CH616687A5 - - Google Patents
Download PDFInfo
- Publication number
- CH616687A5 CH616687A5 CH1231475A CH1231475A CH616687A5 CH 616687 A5 CH616687 A5 CH 616687A5 CH 1231475 A CH1231475 A CH 1231475A CH 1231475 A CH1231475 A CH 1231475A CH 616687 A5 CH616687 A5 CH 616687A5
- Authority
- CH
- Switzerland
- Prior art keywords
- carbon atoms
- group
- formula
- alkyl group
- alkyl
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 claims description 35
- 125000004432 carbon atom Chemical group C* 0.000 claims description 31
- 125000000217 alkyl group Chemical group 0.000 claims description 18
- -1 bromo-substituted propylene Chemical group 0.000 claims description 16
- 239000000203 mixture Substances 0.000 claims description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 11
- 125000003342 alkenyl group Chemical group 0.000 claims description 10
- 239000004009 herbicide Substances 0.000 claims description 9
- 238000000034 method Methods 0.000 claims description 9
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims description 8
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 8
- 239000000460 chlorine Substances 0.000 claims description 6
- 239000008187 granular material Substances 0.000 claims description 6
- 239000002917 insecticide Substances 0.000 claims description 6
- 238000002360 preparation method Methods 0.000 claims description 6
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 5
- 239000002253 acid Substances 0.000 claims description 5
- 238000006243 chemical reaction Methods 0.000 claims description 5
- 229910052801 chlorine Inorganic materials 0.000 claims description 5
- 239000004495 emulsifiable concentrate Substances 0.000 claims description 5
- 150000003869 acetamides Chemical class 0.000 claims description 4
- 239000003795 chemical substances by application Substances 0.000 claims description 4
- 125000005843 halogen group Chemical group 0.000 claims description 4
- 230000001069 nematicidal effect Effects 0.000 claims description 4
- 239000004563 wettable powder Substances 0.000 claims description 4
- 241000251730 Chondrichthyes Species 0.000 claims description 3
- 150000001298 alcohols Chemical class 0.000 claims description 3
- 238000010410 dusting Methods 0.000 claims description 3
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 3
- 239000005645 nematicide Substances 0.000 claims description 3
- 239000002904 solvent Substances 0.000 claims description 3
- 229910052783 alkali metal Inorganic materials 0.000 claims description 2
- 150000001340 alkali metals Chemical class 0.000 claims description 2
- 125000003545 alkoxy group Chemical group 0.000 claims description 2
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 2
- 239000003337 fertilizer Substances 0.000 claims description 2
- 239000000417 fungicide Substances 0.000 claims description 2
- 150000002576 ketones Chemical class 0.000 claims description 2
- 239000000575 pesticide Substances 0.000 claims description 2
- 125000004429 atom Chemical group 0.000 claims 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 1
- 229910052794 bromium Chemical group 0.000 claims 1
- 125000001246 bromo group Chemical group Br* 0.000 claims 1
- 241000196324 Embryophyta Species 0.000 description 23
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 18
- 230000002363 herbicidal effect Effects 0.000 description 15
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 13
- 229910052700 potassium Inorganic materials 0.000 description 13
- 239000011591 potassium Substances 0.000 description 13
- 239000000243 solution Substances 0.000 description 9
- 240000007594 Oryza sativa Species 0.000 description 8
- 235000007164 Oryza sativa Nutrition 0.000 description 7
- 238000004519 manufacturing process Methods 0.000 description 7
- 235000009566 rice Nutrition 0.000 description 7
- 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 5
- 244000062793 Sorghum vulgare Species 0.000 description 5
- 235000019713 millet Nutrition 0.000 description 5
