IL36583A - Thiophosphoric acid esters and their use as pesticides - Google Patents

Thiophosphoric acid esters and their use as pesticides

Info

Publication number: IL36583A
Authority: IL; Israel
Prior art keywords: compound; formula; active; weight; nematodes
Prior art date: 1970-04-30

Application number

IL36583A

Other languages

English (en)

Other versions

IL36583A0 (en

Original Assignee

Bayer Ag

Priority date (The priority date 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 date listed.)

1970-04-30

Filing date

1971-04-09

Publication date

1973-11-28

1971-04-09 Application filed by Bayer Ag filed Critical Bayer Ag

1971-06-23 Publication of IL36583A0 publication Critical patent/IL36583A0/xx

1973-11-28 Publication of IL36583A publication Critical patent/IL36583A/en

Links

239000000575 pesticide Substances 0.000 title description 2
150000003580 thiophosphoric acid esters Chemical class 0.000 title 1
150000001875 compounds Chemical class 0.000 claims description 79
239000000203 mixture Substances 0.000 claims description 19
238000000034 method Methods 0.000 claims description 15
239000003085 diluting agent Substances 0.000 claims description 13
241000244206 Nematoda Species 0.000 claims description 11
239000004480 active ingredient Substances 0.000 claims description 11
241000233866 Fungi Species 0.000 claims description 9
241000238631 Hexapoda Species 0.000 claims description 8
239000007788 liquid Substances 0.000 claims description 7
239000002253 acid Substances 0.000 claims description 6
239000007787 solid Substances 0.000 claims description 5
241001465754 Metazoa Species 0.000 claims description 4
125000000217 alkyl group Chemical group 0.000 claims description 4
230000000855 fungicidal effect Effects 0.000 claims description 4
125000004414 alkyl thio group Chemical group 0.000 claims description 3
230000000749 insecticidal effect Effects 0.000 claims description 3
125000004093 cyano group Chemical group *C#N 0.000 claims description 2
230000001069 nematicidal effect Effects 0.000 claims description 2
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 2
125000003545 alkoxy group Chemical group 0.000 claims 1
125000004644 alkyl sulfinyl group Chemical group 0.000 claims 1
229910052736 halogen Inorganic materials 0.000 claims 1
150000002367 halogens Chemical class 0.000 claims 1
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 1
244000045947 parasite Species 0.000 claims 1
239000004094 surface-active agent Substances 0.000 claims 1
-1 alkylsulphinyl radical Chemical class 0.000 description 8
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 6
WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 6
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
230000000694 effects Effects 0.000 description 6
238000002360 preparation method Methods 0.000 description 6
239000000243 solution Substances 0.000 description 6
238000006243 chemical reaction Methods 0.000 description 5
238000010998 test method Methods 0.000 description 5
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 4
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
241000607479 Yersinia pestis Species 0.000 description 4
239000013011 aqueous formulation Substances 0.000 description 4
235000013601 eggs Nutrition 0.000 description 4
239000003995 emulsifying agent Substances 0.000 description 4
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
241001556089 Nilaparvata lugens Species 0.000 description 3
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 3
235000012730 carminic acid Nutrition 0.000 description 3
238000004821 distillation Methods 0.000 description 3
238000009472 formulation Methods 0.000 description 3
229910052739 hydrogen Inorganic materials 0.000 description 3
239000001257 hydrogen Substances 0.000 description 3
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
239000011734 sodium Substances 0.000 description 3
229910052708 sodium Inorganic materials 0.000 description 3
239000002904 solvent Substances 0.000 description 3
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 2
241000255925 Diptera Species 0.000 description 2
241000196324 Embryophyta Species 0.000 description 2
MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
239000005909 Kieselgur Substances 0.000 description 2
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
240000007594 Oryza sativa Species 0.000 description 2
235000007164 Oryza sativa Nutrition 0.000 description 2
244000046052 Phaseolus vulgaris Species 0.000 description 2
235000010627 Phaseolus vulgaris Nutrition 0.000 description 2
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
241000256250 Spodoptera littoralis Species 0.000 description 2
239000002671 adjuvant Substances 0.000 description 2
229910052783 alkali metal Inorganic materials 0.000 description 2
150000001340 alkali metals Chemical class 0.000 description 2
229910000147 aluminium phosphate Inorganic materials 0.000 description 2
125000003118 aryl group Chemical group 0.000 description 2
229910052799 carbon Inorganic materials 0.000 description 2
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
229960001760 dimethyl sulfoxide Drugs 0.000 description 2
