PL89163B1 - - Google Patents
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- PL89163B1 PL89163B1 PL1973161904A PL16190473A PL89163B1 PL 89163 B1 PL89163 B1 PL 89163B1 PL 1973161904 A PL1973161904 A PL 1973161904A PL 16190473 A PL16190473 A PL 16190473A PL 89163 B1 PL89163 B1 PL 89163B1
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- Poland
- Prior art keywords
- ethyl
- radical
- carbon atoms
- phenyl
- formula
- Prior art date
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- 239000000203 mixture Substances 0.000 claims description 10
- -1 alkynyl radical Chemical class 0.000 claims description 8
- 230000002363 herbicidal effect Effects 0.000 claims description 7
- 125000004432 carbon atom Chemical group C* 0.000 claims description 6
- 239000004009 herbicide Substances 0.000 claims description 4
- 125000000217 alkyl group Chemical group 0.000 claims description 3
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 2
- HNUALPPJLMYHDK-UHFFFAOYSA-N C[CH]C Chemical compound C[CH]C HNUALPPJLMYHDK-UHFFFAOYSA-N 0.000 claims description 2
- GNVMUORYQLCPJZ-UHFFFAOYSA-M Thiocarbamate Chemical compound NC([S-])=O GNVMUORYQLCPJZ-UHFFFAOYSA-M 0.000 claims description 2
- YUDRVAHLXDBKSR-UHFFFAOYSA-N [CH]1CCCCC1 Chemical group [CH]1CCCCC1 YUDRVAHLXDBKSR-UHFFFAOYSA-N 0.000 claims description 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 2
- 229910052794 bromium Chemical group 0.000 claims description 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
- 239000000460 chlorine Substances 0.000 claims description 2
- 229910052801 chlorine Inorganic materials 0.000 claims description 2
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 2
- 239000004480 active ingredient Substances 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 claims 1
- 150000003254 radicals Chemical class 0.000 claims 1
- 239000013543 active substance Substances 0.000 description 10
- 240000008042 Zea mays Species 0.000 description 8
- 235000008427 Brassica arvensis Nutrition 0.000 description 6
- 244000024671 Brassica kaber Species 0.000 description 6
- 235000004977 Brassica sinapistrum Nutrition 0.000 description 6
- 235000007244 Zea mays Nutrition 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 241001148727 Bromus tectorum Species 0.000 description 5
- 241000196324 Embryophyta Species 0.000 description 5
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 5
- 241000335053 Beta vulgaris Species 0.000 description 4
- 241000219312 Chenopodium Species 0.000 description 4
- 244000042664 Matricaria chamomilla Species 0.000 description 4
- 235000007232 Matricaria chamomilla Nutrition 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- 230000006378 damage Effects 0.000 description 4
- 239000003921 oil Substances 0.000 description 4
- 235000021533 Beta vulgaris Nutrition 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 244000056139 Brassica cretica Species 0.000 description 2
- 235000003351 Brassica cretica Nutrition 0.000 description 2
- 235000003343 Brassica rupestris Nutrition 0.000 description 2
- 240000006122 Chenopodium album Species 0.000 description 2
- 235000009344 Chenopodium album Nutrition 0.000 description 2
- 240000006162 Chenopodium quinoa Species 0.000 description 2
- 241000192043 Echinochloa Species 0.000 description 2
- 241000209082 Lolium Species 0.000 description 2
- 240000004296 Lolium perenne Species 0.000 description 2
- 235000017945 Matricaria Nutrition 0.000 description 2
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 2
- QKSKPIVNLNLAAV-UHFFFAOYSA-N bis(2-chloroethyl) sulfide Chemical compound ClCCSCCCl QKSKPIVNLNLAAV-UHFFFAOYSA-N 0.000 description 2
- 239000004927 clay Substances 0.000 description 2
- 239000012141 concentrate Substances 0.000 description 2
- 239000003337 fertilizer Substances 0.000 description 2
- 239000008187 granular material Substances 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 235000010460 mustard Nutrition 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- 241000743985 Alopecurus Species 0.000 description 1
- 241001621841 Alopecurus myosuroides Species 0.000 description 1
- 235000021537 Beetroot Nutrition 0.000 description 1
- 235000016068 Berberis vulgaris Nutrition 0.000 description 1
