IL44555A - Pyrimidyl (thio)phosphoric acid esters - Google Patents
Pyrimidyl (thio)phosphoric acid estersInfo
- Publication number
- IL44555A IL44555A IL44555A IL4455574A IL44555A IL 44555 A IL44555 A IL 44555A IL 44555 A IL44555 A IL 44555A IL 4455574 A IL4455574 A IL 4455574A IL 44555 A IL44555 A IL 44555A
- Authority
- IL
- Israel
- Prior art keywords
- compositions
- insecticidal
- active ingredient
- diluent
- compounds
- Prior art date
Links
- -1 Pyrimidyl (thio)phosphoric acid esters Chemical class 0.000 title claims description 3
- 150000001875 compounds Chemical class 0.000 claims description 38
- 239000000203 mixture Substances 0.000 claims description 30
- 241000607479 Yersinia pestis Species 0.000 claims description 22
- 239000004480 active ingredient Substances 0.000 claims description 21
- 238000002360 preparation method Methods 0.000 claims description 14
- 238000000034 method Methods 0.000 claims description 12
- 239000003085 diluting agent Substances 0.000 claims description 11
- 230000000749 insecticidal effect Effects 0.000 claims description 11
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical group CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 claims description 9
- 239000002904 solvent Substances 0.000 claims description 9
- 239000002917 insecticide Substances 0.000 claims description 5
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 4
- 239000005864 Sulphur Chemical group 0.000 claims description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 239000000460 chlorine Substances 0.000 claims description 4
- 229910052801 chlorine Inorganic materials 0.000 claims description 4
- 239000008187 granular material Substances 0.000 claims description 4
- 229910052739 hydrogen Inorganic materials 0.000 claims description 4
- 239000001257 hydrogen Substances 0.000 claims description 4
- 239000007788 liquid Substances 0.000 claims description 4
- 229910052760 oxygen Inorganic materials 0.000 claims description 4
- 239000001301 oxygen Substances 0.000 claims description 4
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical group [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 claims description 4
- 239000000080 wetting agent Substances 0.000 claims description 4
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 3
- 206010061217 Infestation Diseases 0.000 claims description 3
- 239000002585 base Substances 0.000 claims description 3
- 239000002270 dispersing agent Substances 0.000 claims description 3
- 239000003995 emulsifying agent Substances 0.000 claims description 3
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 2
- 229910019142 PO4 Inorganic materials 0.000 claims description 2
- 229910052783 alkali metal Inorganic materials 0.000 claims description 2
- 125000003545 alkoxy group Chemical group 0.000 claims description 2
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 2
- 230000000855 fungicidal effect Effects 0.000 claims description 2
- 239000000417 fungicide Substances 0.000 claims description 2
- 229910052736 halogen Inorganic materials 0.000 claims description 2
- 125000005843 halogen group Chemical group 0.000 claims description 2
- 150000002367 halogens Chemical class 0.000 claims description 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
- 239000010452 phosphate Substances 0.000 claims description 2
- 229910000027 potassium carbonate Inorganic materials 0.000 claims description 2
- 239000007787 solid Substances 0.000 claims description 2
- 238000009736 wetting Methods 0.000 claims description 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 1
- 229910052794 bromium Chemical group 0.000 claims 1
- 125000001309 chloro group Chemical group Cl* 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 241000238631 Hexapoda Species 0.000 description 6