ZNOLGFHPUIJIMJ-UHFFFAOYSA-N fenitrothion Chemical compound COP(=S)(OC)OC1=CC=C([N+]([O-])=O)C(C)=C1 ZNOLGFHPUIJIMJ-UHFFFAOYSA-N 0.000 description 2
239000000417 fungicide Substances 0.000 description 2
230000001976 improved effect Effects 0.000 description 2
150000003254 radicals Chemical group 0.000 description 2
235000009566 rice Nutrition 0.000 description 2
229910000029 sodium carbonate Inorganic materials 0.000 description 2
238000003756 stirring Methods 0.000 description 2
NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 description 1
TVTJUIAKQFIXCE-HUKYDQBMSA-N 2-amino-9-[(2R,3S,4S,5R)-4-fluoro-3-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-7-prop-2-ynyl-1H-purine-6,8-dione Chemical compound NC=1NC(C=2N(C(N(C=2N=1)[C@@H]1O[C@@H]([C@H]([C@H]1O)F)CO)=O)CC#C)=O TVTJUIAKQFIXCE-HUKYDQBMSA-N 0.000 description 1
LJMGDHZXUKNDMC-UHFFFAOYSA-N 2-methylpropyl 3-dihydroxyphosphinothioylsulfanylpropanoate Chemical compound CC(C)COC(CCSP(O)(O)=S)=O LJMGDHZXUKNDMC-UHFFFAOYSA-N 0.000 description 1
241001143309 Acanthoscelides obtectus Species 0.000 description 1
241000238876 Acari Species 0.000 description 1
241001159389 Aculops pelekassi Species 0.000 description 1
241000175828 Adoxophyes orana Species 0.000 description 1
241000256118 Aedes aegypti Species 0.000 description 1
241001136265 Agriotes Species 0.000 description 1
239000005995 Aluminium silicate Substances 0.000 description 1
244000144730 Amygdalus persica Species 0.000 description 1
241000519878 Anomala rufocuprea Species 0.000 description 1
241001279740 Anopheles sinensis Species 0.000 description 1
241000134843 Aphelenchoides besseyi Species 0.000 description 1
241001095118 Aphis pomi Species 0.000 description 1
241000239290 Araneae Species 0.000 description 1
241000238657 Blattella germanica Species 0.000 description 1
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
241001313742 Callosobruchus chinensis Species 0.000 description 1
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
241000426497 Chilo suppressalis Species 0.000 description 1
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
241000207199 Citrus Species 0.000 description 1
241000254173 Coleoptera Species 0.000 description 1
241000144210 Culex pipiens pallens Species 0.000 description 1
241000256060 Culex tritaeniorhynchus Species 0.000 description 1
241000254171 Curculionidae Species 0.000 description 1
XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
206010011732 Cyst Diseases 0.000 description 1
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 1
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical class C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
241001466042 Fulgoromorpha Species 0.000 description 1
241000785585 Gryllotalpa africana Species 0.000 description 1
241000258937 Hemiptera Species 0.000 description 1
241000498254 Heterodera glycines Species 0.000 description 1
241000256602 Isoptera Species 0.000 description 1
241000721703 Lymantria dispar Species 0.000 description 1
241000255685 Malacosoma neustria Species 0.000 description 1
239000005949 Malathion Substances 0.000 description 1
241000243786 Meloidogyne incognita Species 0.000 description 1
241000257159 Musca domestica Species 0.000 description 1
241001615768 Musca domestica vicina Species 0.000 description 1
241000257226 Muscidae Species 0.000 description 1
241000721621 Myzus persicae Species 0.000 description 1
241000358422 Nephotettix cincticeps Species 0.000 description 1
241000819999 Nymphes Species 0.000 description 1
241000238814 Orthoptera Species 0.000 description 1
241000488581 Panonychus citri Species 0.000 description 1
241000238661 Periplaneta Species 0.000 description 1
241000255969 Pieris brassicae Species 0.000 description 1
241000227425 Pieris rapae crucivora Species 0.000 description 1
235000005805 Prunus cerasus Nutrition 0.000 description 1
235000006040 Prunus persica var persica Nutrition 0.000 description 1
241000596535 Pseudococcus comstocki Species 0.000 description 1
206010037660 Pyrexia Diseases 0.000 description 1
241000866500 Reticulitermes speratus Species 0.000 description 1
241000125162 Rhopalosiphum Species 0.000 description 1
241000254152 Sitophilus oryzae Species 0.000 description 1
KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 1
241000256248 Spodoptera Species 0.000 description 1
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
241001454293 Tetranychus urticae Species 0.000 description 1
244000269722 Thea sinensis Species 0.000 description 1
241000254113 Tribolium castaneum Species 0.000 description 1
241001630065 Unaspis yanonensis Species 0.000 description 1
BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical group ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical compound [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 description 1
229960000583 acetic acid Drugs 0.000 description 1
239000000853 adhesive Substances 0.000 description 1
230000001070 adhesive effect Effects 0.000 description 1
239000000443 aerosol Substances 0.000 description 1
239000003905 agrochemical Substances 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
125000002877 alkyl aryl group Chemical group 0.000 description 1
PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
235000012211 aluminium silicate Nutrition 0.000 description 1
