,5-dione Chemical compound C1=CC(OC)=CC=C1C1=CC(=O)NC1=O LGXGCMJVZWBFSV-UHFFFAOYSA-N 0.000 description 1
- 125000004179 3-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(Cl)=C1[H] 0.000 description 1
- 241000213004 Alternaria solani Species 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- 206010061217 Infestation Diseases 0.000 description 1
- 229930192627 Naphthoquinone Natural products 0.000 description 1
- 240000003768 Solanum lycopersicum Species 0.000 description 1
- 239000000443 aerosol Substances 0.000 description 1
- 238000001856 aerosol method Methods 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000007900 aqueous suspension Substances 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 235000013339 cereals Nutrition 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- 125000000068 chlorophenyl group Chemical group 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 235000013399 edible fruits Nutrition 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 150000002431 hydrogen Chemical group 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 229910052909 inorganic silicate Inorganic materials 0.000 description 1
- 239000008263 liquid aerosol Substances 0.000 description 1
- 238000005461 lubrication Methods 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 150000002791 naphthoquinones Chemical class 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000003223 protective agent Substances 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 239000004563 wettable powder Substances 0.000 description 1
Landscapes
- Agricultural Chemicals And Associated Chemicals (AREA)
Publications (1)
| Publication Number | Publication Date |
|---|---|
| BE582886A true BE582886A (enrdf_load_stackoverflow) |
Family
ID=191340
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BE582886D BE582886A (enrdf_load_stackoverflow) |
Country Status (1)
| Country | Link |
|---|---|
| BE (1) | BE582886A (enrdf_load_stackoverflow) |
-
0
- BE BE582886D patent/BE582886A/fr unknown
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| FR2684519A1 (fr) | Association d'un fongicide de la famille des triazoles et d'imidacloprid. | |
| EP0781508B1 (fr) | Mélanges herbicides à base de flurtamone et d'un composé 3-phénylpyrazole | |
| CA1300496C (fr) | Compositions contenant des produits pesticides biosynthetiques, procedes pour leur production et leur utilisation | |
| BE529063A (enrdf_load_stackoverflow) | ||
| LU87064A1 (fr) | Procede pour combattre les maladies fongiques des plantes a l'aide d'une composition a base de carbendazime | |
| CH427400A (fr) | Composition fongicide | |
| BE582886A (enrdf_load_stackoverflow) | ||
| BE574921A (enrdf_load_stackoverflow) | ||
| FR2582647A1 (fr) | Derives du phenanthrene, leur procede de preparation et compositions fongicides les contenant | |
| JPH07188183A (ja) | （４−シクロプロピル−６−メチル−ピリミジニ−２−イル）−フェニル−アミンの結晶変態方法 | |
| EP0663148B1 (fr) | Composition fongicide à base d'un 3,5-dichloranilide comme l'iprodione et de bromocunazole | |
| LU85259A1 (fr) | Ester de l'hydroxyde de tricyclohexyletain acaricide | |
| FR2737085A1 (fr) | Associations insecticides d'un oxime carbamate avec un insecticide a groupe pyrazole ou phenylimidazole | |
| EP0021939B1 (fr) | Hydrazino (ou azido) alkylthio-5 pyrimidines, leurs procédés de préparation et leurs utilisations comme herbicides et fongicides | |
| FR2640116A1 (fr) | Composition biocide stable pour l'application industrielle | |
| BE818849A (fr) | Derives de cyclohexane | |
| LU86116A1 (fr) | Compositions herbicides selectives ayant une action prolongee et contenant,a titre d'ingredient actif,des derives d'alpha-chloracetamide | |
| US4139622A (en) | Method of controlling fungi using phthalazine compounds | |
| CH618679A5 (enrdf_load_stackoverflow) | ||
| US4225599A (en) | Use of 1-lower alkoxy-4-trichloromethylphthalazines as an insecticide | |
| BE550303A (enrdf_load_stackoverflow) | ||
| CA1256884A (en) | Process for producing 3-cyano-4-phenylpyrroles | |
| FR2471371A1 (fr) | Derive d'uree, procede d'obtention compositions herbicides le contenant et procede pour lutter contre les mauvaises herbes au moyen de celui-ci | |
| JPH0649007A (ja) | 殺菌性組成物 | |
| BE581720A (enrdf_load_stackoverflow) |