- 229910052708 sodium Inorganic materials 0.000 description 5
- 239000011734 sodium Substances 0.000 description 5
- 238000011282 treatment Methods 0.000 description 5
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- 240000006122 Chenopodium album Species 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- 241000238631 Hexapoda Species 0.000 description 4
- 235000003990 Monochoria hastata Nutrition 0.000 description 4
- 231100000674 Phytotoxicity Toxicity 0.000 description 4
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
- 230000000895 acaricidal effect Effects 0.000 description 4
- 239000004927 clay Substances 0.000 description 4
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 4
- 235000019441 ethanol Nutrition 0.000 description 4
- 230000000749 insecticidal effect Effects 0.000 description 4
- 238000010298 pulverizing process Methods 0.000 description 4
- 239000004094 surface-active agent Substances 0.000 description 4
- 244000058871 Echinochloa crus-galli Species 0.000 description 3
- 241000255777 Lepidoptera Species 0.000 description 3
- 241000169139 Monochoria Species 0.000 description 3
- 241000244206 Nematoda Species 0.000 description 3
- 235000011999 Panicum crusgalli Nutrition 0.000 description 3
- 244000234609 Portulaca oleracea Species 0.000 description 3
- 235000001855 Portulaca oleracea Nutrition 0.000 description 3
- 244000088415 Raphanus sativus Species 0.000 description 3
- 235000006140 Raphanus sativus var sativus Nutrition 0.000 description 3
- 239000004480 active ingredient Substances 0.000 description 3
- NAGJZTKCGNOGPW-UHFFFAOYSA-N dithiophosphoric acid Chemical class OP(O)(S)=S NAGJZTKCGNOGPW-UHFFFAOYSA-N 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 238000000921 elemental analysis Methods 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 239000000454 talc Substances 0.000 description 3
- 229910052623 talc Inorganic materials 0.000 description 3
- QPUYECUOLPXSFR-UHFFFAOYSA-N 1-methylnaphthalene Chemical compound C1=CC=C2C(C)=CC=CC2=C1 QPUYECUOLPXSFR-UHFFFAOYSA-N 0.000 description 2
- 235000005474 African couch grass Nutrition 0.000 description 2
- 241000218473 Agrotis Species 0.000 description 2
- 240000001592 Amaranthus caudatus Species 0.000 description 2
- 235000009328 Amaranthus caudatus Nutrition 0.000 description 2
- 244000237956 Amaranthus retroflexus Species 0.000 description 2
- 235000013479 Amaranthus retroflexus Nutrition 0.000 description 2
- 235000009344 Chenopodium album Nutrition 0.000 description 2
- 235000011498 Chenopodium album var missouriense Nutrition 0.000 description 2
- 235000013328 Chenopodium album var. album Nutrition 0.000 description 2
- 235000014052 Chenopodium album var. microphyllum Nutrition 0.000 description 2
- 235000014050 Chenopodium album var. stevensii Nutrition 0.000 description 2
- 235000013012 Chenopodium album var. striatum Nutrition 0.000 description 2
- 241000254173 Coleoptera Species 0.000 description 2
- 244000152970 Digitaria sanguinalis Species 0.000 description 2
- 235000010823 Digitaria sanguinalis Nutrition 0.000 description 2
- 241001520106 Eustachys Species 0.000 description 2
- 241000287828 Gallus gallus Species 0.000 description 2
- 241001477931 Mythimna unipuncta Species 0.000 description 2
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
- 244000155504 Rotala indica Species 0.000 description 2
- 244000173853 Sanguisorba officinalis Species 0.000 description 2
- 241001454295 Tetranychidae Species 0.000 description 2
- 235000012735 amaranth Nutrition 0.000 description 2
- 239000004178 amaranth Substances 0.000 description 2
- 239000000440 bentonite Substances 0.000 description 2
- 229910000278 bentonite Inorganic materials 0.000 description 2
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 2
- 235000013339 cereals Nutrition 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 230000001665 lethal effect Effects 0.000 description 2
