FR2484198A1 - Derives du thiazole a titre de produits fongicides, application a la lutte contre les champignons parasites et compositions les renfermant - Google Patents
Derives du thiazole a titre de produits fongicides, application a la lutte contre les champignons parasites et compositions les renfermant Download PDFInfo
- Publication number
- FR2484198A1 FR2484198A1 FR8012961A FR8012961A FR2484198A1 FR 2484198 A1 FR2484198 A1 FR 2484198A1 FR 8012961 A FR8012961 A FR 8012961A FR 8012961 A FR8012961 A FR 8012961A FR 2484198 A1 FR2484198 A1 FR 2484198A1
- Authority
- FR
- France
- Prior art keywords
- sep
- formula
- derivatives
- product
- carbon atoms
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000000417 fungicide Substances 0.000 title abstract description 4
- FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical compound C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 title abstract 2
- IOJUPLGTWVMSFF-UHFFFAOYSA-N benzothiazole Chemical compound C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 title 2
- ZZUFCTLCJUWOSV-UHFFFAOYSA-N furosemide Chemical compound C1=C(Cl)C(S(=O)(=O)N)=CC(C(O)=O)=C1NCC1=CC=CO1 ZZUFCTLCJUWOSV-UHFFFAOYSA-N 0.000 title 1
- 125000002947 alkylene group Chemical group 0.000 claims abstract description 3
- -1 alkyl radical Chemical class 0.000 claims description 11
- 230000000855 fungicidal effect Effects 0.000 claims description 9
- 125000004432 carbon atom Chemical group C* 0.000 claims description 8
- 239000000203 mixture Substances 0.000 claims description 8
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 7
- QUPDWYMUPZLYJZ-UHFFFAOYSA-N ethyl Chemical compound C[CH2] QUPDWYMUPZLYJZ-UHFFFAOYSA-N 0.000 claims description 6
- 241000233866 Fungi Species 0.000 claims description 5
- 150000001875 compounds Chemical class 0.000 claims description 4
- 150000003254 radicals Chemical class 0.000 claims description 4
- 150000007979 thiazole derivatives Chemical class 0.000 claims description 4
- 239000004480 active ingredient Substances 0.000 claims description 3
- 230000003071 parasitic effect Effects 0.000 claims description 3
- 238000000034 method Methods 0.000 claims description 2
- RMFVVPBBEDMZQI-UHFFFAOYSA-N 4,5,6,7-tetrahydro-1,3-benzothiazole Chemical compound C1CCCC2=C1N=CS2 RMFVVPBBEDMZQI-UHFFFAOYSA-N 0.000 claims 1
- 239000000843 powder Substances 0.000 abstract description 4
- 239000000725 suspension Substances 0.000 abstract description 4
- 230000000895 acaricidal effect Effects 0.000 abstract description 3
- 239000000642 acaricide Substances 0.000 abstract description 2
- 239000000839 emulsion Substances 0.000 abstract description 2
- 239000008187 granular material Substances 0.000 abstract description 2
- 239000003630 growth substance Substances 0.000 abstract description 2
- 239000002917 insecticide Substances 0.000 abstract description 2
- 125000000217 alkyl group Chemical group 0.000 abstract 3
- HYZJCKYKOHLVJF-UHFFFAOYSA-N 1H-benzimidazole Chemical compound C1=CC=C2NC=NC2=C1 HYZJCKYKOHLVJF-UHFFFAOYSA-N 0.000 abstract 1
- 239000000969 carrier Substances 0.000 abstract 1
- 231100001184 nonphytotoxic Toxicity 0.000 abstract 1
- 239000004094 surface-active agent Substances 0.000 abstract 1
- 241000196324 Embryophyta Species 0.000 description 8
- 239000002002 slurry Substances 0.000 description 5
- 241001480061 Blumeria graminis Species 0.000 description 4
- 206010061217 Infestation Diseases 0.000 description 4
- 201000010099 disease Diseases 0.000 description 4
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 4
- 238000011534 incubation Methods 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 235000021395 porridge Nutrition 0.000 description 4
- 240000008067 Cucumis sativus Species 0.000 description 3
- 241000209219 Hordeum Species 0.000 description 3
- 235000007340 Hordeum vulgare Nutrition 0.000 description 3
- 241001281803 Plasmopara viticola Species 0.000 description 3
- 241000209140 Triticum Species 0.000 description 3
- 235000021307 Triticum Nutrition 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 2
- 241000896246 Golovinomyces cichoracearum Species 0.000 description 2
- FPIPGXGPPPQFEQ-OVSJKPMPSA-N all-trans-retinol Chemical compound OC\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-OVSJKPMPSA-N 0.000 description 2
