IL32202A - 1-alkoxy-or-aryloxy-1-thiono-3-halogen-or-3-alkyl phospholines,their preparation and use for combatting pests - Google Patents
1-alkoxy-or-aryloxy-1-thiono-3-halogen-or-3-alkyl phospholines,their preparation and use for combatting pestsInfo
- Publication number
- IL32202A IL32202A IL32202A IL3220269A IL32202A IL 32202 A IL32202 A IL 32202A IL 32202 A IL32202 A IL 32202A IL 3220269 A IL3220269 A IL 3220269A IL 32202 A IL32202 A IL 32202A
- Authority
- IL
- Israel
- Prior art keywords
- process according
- solvent
- pests
- thiono
- preparation
- Prior art date
Links
- 241000607479 Yersinia pestis Species 0.000 title claims description 9
- 238000002360 preparation method Methods 0.000 title description 9
- 150000001875 compounds Chemical class 0.000 claims description 19
- 238000000034 method Methods 0.000 claims description 11
- 239000003085 diluting agent Substances 0.000 claims description 8
- 239000002904 solvent Substances 0.000 claims description 8
- 239000007788 liquid Substances 0.000 claims description 7
- 239000000203 mixture Substances 0.000 claims description 7
- 238000006243 chemical reaction Methods 0.000 claims description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 5
- 241000244206 Nematoda Species 0.000 claims description 5
- 239000007787 solid Substances 0.000 claims description 5
- 239000002689 soil Substances 0.000 claims description 4
- 241000233866 Fungi Species 0.000 claims description 3
- 230000000895 acaricidal effect Effects 0.000 claims description 3
- 241000238631 Hexapoda Species 0.000 claims description 2
- 239000002253 acid Substances 0.000 claims description 2
- 239000004480 active ingredient Substances 0.000 claims description 2
- 229960002017 echothiophate Drugs 0.000 claims description 2
- 230000000749 insecticidal effect Effects 0.000 claims description 2
- 239000003960 organic solvent Substances 0.000 claims description 2
- 239000000376 reactant Substances 0.000 claims description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims 2
- 239000011230 binding agent Substances 0.000 claims 1
- 230000000855 fungicidal effect Effects 0.000 claims 1
- 229910052736 halogen Inorganic materials 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 230000001069 nematicidal effect Effects 0.000 claims 1
- 239000004094 surface-active agent Substances 0.000 claims 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 125000003118 aryl group Chemical group 0.000 description 3
- 239000012141 concentrate Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000003995 emulsifying agent Substances 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- 230000003032 phytopathogenic effect Effects 0.000 description 3
- 241000255925 Diptera Species 0.000 description 2
- 241000399949 Ditylenchus dipsaci Species 0.000 description 2
- 241001465754 Metazoa Species 0.000 description 2
- -1 aliphatic aromatic hydrocarbons Chemical class 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 230000001988 toxicity Effects 0.000 description 2
- 231100000419 toxicity Toxicity 0.000 description 2
- ZYVYEJXMYBUCMN-UHFFFAOYSA-N 1-methoxy-2-methylpropane Chemical class COCC(C)C ZYVYEJXMYBUCMN-UHFFFAOYSA-N 0.000 description 1
- ONNDGYXYNGPSJT-UHFFFAOYSA-N 2,2-diethyl-1,4-dioxane Chemical compound CCC1(CC)COCCO1 ONNDGYXYNGPSJT-UHFFFAOYSA-N 0.000 description 1
- 241000238818 Acheta domesticus Species 0.000 description 1
- 241000256111 Aedes <genus> Species 0.000 description 1
- 241000256186 Anopheles <genus> Species 0.000 description 1
- 241000680417 Aphelenchoides ritzemabosi Species 0.000 description 1
- 241001425390 Aphis fabae Species 0.000 description 1
- 241000239290 Araneae Species 0.000 description 1
- 241000387313 Aspidiotus Species 0.000 description 1
- 241000238657 Blattella germanica Species 0.000 description 1
- 241000238678 Boophilus Species 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
- 241000255579 Ceratitis capitata Species 0.000 description 1
- 241000191839 Chrysomya Species 0.000 description 1
- 241000254171 Curculionidae Species 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 241001442497 Globodera rostochiensis Species 0.000 description 1
- 241001659689 Hercinothrips Species 0.000 description 1
- 241000379510 Heterodera schachtii Species 0.000 description 1