- 230000002688 persistence Effects 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- 229910000029 sodium carbonate Inorganic materials 0.000 description 2
- 229920005552 sodium lignosulfonate Polymers 0.000 description 2
- 239000002689 soil Substances 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- MEKOFIRRDATTAG-UHFFFAOYSA-N 2,2,5,8-tetramethyl-3,4-dihydrochromen-6-ol Chemical compound C1CC(C)(C)OC2=C1C(C)=C(O)C=C2C MEKOFIRRDATTAG-UHFFFAOYSA-N 0.000 description 1
- IHCCLXNEEPMSIO-UHFFFAOYSA-N 2-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]piperidin-1-yl]-1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethanone Chemical group C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C1CCN(CC1)CC(=O)N1CC2=C(CC1)NN=N2 IHCCLXNEEPMSIO-UHFFFAOYSA-N 0.000 description 1
- 241000238876 Acari Species 0.000 description 1
- 235000006760 Acer pensylvanicum Nutrition 0.000 description 1
- 241000743985 Alopecurus Species 0.000 description 1
- 241000189413 Alopecurus geniculatus Species 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- 241001124076 Aphididae Species 0.000 description 1
- 241000219310 Beta vulgaris subsp. vulgaris Species 0.000 description 1
- 241001674044 Blattodea 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
- 241001313742 Callosobruchus chinensis Species 0.000 description 1
- 244000025254 Cannabis sativa Species 0.000 description 1
- 241000219312 Chenopodium Species 0.000 description 1
- 101100351213 Chromobacterium violaceum (strain ATCC 12472 / DSM 30191 / JCM 1249 / NBRC 12614 / NCIMB 9131 / NCTC 9757) pcp gene Proteins 0.000 description 1
- 229940126062 Compound A Drugs 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- 241000234653 Cyperus Species 0.000 description 1
- 241000759199 Eleocharis acicularis Species 0.000 description 1
- 235000007351 Eleusine Nutrition 0.000 description 1
- 241000209215 Eleusine Species 0.000 description 1
- 244000025670 Eleusine indica Species 0.000 description 1
- 235000014716 Eleusine indica Nutrition 0.000 description 1
- 244000068988 Glycine max Species 0.000 description 1
- 235000010469 Glycine max Nutrition 0.000 description 1
- 244000299507 Gossypium hirsutum Species 0.000 description 1
- NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 description 1
- 101000873111 Homo sapiens Vesicle transport protein SEC20 Proteins 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- 240000008415 Lactuca sativa Species 0.000 description 1
- 235000003228 Lactuca sativa Nutrition 0.000 description 1
- 235000007688 Lycopersicon esculentum Nutrition 0.000 description 1
- 241001490213 Milium Species 0.000 description 1
- 235000005052 Milium effusum Nutrition 0.000 description 1
- 240000000178 Monochoria vaginalis Species 0.000 description 1
- 241000257226 Muscidae Species 0.000 description 1
- 241000341511 Nematodes Species 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 240000007019 Oxalis corniculata Species 0.000 description 1
- 235000016499 Oxalis corniculata Nutrition 0.000 description 1
- 235000006089 Phaseolus angularis Nutrition 0.000 description 1
- 241000907661 Pieris rapae Species 0.000 description 1
- 240000004713 Pisum sativum Species 0.000 description 1
- 235000010582 Pisum sativum Nutrition 0.000 description 1
- 244000292693 Poa annua Species 0.000 description 1
- 241000209504 Poaceae Species 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 241000219295 Portulaca Species 0.000 description 1
- 241001370065 Portulaca oleracea subsp. sativa Species 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- PXIPVTKHYLBLMZ-UHFFFAOYSA-N Sodium azide Chemical compound [Na+].[N-]=[N+]=[N-] PXIPVTKHYLBLMZ-UHFFFAOYSA-N 0.000 description 1
- 240000003768 Solanum lycopersicum Species 0.000 description 1
- 235000021536 Sugar beet Nutrition 0.000 description 1
- 241001454293 Tetranychus urticae Species 0.000 description 1
- 235000021307 Triticum Nutrition 0.000 description 1
- 244000098338 Triticum aestivum Species 0.000 description 1
- 102100035030 Vesicle transport protein SEC20 Human genes 0.000 description 1