- RIOXQFHNBCKOKP-UHFFFAOYSA-N benomyl Chemical compound C1=CC=C2N(C(=O)NCCCC)C(NC(=O)OC)=NC2=C1 RIOXQFHNBCKOKP-UHFFFAOYSA-N 0.000 description 2
- TWFZGCMQGLPBSX-UHFFFAOYSA-N carbendazim Chemical compound C1=CC=C2NC(NC(=O)OC)=NC2=C1 TWFZGCMQGLPBSX-UHFFFAOYSA-N 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- YKSNLCVSTHTHJA-UHFFFAOYSA-L maneb Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S YKSNLCVSTHTHJA-UHFFFAOYSA-L 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 159000000000 sodium salts Chemical class 0.000 description 2
- 241000894007 species Species 0.000 description 2
- 239000000454 talc Substances 0.000 description 2
- 229910052623 talc Inorganic materials 0.000 description 2
- 239000004563 wettable powder Substances 0.000 description 2
- VPGSXIKVUASQIY-UHFFFAOYSA-N 1,2-dibutylnaphthalene Chemical compound C1=CC=CC2=C(CCCC)C(CCCC)=CC=C21 VPGSXIKVUASQIY-UHFFFAOYSA-N 0.000 description 1
- WPWHSFAFEBZWBB-UHFFFAOYSA-N 1-butyl radical Chemical compound [CH2]CCC WPWHSFAFEBZWBB-UHFFFAOYSA-N 0.000 description 1
- YTOPFCCWCSOHFV-UHFFFAOYSA-N 2,6-dimethyl-4-tridecylmorpholine Chemical compound CCCCCCCCCCCCCN1CC(C)OC(C)C1 YTOPFCCWCSOHFV-UHFFFAOYSA-N 0.000 description 1
- PNXAXJVLYZOWEB-UHFFFAOYSA-N 2-(2,2,2-trichloroethylsulfanyl)isoindole-1,3-dione Chemical compound ClC(CSN1C(C=2C(C1=O)=CC=CC2)=O)(Cl)Cl PNXAXJVLYZOWEB-UHFFFAOYSA-N 0.000 description 1
- HNUALPPJLMYHDK-UHFFFAOYSA-N C[CH]C Chemical compound C[CH]C HNUALPPJLMYHDK-UHFFFAOYSA-N 0.000 description 1
- 241001157813 Cercospora Species 0.000 description 1
- 235000009849 Cucumis sativus Nutrition 0.000 description 1
- 235000010799 Cucumis sativus var sativus Nutrition 0.000 description 1
- 206010061818 Disease progression Diseases 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- 208000031888 Mycoses Diseases 0.000 description 1
- 241000233679 Peronosporaceae Species 0.000 description 1
- 241000221300 Puccinia Species 0.000 description 1
- 241000813090 Rhizoctonia solani Species 0.000 description 1
- 239000011149 active material Substances 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 239000011717 all-trans-retinol Substances 0.000 description 1
- 235000019169 all-trans-retinol Nutrition 0.000 description 1
- 239000010775 animal oil Substances 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 229940058303 antinematodal benzimidazole derivative Drugs 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 150000001556 benzimidazoles Chemical class 0.000 description 1
- MITFXPHMIHQXPI-UHFFFAOYSA-N benzoxaprofen Natural products N=1C2=CC(C(C(O)=O)C)=CC=C2OC=1C1=CC=C(Cl)C=C1 MITFXPHMIHQXPI-UHFFFAOYSA-N 0.000 description 1
- 239000006013 carbendazim Substances 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 239000003093 cationic surfactant Substances 0.000 description 1
- 235000013339 cereals Nutrition 0.000 description 1
- 230000005750 disease progression Effects 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000010410 dusting Methods 0.000 description 1
- 235000013399 edible fruits Nutrition 0.000 description 1
- CZWCQRFMTZHZLB-UHFFFAOYSA-N ethyl 4,5,6,7-tetrahydro-1,3-benzothiazole-4-carboxylate Chemical compound CCOC(=O)C1CCCC2=C1N=CS2 CZWCQRFMTZHZLB-UHFFFAOYSA-N 0.000 description 1
- 239000003337 fertilizer Substances 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 230000000749 insecticidal effect Effects 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 229920005610 lignin Polymers 0.000 description 1
- 229920000940 maneb Polymers 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 230000003449 preventive effect Effects 0.000 description 1
- 230000000069 prophylactic effect Effects 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 235000013311 vegetables 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
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/10—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds
- A01N57/16—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds containing heterocyclic radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6536—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having nitrogen and sulfur atoms with or without oxygen atoms, as the only ring hetero atoms