- SWXVUIWOUIDPGS-UHFFFAOYSA-N diacetone alcohol Chemical compound CC(=O)CC(C)(C)O SWXVUIWOUIDPGS-UHFFFAOYSA-N 0.000 description 6
- 239000012141 concentrate Substances 0.000 description 5
- 239000006185 dispersion Substances 0.000 description 4
- 238000002844 melting Methods 0.000 description 4
- 230000008018 melting Effects 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- 241000196324 Embryophyta Species 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000008262 pumice Substances 0.000 description 3
- 239000007921 spray Substances 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- 241000256118 Aedes aegypti Species 0.000 description 2
- 241001124076 Aphididae Species 0.000 description 2
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
- 241001608567 Phaedon cochleariae Species 0.000 description 2
- 241000255969 Pieris brassicae Species 0.000 description 2
- 241000500437 Plutella xylostella Species 0.000 description 2
- KMJJJTCKNZYTEY-UHFFFAOYSA-N chloro-diethoxy-sulfanylidene-$l^{5}-phosphane Chemical compound CCOP(Cl)(=S)OCC KMJJJTCKNZYTEY-UHFFFAOYSA-N 0.000 description 2
- 238000010410 dusting Methods 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- CWLLGCJZWOJVPK-UHFFFAOYSA-N 2-(dimethylamino)-6-(trifluoromethyl)-1h-pyrimidin-4-one Chemical compound CN(C)C1=NC(=O)C=C(C(F)(F)F)N1 CWLLGCJZWOJVPK-UHFFFAOYSA-N 0.000 description 1
- SCVJRXQHFJXZFZ-KVQBGUIXSA-N 2-amino-9-[(2r,4s,5r)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-3h-purine-6-thione Chemical compound C1=2NC(N)=NC(=S)C=2N=CN1[C@H]1C[C@H](O)[C@@H](CO)O1 SCVJRXQHFJXZFZ-KVQBGUIXSA-N 0.000 description 1
- HAEVLZUBSLBWIX-UHFFFAOYSA-N 2-octylphenol;oxirane Chemical compound C1CO1.CCCCCCCCC1=CC=CC=C1O HAEVLZUBSLBWIX-UHFFFAOYSA-N 0.000 description 1
- 241001425390 Aphis fabae Species 0.000 description 1
- 241000256113 Culicidae Species 0.000 description 1
- 241000257226 Muscidae Species 0.000 description 1
- 241000131102 Oryzaephilus Species 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 241000254179 Sitophilus granarius Species 0.000 description 1
- 241000344246 Tetranychus cinnabarinus Species 0.000 description 1
- 229920005551 calcium lignosulfonate Polymers 0.000 description 1
- XFBJRFNXPUCPKU-UHFFFAOYSA-N chloro-dimethoxy-sulfanylidene-$l^{5}-phosphane Chemical compound COP(Cl)(=S)OC XFBJRFNXPUCPKU-UHFFFAOYSA-N 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- LGTLXDJOAJDFLR-UHFFFAOYSA-N diethyl chlorophosphate Chemical compound CCOP(Cl)(=O)OCC LGTLXDJOAJDFLR-UHFFFAOYSA-N 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 150000002903 organophosphorus compounds Chemical class 0.000 description 1
- 230000000361 pesticidal effect Effects 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 125000000714 pyrimidinyl group Chemical group 0.000 description 1
- 238000006748 scratching Methods 0.000 description 1
- 230000002393 scratching effect Effects 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000012258 stirred mixture Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 231100000925 very toxic Toxicity 0.000 description 1
- 238000005406 washing Methods 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
- C07F9/645—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having two nitrogen atoms as the only ring hetero atoms
- C07F9/6509—Six-membered rings
- C07F9/6512—Six-membered rings having the nitrogen atoms in positions 1 and 3
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Molecular Biology (AREA)
- Agronomy & Crop Science (AREA)
- Biochemistry (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB2520773A GB1409202A (en) | 1973-05-25 | 1973-05-25 | Fluorine-containing organo-phosphorus esters having pesticidal properties |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| IL44555A0 IL44555A0 (en) | 1974-06-30 |
| IL44555A true IL44555A (en) | 1977-01-31 |
Family
ID=10223960