- 241000736227 Lucilia sericata Species 0.000 description 1
- 241000243786 Meloidogyne incognita Species 0.000 description 1
- 241000257159 Musca domestica Species 0.000 description 1
- 241001481099 Ornithodoros turicata Species 0.000 description 1
- 240000007594 Oryza sativa Species 0.000 description 1
- 235000007164 Oryza sativa Nutrition 0.000 description 1
- 241000488583 Panonychus ulmi Species 0.000 description 1
- 241001548358 Parapiesma quadratum Species 0.000 description 1
- 241001148650 Paratylenchus Species 0.000 description 1
- 244000046052 Phaseolus vulgaris Species 0.000 description 1
- 241000500439 Plutella Species 0.000 description 1
- 241000500437 Plutella xylostella Species 0.000 description 1
- 241000722234 Pseudococcus Species 0.000 description 1
- 241001509970 Reticulitermes <genus> Species 0.000 description 1
- 235000001537 Ribes X gardonianum Nutrition 0.000 description 1
- 235000001535 Ribes X utile Nutrition 0.000 description 1
- 235000016919 Ribes petraeum Nutrition 0.000 description 1
- 244000281247 Ribes rubrum Species 0.000 description 1
- 235000002355 Ribes spicatum Nutrition 0.000 description 1
- 240000000111 Saccharum officinarum Species 0.000 description 1
- 244000061456 Solanum tuberosum Species 0.000 description 1
- 235000002595 Solanum tuberosum Nutrition 0.000 description 1
- 241001454295 Tetranychidae Species 0.000 description 1
- 241000201423 Xiphinema Species 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 125000002877 alkyl aryl group Chemical group 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 230000004071 biological effect Effects 0.000 description 1
- 239000012043 crude product Substances 0.000 description 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- XXBDWLFCJWSEKW-UHFFFAOYSA-N dimethylbenzylamine Chemical compound CN(C)CC1=CC=CC=C1 XXBDWLFCJWSEKW-UHFFFAOYSA-N 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000010410 dusting Methods 0.000 description 1
- BJOLKYGKSZKIGU-UHFFFAOYSA-N ecothiopate Chemical compound CCOP(=O)(OCC)SCC[N+](C)(C)C BJOLKYGKSZKIGU-UHFFFAOYSA-N 0.000 description 1
- 239000004495 emulsifiable concentrate Substances 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000012074 organic phase Substances 0.000 description 1
- 230000000361 pesticidal effect Effects 0.000 description 1
- 229920000151 polyglycol Polymers 0.000 description 1
- 239000010695 polyglycol Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 238000000926 separation method Methods 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
- 239000007921 spray Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 238000003809 water extraction Methods 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 150000003738 xylenes Chemical class 0.000 description 1
Classifications
-
- 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
- C07F9/6564—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms
- C07F9/6568—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms having phosphorus atoms as the only ring hetero atoms
- C07F9/65681—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms having phosphorus atoms as the only ring hetero atoms the ring phosphorus atom being part of a (thio)phosphinic acid or ester thereof
-
- 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
-
- 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
- A01N57/36—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus as a ring member
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- Plant Pathology (AREA)
- Pest Control & Pesticides (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Organic Chemistry (AREA)
- Biochemistry (AREA)
- Molecular Biology (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19681768662 DE1768662C3 (de) | 1968-06-14 | 1 -Alkoxy- bzw.1 -Aryloxy-1 -thiono-3halogen- bzw. -3-alkylphospholine, Verfahren zu ihrer Herstellung und ihre Verwendung |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| IL32202A0 IL32202A0 (en) | 1969-07-30 |
| IL32202A true IL32202A (en) | 1972-08-30 |
Family
ID=5699822
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IL32202A IL32202A (en) | 1968-06-14 | 1969-05-11 | 1-alkoxy-or-aryloxy-1-thiono-3-halogen-or-3-alkyl phospholines,their preparation and use for combatting pests |
Country Status (11)
| Country | Link |