- 240000007098 Vigna angularis Species 0.000 description 1
- 235000010711 Vigna angularis Nutrition 0.000 description 1
- 240000008042 Zea mays Species 0.000 description 1
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 1
- 239000000642 acaricide Substances 0.000 description 1
- 239000003905 agrochemical Substances 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
- 239000000920 calcium hydroxide Substances 0.000 description 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 238000004440 column chromatography Methods 0.000 description 1
- 235000005822 corn Nutrition 0.000 description 1
- 244000038559 crop plants Species 0.000 description 1
- 230000002498 deadly effect Effects 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 239000005337 ground glass Substances 0.000 description 1
- 230000012447 hatching Effects 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
- 230000002147 killing effect Effects 0.000 description 1
- 239000012669 liquid formulation Substances 0.000 description 1
- 230000000813 microbial effect Effects 0.000 description 1
- PJFGPJQBWSEWKX-UHFFFAOYSA-N n-[(2,4-dichlorophenoxy)-methoxyphosphinothioyl]propan-2-amine Chemical compound CC(C)NP(=S)(OC)OC1=CC=C(Cl)C=C1Cl PJFGPJQBWSEWKX-UHFFFAOYSA-N 0.000 description 1
- 239000002420 orchard Substances 0.000 description 1
- 101150075058 pcp1 gene Proteins 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 239000002728 pyrethroid Substances 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000009331 sowing Methods 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000001308 synthesis method Methods 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 239000010455 vermiculite Substances 0.000 description 1
- 229910052902 vermiculite Inorganic materials 0.000 description 1
- 235000019354 vermiculite Nutrition 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 239000008096 xylene 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
- C07F9/1651—Esters of thiophosphoric acids with hydroxyalkyl compounds with further substituents on alkyl
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)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP49110264A JPS5154929A (en) | 1974-09-24 | 1974-09-24 | Shinkinajoso satsuchu satsudani satsusenchusoseibutsu oyobisono seizoho |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH616687A5 true CH616687A5 (es) | 1980-04-15 |
Family
ID=14531269
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH1231475A CH616687A5 (es) | 1974-09-24 | 1975-09-23 |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US4023956A (es) |
| JP (1) | JPS5154929A (es) |
| CA (1) | CA1039299A (es) |
| CH (1) | CH616687A5 (es) |
| ES (1) | ES441183A1 (es) |
| FR (1) | FR2286144A1 (es) |
| GB (1) | GB1484790A (es) |
| IT (1) | IT1047306B (es) |
| MX (1) | MX3630E (es) |
| NL (1) | NL7511191A (es) |
| SU (1) | SU701518A3 (es) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0037377A1 (de) * | 1980-03-27 | 1981-10-07 | Ciba-Geigy Ag | Metallkomplexfarbstoffe, deren Herstellung und Verwendung |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2604224A1 (de) * | 1976-02-04 | 1977-08-11 | Hoechst Ag | Herbizide mittel |
| JPS5517322A (en) * | 1978-07-21 | 1980-02-06 | Sumitomo Chem Co Ltd | Thiophosphoric acid ester derivative, its preparation, and insecticide, miticide, nematocide and fungicide containing the same |
| JPS5829955B2 (ja) * | 1979-06-14 | 1983-06-25 | 住友化学工業株式会社 | チオリン酸エステル誘導体およびその製造法 |
| JPS57130468U (es) * | 1981-02-10 | 1982-08-14 | ||
| US4528140A (en) * | 1983-07-08 | 1985-07-09 | The Procter & Gamble Company | Synthesis of alpha-dithiophosphato amides |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3102019A (en) * | 1961-08-16 | 1963-08-27 | Monsanto Chemicals | Method for inhibiting germination and preemergent growth of plants using s(n-aryl, n-aliphatic carbamoylmethyl) phosphorothiate triesters |
| US3385689A (en) * | 1965-10-11 | 1968-05-28 | Velsicol Chemical Corp | Method of controlling undesirable plant growth |