125000000129 anionic group Chemical group 0.000 description 1
150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
JXLHNMVSKXFWAO-UHFFFAOYSA-N azane;7-fluoro-2,1,3-benzoxadiazole-4-sulfonic acid Chemical compound N.OS(=O)(=O)C1=CC=C(F)C2=NON=C12 JXLHNMVSKXFWAO-UHFFFAOYSA-N 0.000 description 1
230000003115 biocidal effect Effects 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
229910052794 bromium Inorganic materials 0.000 description 1
JYYOBHFYCIDXHH-UHFFFAOYSA-N carbonic acid;hydrate Chemical compound O.OC(O)=O JYYOBHFYCIDXHH-UHFFFAOYSA-N 0.000 description 1
239000000969 carrier Substances 0.000 description 1
235000020971 citrus fruits Nutrition 0.000 description 1
239000004927 clay Substances 0.000 description 1
239000007931 coated granule Substances 0.000 description 1
229940125851 compound 27 Drugs 0.000 description 1
208000031513 cyst Diseases 0.000 description 1
GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical compound O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 description 1
150000005690 diesters Chemical class 0.000 description 1
JXSJBGJIGXNWCI-UHFFFAOYSA-N diethyl 2-[(dimethoxyphosphorothioyl)thio]succinate Chemical compound CCOC(=O)CC(SP(=S)(OC)OC)C(=O)OCC JXSJBGJIGXNWCI-UHFFFAOYSA-N 0.000 description 1
GGSUCNLOZRCGPQ-UHFFFAOYSA-N diethylaniline Chemical compound CCN(CC)C1=CC=CC=C1 GGSUCNLOZRCGPQ-UHFFFAOYSA-N 0.000 description 1
125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
239000002270 dispersing agent Substances 0.000 description 1
239000003814 drug Substances 0.000 description 1
229940079593 drug Drugs 0.000 description 1
238000001035 drying Methods 0.000 description 1
244000078703 ectoparasite Species 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
238000011156 evaluation Methods 0.000 description 1
230000001747 exhibiting effect Effects 0.000 description 1
239000003337 fertilizer Substances 0.000 description 1
235000013312 flour Nutrition 0.000 description 1
239000012362 glacial acetic acid Substances 0.000 description 1
125000005843 halogen group Chemical group 0.000 description 1
125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
239000012442 inert solvent Substances 0.000 description 1
229910052740 iodine Inorganic materials 0.000 description 1
239000011630 iodine Substances 0.000 description 1
JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
ZLVXBBHTMQJRSX-VMGNSXQWSA-N jdtic Chemical group C1([C@]2(C)CCN(C[C@@H]2C)C[C@H](C(C)C)NC(=O)[C@@H]2NCC3=CC(O)=CC=C3C2)=CC=CC(O)=C1 ZLVXBBHTMQJRSX-VMGNSXQWSA-N 0.000 description 1
NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
229920005610 lignin Polymers 0.000 description 1
231100000053 low toxicity Toxicity 0.000 description 1
229960000453 malathion Drugs 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
SNVLJLYUUXKWOJ-UHFFFAOYSA-N methylidenecarbene Chemical compound C=[C] SNVLJLYUUXKWOJ-UHFFFAOYSA-N 0.000 description 1
239000002480 mineral oil Substances 0.000 description 1
235000010446 mineral oil Nutrition 0.000 description 1
238000002156 mixing Methods 0.000 description 1
229910052901 montmorillonite Inorganic materials 0.000 description 1
239000003921 oil Substances 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
230000003647 oxidation Effects 0.000 description 1
238000007254 oxidation reaction Methods 0.000 description 1
230000000590 parasiticidal effect Effects 0.000 description 1
239000002297 parasiticide Substances 0.000 description 1
239000002245 particle Substances 0.000 description 1
230000000361 pesticidal effect Effects 0.000 description 1
239000003208 petroleum Substances 0.000 description 1
150000003014 phosphoric acid esters Chemical class 0.000 description 1
239000003380 propellant Substances 0.000 description 1
FVSKHRXBFJPNKK-UHFFFAOYSA-N propionitrile Chemical compound CCC#N FVSKHRXBFJPNKK-UHFFFAOYSA-N 0.000 description 1
239000011541 reaction mixture Substances 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
159000000000 sodium salts Chemical class 0.000 description 1
KEAYESYHFKHZAL-BJUDXGSMSA-N sodium-22 Chemical compound [22Na] KEAYESYHFKHZAL-BJUDXGSMSA-N 0.000 description 1
238000005507 spraying Methods 0.000 description 1
LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 1
125000001174 sulfone group Chemical group 0.000 description 1
239000001117 sulphuric acid Substances 0.000 description 1
235000011149 sulphuric acid Nutrition 0.000 description 1
239000000725 suspension Substances 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
150000003512 tertiary amines Chemical class 0.000 description 1
150000007944 thiolates Chemical class 0.000 description 1
RYYWUUFWQRZTIU-UHFFFAOYSA-K thiophosphate Chemical compound [O-]P([O-])([O-])=S RYYWUUFWQRZTIU-UHFFFAOYSA-K 0.000 description 1
239000002699 waste material Substances 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
- A01N57/14—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds containing aromatic 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
- C07F9/06—Phosphorus compounds without P—C bonds
- C07F9/16—Esters of thiophosphoric acids or thiophosphorous acids
- C07F9/165—Esters of thiophosphoric acids
- C07F9/18—Esters of thiophosphoric acids with hydroxyaryl compounds