|---|---|
| US (2) | US3644598A (xx) |
| JP (1) | JPS4913967B1 (xx) |
| AT (1) | AT292379B (xx) |
| BE (1) | BE734411A (xx) |
| CH (1) | CH511254A (xx) |
| DK (1) | DK124759B (xx) |
| ES (1) | ES368292A1 (xx) |
| FR (1) | FR2010911A1 (xx) |
| GB (1) | GB1237658A (xx) |
| IL (1) | IL32202A (xx) |
| NL (1) | NL6909053A (xx) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5199869U (xx) * | 1975-02-07 | 1976-08-11 | ||
| JPS5285768A (en) * | 1976-01-09 | 1977-07-16 | Kanebo Ltd | Top feed type continuous dewatering machine in which material to be fi ltered is run |
| JPS5333270U (xx) * | 1976-08-28 | 1978-03-23 | ||
| JPS5467868U (xx) * | 1978-07-28 | 1979-05-14 |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2761806A (en) * | 1954-10-27 | 1956-09-04 | Virginia Carolina Chem Corp | Method of controlling nematodes in the soil |
| US3285999A (en) * | 1963-06-07 | 1966-11-15 | Continental Oil Co | Thioamidophospholanes |
-
1969
- 1969-05-11 IL IL32202A patent/IL32202A/en unknown
- 1969-05-14 CH CH740269A patent/CH511254A/de not_active IP Right Cessation
- 1969-06-03 US US830122A patent/US3644598A/en not_active Expired - Lifetime
- 1969-06-04 AT AT530869A patent/AT292379B/de active
- 1969-06-09 GB GB28973/69A patent/GB1237658A/en not_active Expired
- 1969-06-11 JP JP44045709A patent/JPS4913967B1/ja active Pending
- 1969-06-11 BE BE734411D patent/BE734411A/xx unknown
- 1969-06-12 ES ES368292A patent/ES368292A1/es not_active Expired
- 1969-06-13 FR FR6919733A patent/FR2010911A1/fr not_active Withdrawn
- 1969-06-13 DK DK320069AA patent/DK124759B/da unknown
- 1969-06-13 NL NL6909053A patent/NL6909053A/xx unknown
-
1971
- 1971-08-20 US US00173677A patent/US3726973A/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| BE734411A (xx) | 1969-12-11 |
| JPS4913967B1 (xx) | 1974-04-04 |
| AT292379B (de) | 1971-08-25 |
| ES368292A1 (es) | 1971-05-01 |
| DE1768662A1 (de) | 1971-10-28 |
| NL6909053A (xx) | 1969-12-16 |
| US3726973A (en) | 1973-04-10 |
| CH511254A (de) | 1971-08-15 |
| DK124759B (da) | 1972-11-20 |
| US3644598A (en) | 1972-02-22 |
| FR2010911A1 (xx) | 1970-02-20 |
| IL32202A0 (en) | 1969-07-30 |
| DE1768662B2 (de) | 1975-10-09 |
| GB1237658A (en) | 1971-06-30 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE69217085T2 (de) | Insekttötende phenylhydrazin-derivate | |
| US4210642A (en) | Insecticidal and acaricidal compositions | |
| IL32202A (en) | 1-alkoxy-or-aryloxy-1-thiono-3-halogen-or-3-alkyl phospholines,their preparation and use for combatting pests | |
| US3678075A (en) | Carbamoyloximino-alkenyl-dithiolanes | |
| IL33176A (en) | Phosphoric,phosphonic,thionophosphonic and thionophosphoric acid esters,their preparation and use for combatting pests | |
| DE2303185C2 (de) | Thiophosphorsäurephenylester, Verfahren zu ihrer Herstellung sowie diese enthaltende Schädlingsbekämpfungsmittel | |
| US3492335A (en) | Alkoxy-alkoxyphenyl-n-methyl-carbamates | |
| US3476490A (en) | Methods of using particular carbamic acid esters for insecticidal and acaricidal purposes | |
| US3437684A (en) | 3,5-dimethyl-4-alpha-allyl mercaptophenyl-n-methyl carbamic acid ester | |
| US3590074A (en) | Chlor-methyl-isopropyl-phenyl-n-methyl carbamate | |
| US3781331A (en) | N-trihalomethanesulfenyl-n-methyl-carbamates | |
| US3083137A (en) | 3, 5-diisopropylphenyl n-methylcarbamate, a low toxicity insecticide | |
| CH616687A5 (xx) | ||
| IL27735A (en) | Carbamate oxen, their preparation and use in insecticides and acaricides | |
| US3455912A (en) | Benzodioxan-n-methylcarbamates | |
| US3470229A (en) | O,o-dialkyl-o-(dithiocarbonato) ethyl-phosphoric acid esters | |
| US3453316A (en) | 4-(n-methyl-n-allyl-amino)-phenyl-n'-methyl carbamates | |
| US3886273A (en) | Certain thiophosphate synergists | |
| US3641222A (en) | S.s-dialkyl-amido-dithiophosphates | |
| US4686209A (en) | Certain N-(substituted-aminosulfinyl)phosphonamidothioate and dithioate pesticides | |
| US4071556A (en) | Formamidine insecticidal compounds | |
| US4216213A (en) | Acaricidal and insecticidal compositions | |
| US3284547A (en) | Phosphoric esters | |
| US3773942A (en) | Carbamoyloximino alkenyl-dithiolones used as insecticides | |
| US4390549A (en) | N-Tetrachloroethylthio benzoyl anilides useful as acaricides and to control mosquitoes |