| JPS5527882B1 (es) * | 1970-05-13 | 1980-07-24 | ||
| BE793210A (fr) * | 1971-12-24 | 1973-06-22 | Ciba Geigy | Esters d'acides thiophosphoriques utilisables notamment comme matieres actives de produits phytopharmaceutiques |
-
1974
- 1974-09-24 JP JP49110264A patent/JPS5154929A/ja active Granted
-
1975
- 1975-09-09 US US05/611,606 patent/US4023956A/en not_active Expired - Lifetime
- 1975-09-22 MX MX752805U patent/MX3630E/es unknown
- 1975-09-23 GB GB39033/75A patent/GB1484790A/en not_active Expired
- 1975-09-23 FR FR7529162A patent/FR2286144A1/fr active Granted
- 1975-09-23 CA CA236,139A patent/CA1039299A/en not_active Expired
- 1975-09-23 ES ES441183A patent/ES441183A1/es not_active Expired
- 1975-09-23 CH CH1231475A patent/CH616687A5/de not_active IP Right Cessation
- 1975-09-23 NL NL7511191A patent/NL7511191A/xx not_active Application Discontinuation
- 1975-09-23 SU SU752174202A patent/SU701518A3/ru active
- 1975-09-24 IT IT69373/75A patent/IT1047306B/it active
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0037377A1 (de) * | 1980-03-27 | 1981-10-07 | Ciba-Geigy Ag | Metallkomplexfarbstoffe, deren Herstellung und Verwendung |
Also Published As
| Publication number | Publication date |
|---|---|
| NL7511191A (nl) | 1976-03-26 |
| ES441183A1 (es) | 1977-03-16 |
| GB1484790A (en) | 1977-09-08 |
| FR2286144A1 (fr) | 1976-04-23 |
| DE2542193B2 (de) | 1977-01-27 |
| MX3630E (es) | 1981-04-07 |
| JPS5335133B2 (es) | 1978-09-26 |
| US4023956A (en) | 1977-05-17 |
| IT1047306B (it) | 1980-09-10 |
| FR2286144B1 (es) | 1978-04-07 |
| SU701518A3 (ru) | 1979-11-30 |
| JPS5154929A (en) | 1976-05-14 |
| CA1039299A (en) | 1978-09-26 |
| DE2542193A1 (de) | 1976-04-15 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DD273768A5 (de) | Pflanzenwachstums-regulatorzusammensetzung | |
| CH621921A5 (es) | ||
| DE2212268B2 (de) | N-Halogenacetylanilinoessigsäureester, Verfahren zu deren Herstellung und diese enthaltende herbicide Massen | |
| DE3146309A1 (de) | Substituierte 2-/1-(oxyamino)-alkyliden/-cyclohexan-1,3-dione, diese enthaltende herbizide mittel und verfahren zum abtoeten einer vegetation | |
| DE2905650C2 (es) | ||
| CH666890A5 (de) | 2-(1-(3-chlorallyloxyamino)-alkyliden)-5-alkylthioalkyl-cyclohexan-1,3-dion. | |
| CH636600A5 (de) | 2-hydroxybenzamidderivate und verwendung derselben als fungizide. | |
| CH616687A5 (es) | ||
| EP0007089B1 (de) | Acylanilide mit herbicider und fungicider Wirkung, Verfahren zu ihrer Herstellung und ihre Verwendung | |
| EP0233151B1 (de) | Ester als Herbizide | |
| CH631721A5 (de) | Pflanzenschutzmittel. | |
| DE1518687A1 (de) | Neue Phosphorcarbonylverbindungen und solche enthaltende Mittel | |
| DE2952483C2 (de) | O-Sulfamoylglykolsäureamid-Derivate und deren Verwendung in einem herbiziden Mittel | |
| DE3300056C2 (de) | 3-Nitrobenzolsulfonanilid-Derivate und diese enthaltende fungizide Mittel | |
| DE2636620A1 (de) | Herbicide, keimtoetende und acarizide mittel | |
| DE2112643B2 (de) | Formanüdin-Denvate und sie enthaltende Mittel | |
| DE2361189A1 (de) | Oximino-thiolphosphorsaeureester, verfahren zu deren herstellung und deren verwendung als pestizide | |
| DE3546928C2 (de) | Verwendung von Trans-2-[1-(3-chlorallyloxyamino)propyliden]-5-(2-ethylthiopropyl)cyclohexan-1,3-dion in herbiziden Mitteln | |
| DE2201668A1 (de) | Neue Carboxanilide,ihre Herstellung und Verwendung | |
| DE2260763A1 (de) | Mittel zum abtoeten von schaedlichen organismen | |
| DE2119211A1 (en) | Organophosphates - active against insects and nematodes | |
| AT368681B (de) | Herbizide zusammensetzungen | |
| AT398074B (de) | Verfahren zur herstellung des neuen 2-(1-(3-trans-chlorallyoxyamino)-propyliden)-5- 2- ethylthiopropyl)-cyclohexan-1,3-dions | |
| DE2362333A1 (de) | Phosphororganische herbizide | |
| RU2060988C1 (ru) | Замещенное производное бициклогептандиона и гербицидная композиция |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PL | Patent ceased |