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)

IL36583A 1970-04-30 1971-04-09 Thiophosphoric acid esters and their use as pesticides IL36583A (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP45036305A JPS4916940B1 (de)	1970-04-30	1970-04-30

Publications (2)

Publication Number	Publication Date
IL36583A0 IL36583A0 (en)	1971-06-23
IL36583A true IL36583A (en)	1973-11-28

Family

ID=12466102

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
IL36583A IL36583A (en)	1970-04-30	1971-04-09	Thiophosphoric acid esters and their use as pesticides

Country Status (19)

Country	Link
US (1)	US3798292A (de)
JP (1)	JPS4916940B1 (de)
AT (1)	AT306437B (de)
BE (1)	BE766547A (de)
CA (1)	CA947649A (de)
CH (1)	CH548738A (de)
CS (1)	CS167312B2 (de)
DE (1)	DE2118495C3 (de)
DK (1)	DK131704C (de)
ES (1)	ES390733A1 (de)
FR (1)	FR2099083A5 (de)
GB (1)	GB1300192A (de)
HU (1)	HU162355B (de)
IL (1)	IL36583A (de)
NL (1)	NL7105929A (de)
PL (1)	PL76917B1 (de)
RO (1)	RO63329A (de)
SE (1)	SE381163B (de)
ZA (1)	ZA712444B (de)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3970728A (en) *	1971-10-21	1976-07-20	Bayer Aktiengesellschaft	O-Aryl-alkoxyethyl-thiolphosphoric acid ester
JPS5545526B2 (de) *	1972-04-06	1980-11-18
US4005197A (en) *	1972-04-06	1977-01-25	Bayer Aktiengesellschaft	Combating insects, acarids and nematodes with S-alkoxyethyl-phenyl-di- and tri-thiophosphonic acid esters

1970
- 1970-04-30 JP JP45036305A patent/JPS4916940B1/ja active Pending
1971
- 1971-04-09 IL IL36583A patent/IL36583A/en unknown
- 1971-04-16 ZA ZA712444A patent/ZA712444B/xx unknown
- 1971-04-16 DE DE2118495A patent/DE2118495C3/de not_active Expired
- 1971-04-16 CH CH560071A patent/CH548738A/de not_active IP Right Cessation
- 1971-04-21 GB GB00505/71A patent/GB1300192A/en not_active Expired
- 1971-04-22 SE SE7105262A patent/SE381163B/xx unknown
- 1971-04-22 US US00136584A patent/US3798292A/en not_active Expired - Lifetime
- 1971-04-27 CA CA111,436A patent/CA947649A/en not_active Expired
- 1971-04-28 RO RO7100066748A patent/RO63329A/ro unknown
- 1971-04-29 NL NL7105929A patent/NL7105929A/xx not_active Application Discontinuation
- 1971-04-29 HU HUBA2577A patent/HU162355B/hu unknown
- 1971-04-29 PL PL1971147846A patent/PL76917B1/pl unknown
- 1971-04-29 DK DK207671A patent/DK131704C/da active
- 1971-04-29 ES ES390733A patent/ES390733A1/es not_active Expired
- 1971-04-30 CS CS3166A patent/CS167312B2/cs unknown
- 1971-04-30 FR FR7115600A patent/FR2099083A5/fr not_active Expired
- 1971-04-30 BE BE766547A patent/BE766547A/xx unknown
- 1971-04-30 AT AT373571A patent/AT306437B/de not_active IP Right Cessation