- C07F9/6539—Five-membered rings
- C07F9/6541—Five-membered rings condensed with carbocyclic rings or carbocyclic ring systems
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Dentistry (AREA)
- Engineering & Computer Science (AREA)
- Plant Pathology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Biochemistry (AREA)
- Molecular Biology (AREA)
- Agronomy & Crop Science (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR8012961A FR2484198A1 (fr) | 1980-06-11 | 1980-06-11 | Derives du thiazole a titre de produits fongicides, application a la lutte contre les champignons parasites et compositions les renfermant |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR8012961A FR2484198A1 (fr) | 1980-06-11 | 1980-06-11 | Derives du thiazole a titre de produits fongicides, application a la lutte contre les champignons parasites et compositions les renfermant |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| FR2484198A1 true FR2484198A1 (fr) | 1981-12-18 |
| FR2484198B1 FR2484198B1 (OSRAM) | 1984-05-04 |
Family
ID=9242960
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| FR8012961A Granted FR2484198A1 (fr) | 1980-06-11 | 1980-06-11 | Derives du thiazole a titre de produits fongicides, application a la lutte contre les champignons parasites et compositions les renfermant |
Country Status (1)
| Country | Link |
|---|---|
| FR (1) | FR2484198A1 (OSRAM) |
-
1980
- 1980-06-11 FR FR8012961A patent/FR2484198A1/fr active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| FR2484198B1 (OSRAM) | 1984-05-04 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| BE898070A (fr) | Nouveaux derives de l'ethanol, leur preparation et leur utilisation comme fongicides. | |
| FR2542000A1 (fr) | Nouveaux derives de l'ethanol, leur preparation et leur utilisation comme fongicides | |
| FR2551438A1 (fr) | Nouveaux derives de l'ethanol, leur preparation et leur utilisation comme fongicides | |
| FR2607669A1 (fr) | Procede pour combattre les maladies fongiques des plantes a l'aide d'une composition a base de carbendazime | |
| JPS6021965B2 (ja) | 殺菌剤 | |
| EP0599749A1 (fr) | Dérivés de 2-alkoxy 2-imidazoline-5 ones fongicides | |
| EP0230844B1 (fr) | Fongicides à groupes triazole et oligoéther et associations | |
| FI68498C (fi) | Blandning foer bekaempning av fytopatogeniska svampar och bakterier | |
| FR2484198A1 (fr) | Derives du thiazole a titre de produits fongicides, application a la lutte contre les champignons parasites et compositions les renfermant | |
| FR2486079A1 (fr) | Sels quaternaires d'alcoyl-1-imidazolium de l'acide phosphoreux ou ses monoesters, procedes pour les preparer et compositions fongicides les contenant | |
| EP0068296B1 (en) | a new fungicidal composition, processes for its production and its use | |
| US3652770A (en) | Combatting phytopathogenic fungi on plants with sub-phytotoxic fungicidally effective amounts of herbicidal oximes of 3 5-dihalosalicylaldehyde | |
| FR2582647A1 (fr) | Derives du phenanthrene, leur procede de preparation et compositions fongicides les contenant | |
| PL120771B1 (en) | Fungicide | |
| FR2465417A1 (fr) | Produit et composition acaricides et procede de destruction des tiques et des acariens | |
| FR2588724A1 (fr) | Compositions fongicides a base de derive du triazole et leur utilisation | |
| CH657505A5 (fr) | Composition fongicide a base d'un melange de matiere active. | |
| EP0318400A1 (fr) | Composés à groupements triazole, utilisation de ceux-ci à titre de fongicides et procédés de préparation | |
| FR2598708A1 (fr) | Compositions fongicides a base de derives nicotiniques, nouveaux derives nicotiniques et leur preparation | |
| FR2598408A1 (fr) | Derives propargyloxybenzenes : leur preparation et compositions fongicides les contenant | |
| DE2226301A1 (de) | Alkyl-1-(n-substituierte thiocarbamoyl)-2-benzimidazolcarbamate | |
| BE889317Q (fr) | Arylhydrazo-aldoximes nouveaux et leur emploi en tant que fongicides | |
| FR2548665A1 (fr) | Nouveaux derives de l'ethanol, leur preparation et leur utilisation comme fongicides | |
| US3577451A (en) | Sulfamide derivatives | |
| FR2530925A1 (fr) | Formulations fongicides a base de soufre et de pyrimidine |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| ST | Notification of lapse |