- 241000209200 Bromus Species 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 235000007866 Chamaemelum nobile Nutrition 0.000 description 1
- 244000058871 Echinochloa crus-galli Species 0.000 description 1
- LDLWBQFQYRXFOO-UHFFFAOYSA-N NC=1C(NN=CC1Br)=O Chemical compound NC=1C(NN=CC1Br)=O LDLWBQFQYRXFOO-UHFFFAOYSA-N 0.000 description 1
- 235000011999 Panicum crusgalli Nutrition 0.000 description 1
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
- 235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 description 1
- 241001148683 Zostera marina Species 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 239000011280 coal tar Substances 0.000 description 1
- 235000005822 corn Nutrition 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- 239000002283 diesel fuel Substances 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- CUANDTPGVLGJLG-UHFFFAOYSA-N heptylcarbamothioic s-acid Chemical compound CCCCCCCNC(S)=O CUANDTPGVLGJLG-UHFFFAOYSA-N 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000003350 kerosene Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 235000009973 maize Nutrition 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 150000002790 naphthalenes Chemical class 0.000 description 1
- HEAHCDNRFZZQOC-UHFFFAOYSA-N o-ethyl n-cyclohexyl-n-ethylcarbamothioate Chemical compound CCOC(=S)N(CC)C1CCCCC1 HEAHCDNRFZZQOC-UHFFFAOYSA-N 0.000 description 1
- 239000012053 oil suspension Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- DCKVNWZUADLDEH-UHFFFAOYSA-N sec-butyl acetate Chemical group CCC(C)OC(C)=O DCKVNWZUADLDEH-UHFFFAOYSA-N 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 description 1
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 1
- WJCNZQLZVWNLKY-UHFFFAOYSA-N thiabendazole Chemical compound S1C=NC(C=2NC3=CC=CC=C3N=2)=C1 WJCNZQLZVWNLKY-UHFFFAOYSA-N 0.000 description 1
- 150000003558 thiocarbamic acid derivatives Chemical class 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000000080 wetting agent 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/58—1,2-Diazines; Hydrogenated 1,2-diazines
-
- 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
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/32—Ingredients for reducing the noxious effect of the active substances to organisms other than pests, e.g. toxicity reducing compositions, self-destructing compositions
-
- 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
-
- 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/80—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,2
-
- 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/90—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system
-
- 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/12—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing a —O—CO—N< group, or a thio analogue thereof, neither directly attached to a ring nor the nitrogen atom being a member of a heterocyclic ring
-
- 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
- A01N2300/00—Combinations or mixtures of active ingredients covered by classes A01N27/00 - A01N65/48 with other active or formulation relevant ingredients, e.g. specific carrier materials or surfactants, covered by classes A01N25/00 - A01N65/48
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Dentistry (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Toxicology (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Description
Przedmiotem wynalazku jest srodek chwastobójczy. Znane jest stosowanie tiokarbaminianów i pirydazo- nów do zwalczania chwastów i chwastów trawiastych. Ich dzialanie herbicydowe jest jednak slabe.Stwierdzono, ze mieszanina skladajaca sie z tiokarbaminianu o wzorze 1, w którym Rx oznacza nizszy rodnik alkilowy lub alkinylowy zawierajacy do 4 atomów wegla, R2 oznacza rodnik cykloheksylowy, dwu- lub trójcykloalifatyczny rodnik weglowodorowy zawierajacy do 8 atomów wegla i R3 oznacza rodnik alkilowy zawierajacy do 4 atomów wegla, zwiazku o wzorze 2, w którym Y oznacza atom chloru lub bromu i X oznacza grupe o wzorze -NH-CHOH-CCI3 lub o wzorze NH-CO-COO-R, w którym R oznacza trzeciorzedowy rodnik butylowy lub izopropylowy, ma lepsze wlasciwosci chwastobójcze.Substancje czynne mozna stosowac w dowolnych stosunkach wagowych. Korzystnymi stosunkami wago¬ wymi poszczególnych skladników wynosza 1:5 do 