Also Published As

Publication number	Publication date
FR2099083A5 (de)	1972-03-10
RO63329A (fr)	1978-07-15
ZA712444B (en)	1972-01-26
DE2118495C3 (de)	1979-10-31
DK131704B (da)	1975-08-25
IL36583A0 (en)	1971-06-23
DE2118495B2 (de)	1979-03-08
CH548738A (de)	1974-05-15
AT306437B (de)	1973-04-10
PL76917B1 (de)	1975-02-28
CA947649A (en)	1974-05-21
JPS4916940B1 (de)	1974-04-25
DE2118495A1 (de)	1971-12-02
ES390733A1 (es)	1974-11-16
CS167312B2 (de)	1976-04-29
BE766547A (fr)	1971-11-03
US3798292A (en)	1974-03-19
HU162355B (de)	1973-02-28
NL7105929A (de)	1971-11-02
DK131704C (da)	1976-01-26
SE381163B (sv)	1975-12-01
GB1300192A (en)	1972-12-20

Publication	Publication Date	Title
US4564611A (en)	1986-01-14	(Di)thio-phosphoric and -phosphonic acid derivatives, and their use in plant protection
US3839510A (en)	1974-10-01	O-ethyl-s,s-di-alkyl-phosphorothionodithiolates
US3763160A (en)	1973-10-02	Phosphorus containing esters of 2-hydroxyquinoxaline
US3670057A (en)	1972-06-13	S(alkllthio ethyl) phosphorothioamidate
US4303653A (en)	1981-12-01	Organic phosphoric acid ester derivatives, a process for preparing the same and insecticidal, miticidal or nematocidal compositions containing the same
IL36583A (en)	1973-11-28	Thiophosphoric acid esters and their use as pesticides
US3821246A (en)	1974-06-28	O-ethyl-s-alkyl-s-phthalimido-alkyl-phosphorodithiolates
US4387095A (en)	1983-06-07	Combating pests with O-Alkyl-S-alkyl-S-acyloxyethyl-phosphorodithiolates
US4443439A (en)	1984-04-17	Pesticidal phenylthionophosphonic acid esters
GB1560712A (en)	1980-02-06	Phosphoruscontaining isoxazole derivatives useful as pesticides
US3644598A (en)	1972-02-22	1 - alkoxy(-alkenyloxy -phenoxy) - 1-thiono-3-chloro(3-alkyl)phospholines
US4225595A (en)	1980-09-30	Piperazine phosphates and phosphonate insecticides
US4086239A (en)	1978-04-25	Thiazole bis-phosphates and phosphonates, intermediates, and insecticidal compositions and methods
US4028438A (en)	1977-06-07	Phosphorothiolates
US3763288A (en)	1973-10-02	O lower alkyl o substituted phenyl s alkoxyethylphosphorothiolates
US3880997A (en)	1975-04-29	Insecticidal and acaricidal phosphorous-containing esters of 2-hydroxyquinoxaline
US3894124A (en)	1975-07-08	S-alkoxyethyl-phenyl-di- and -tri- thiophosphonic acid esters
US4421750A (en)	1983-12-20	Organophosphoric acid ester anhydrides as pesticides
EP0116254B1 (de)	1986-10-15	Phenylthionophosphonsäureester
US4465675A (en)	1984-08-14	Insecticidal and fungicidal 1-alkyl-5-alkylsulfonyl-4-chloropyrazole-3-yl-(thio)phosphates and (thio)phosphonates
US4599329A (en)	1986-07-08	O,S-dialkyl S-[carbamyloxyalkyl] dithiophosphates and their use as pesticides
EP0068823B1 (de)	1988-05-04	Phosphoroamido(DI oder TRI)thioate-Derivate, sie enthaltende pestizide Zubereitungen und die Verwendung der neuen Derivaten als Schädlingsbekämpfungsmittel
US3755508A (en)	1973-08-28	S,s-di(2-alkoxy-ethyl)phosphoro- or phosphono-thionodithiolates
EP0054589B1 (de)	1984-10-17	Organische Phosphorsäureesterderivate, Verfahren zu ihrer Herstellung und sie enthaltende insektizide, mitizide oder nematozide Zubereitungen
US4005197A (en)	1977-01-25	Combating insects, acarids and nematodes with S-alkoxyethyl-phenyl-di- and tri-thiophosphonic acid esters