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IL44555A IL44555A (en) | 1973-05-25 | 1974-04-03 | Pyrimidyl (thio)phosphoric acid esters |
Country Status (6)
| Country | Link |
|---|---|
| JP (1) | JPS5046841A (de) |
| CH (1) | CH585016A5 (de) |
| DE (1) | DE2425237A1 (de) |
| FR (1) | FR2230651B1 (de) |
| GB (1) | GB1409202A (de) |
| IL (1) | IL44555A (de) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3528264A1 (de) * | 1985-08-07 | 1987-02-12 | Bayer Ag | Phosphor(phosphon)-saeureester |
| DE3542173A1 (de) * | 1985-11-29 | 1987-06-04 | Basf Ag | Phosphorsaeurederivate, verfahren zu ihrer herstellung und ihre verwendung zur bekaempfung von schaedlingen |
| DE3914714A1 (de) * | 1989-05-04 | 1990-11-22 | Bayer Ag | Pyrimidinyl (thiono) (thiol)-phosphor(phosphon)saeure(amid)ester |
| DE19917785A1 (de) * | 1999-04-20 | 2000-10-26 | Bayer Ag | 2,4-Diamino-pyrimidin-Derivate |
-
1973
- 1973-05-25 GB GB2520773A patent/GB1409202A/en not_active Expired
-
1974
- 1974-04-03 IL IL44555A patent/IL44555A/en unknown
- 1974-05-21 JP JP49056199A patent/JPS5046841A/ja active Pending
- 1974-05-24 CH CH714374A patent/CH585016A5/xx not_active IP Right Cessation
- 1974-05-24 DE DE19742425237 patent/DE2425237A1/de active Pending
- 1974-05-24 FR FR7418098A patent/FR2230651B1/fr not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| DE2425237A1 (de) | 1974-12-12 |
| IL44555A0 (en) | 1974-06-30 |
| JPS5046841A (de) | 1975-04-25 |
| FR2230651B1 (de) | 1977-10-14 |
| FR2230651A1 (de) | 1974-12-20 |
| AU6937974A (en) | 1975-11-27 |
| GB1409202A (en) | 1975-10-08 |
| CH585016A5 (de) | 1977-02-28 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| PL84208B1 (de) | ||
| US3686200A (en) | Phosphoric acid esters | |
| US4041157A (en) | Fungicidal pyrimidine derivatives | |
| US3657247A (en) | Pesticidal halogen-substituted pyrimidinyl phosphorus esters | |
| US4014882A (en) | Trifluoromethyl substituted pyrimidine derivatives useful as insecticides | |
| US3629474A (en) | Insecticidal and fungicidal compositions and methods of combating fungi and insects using isoxazolyl carbamates | |
| IL44555A (en) | Pyrimidyl (thio)phosphoric acid esters | |
| US3932631A (en) | Certain organophosphorus compounds used to control insects | |
| US4237168A (en) | N-(4-Chloro-2-methylphenyl)-N-hydroxy methanimidamide and its pesticidal use | |
| CA1047497A (en) | Heterocyclic derivative | |
| US3767662A (en) | Certain 1,3-thiazolidin-4-ones | |
| US4225595A (en) | Piperazine phosphates and phosphonate insecticides | |
| GB2055103A (en) | 5-pyrimidinols and phosphorus esters thereof | |
| CH629084A5 (de) | Insektizide, akarizide und nematizide sowie verfahren zur herstellung neuer o-aethyl-s-n-propyl-0,2,2,2-trihalogen-aethylphosphorthiolate (oder -thionothiolate). | |
| US4048172A (en) | Carbonylmethylpyrimidin-6-yl phosphates and phosphorothionates | |
| US3325492A (en) | Thiophosphoric (-phosphonic, -phosphinic) or dithiophosphoric (-phosphonic, -phosphinic) acid esters | |
| US3935212A (en) | Pesticidal substituted 2-hydroxylaminopyrimidinyl phosphorus esters | |
| US4439430A (en) | O,O-Diethyl O-[(p-tertiarybutylthio)phenyl]phosphorothioates and its insecticidal use | |
| US3705914A (en) | Pesticidal carbamate derivatives of naphthaquinones | |
| US4424217A (en) | Substituted phenyl phosphorothioates and their use as pesticides | |
| DE69117310T2 (de) | Biphosphorylhydrazine und ihre Anwendung als Pestizide | |
| US3551562A (en) | Insecticidal use of s-((4-oxo-1,2,3-benzotriazin - 3(4h)-yl) - methyl) phosphorothioates and phosphorodithioates | |
| US3843655A (en) | Heterocyclic compounds and compositions | |
| US3151022A (en) | Omicron, omicron-dimethyl-omicron-(4-methylmercaptophenyl) phosphate and pesticidal use | |
| US3502670A (en) | S-((4-oxo - 1,2,3-benzotriazin-3(4h)-yl)-methyl) phosphorothioates and phosphorodithioates |