5:1, korzystnie 3:1 do 1:3.Nowy srodek chwastobójczy wedlug wynalazku mozna stosowac w postaci roztworów, emulsji, zawiesin, zawiesin olejowych, proszków do opylania i granulatów. Postacie robocze zaleza calkowicie od celów stosowania.W kazdym przypadku do wytworzenia roztworów do bezposredniego opryskiwania stosuje sie frakcje olejów mineralnych o sredniej do wysokiej temperatury wrzenia, nafte lub olej napedowy, dalej oleje smoly weglowej, oleje pochodzenia roslinnego i zwierzecego, ponadto cykliczne weglowodory takie jak czterowodoronaftalen i alkilowane naftaleny.Wodne preparaty robocze mozna przygotowac z koncentratów emulsji, past lub proszków zwilzalnych przez dodanie wody. W celu otrzymania emulsji same substancje czynne lub rozpuszczone w wodzie emulguje sie w wodzie przy uzyciu substancji zwilzalnych lub dyspergujacych. Mozna tez otrzymywac koncentraty skladajace sie z substancji czynnej, substancji zwilzajacych, przyczepnych, emulgujacych lub dyspergujacych i ewentualnie rozpuszczalnikówi nastepnie rozcienczac woda.Do gotowych cieczy do opryskiwania mozna wprowadzac oleje róznych typów.Proszki do opylania mozna otrzymac przez zmieszanie lub wspólne zmielenie sbstancji czynnych ze stalym nosnikiem, na przyklad glina lub nawozami sztucznymi.2 89163 Granulaty mozna otrzymac przez zwiazanie substancji czynnych na nosnikach. Oprócz tego stosujac oleje mozna otrzymac zawiesiny do bezposredniego oprykiwania.Nowe substancje czynne mozna mieszac z nawozami, insektycydami, fungicydami lub innymi herbicydami.Przyklad I. W szklarni wypelnia sie gliniastym piaskiem naczynia doswiadczalne i wysiewa sie w nich nasiona buraków (Beta yulgaris), kukurydzy (Zea mays), gorczycy (Sinapis arvensis), komosy bialej (Chenopo¬ dium album), chwastnicy jednostronnej (Echinochloa crus galli), rajgrasu angielskiego (Lolium perenna), stoklosy (Bromus tectorum). Nastepnie glebe traktuje sie nizej podanymi pojedynczymi substancjami lub ich mieszanina¬ mi zdyspergowanymi lub zemulgowanymi w 500 litrach wody: I N-etylo-N-dwucyklo-[ 2,2,1 ]-heptylotiokarbaminian etylu w ilosci 1,5 i 3 kg/ha II estrem etylowym kwasu N-etylo-N-cykloheksylotiokarbaminowego w ilosci 1,5 i 4 kg/ha, III l-fenylo-4-/ a-hydroksy- j8,0,0-trójchloroetylo/ amino-5-bromopirydazonem-/6/ w ilosci l ,5 i 4 kg/ha, IV estrem izopropylowym kwasu N-[ l-fenylo-5-bromopirydazon-/6/-ylo-/4/ ] oksaminowego w ilosci 2,5 i 4 kg/ha I + III w ilosci 1,5 + 1,5 kg/ha II + IV w ilosci 1,5 + 2,5 kg/ha Z wyników prób zestawionych w tablicach I i II wynika, ze mieszaniny I+III i II+IV w porównaniu z po¬ szczególnymi skladnikami I-IV maja lepsze dzialanie chwastobójcze i lepiej sa tolerowane przez rosliny uprawne.TablicaI Roslina Beta vulgaris Zea mays Sinapis arvensis Chenopodium alb.Echinochloa c-g.Lolium perenne Bromus tectorum Substancja czynna kg/ha I 1.5 0 0 60 60 45 3 45 85 90 70 II 1,5 0 0 60 75 40 4 95 100 90 III | 1,5 0 0 55 60 3 | 100 100 75 80 70 Tablica II Roslina Beta vulgaris Zea mays Sinapis arvensis Chenopodium alb.Echinochloa c.-g.Lolium perenna Bromustectorum Substancja czynna w kg/ha IV 2,5 0 50 45 4 85 85 70 50 60 I + III 1,5+1,5 o o o o o o o 1 o o o o o II + IV | 1,5+2,5 0 100 95 100 100 95 0 = bez uszkodzen 100 = calkowite zniszczenie rosliny Przyklad II. Rosliny takie jak buraki (Beta vulgaris), kukurydza (Zea mays), gorczyca (Sinapis arven- sis), komosa biala (Chenopodium album), rumianek pospolity (Matricaria chamomilla), stoklosa (Bromus tecto¬ rum) i wyczyniec polny (Alopecurus myosuroides) o wysokosci 4-18 cm rosnace w szklarni traktuje sie poszcze¬ gólnymi substancjami czynnymi lub ich mieszaninami w kg/ha zemulgowanymi kazdorazowo w 5001 wody.I N-etylo-N-dwucyklo-[ 2,2,1 ]-heptylotiokarbaminianem etylu w ilosci 1,2 i 3 kg/ha II l-fenylo-4-/ a -hydroksy- 0,0, 0-trójchloroetyloamino/ -5-bromopirydazonem- /6/ w ilosci 2 i 3 kg/ha I+11 w ilosci 1+2 kg/ha Z nizej podanych tablic III i IV wynika, ze mieszaniny I + II maja lepsze dzialanie chwastobójcze niz poszczególne skladniki mieszaniny i jednoczesnie sa lepiej tolerowane przez rosliny uprawne.89163 Tablica III Roslina Beta yulgaris Zea mays Sinapis arvensis Chenopodium alb.Matricaria chamom.Bromustectorum Alo pecum s myo sur.Substancja czynna kg/ha I 1 0 0 2 0 0 65 65 3 0 85 90 Tablica TV Roslina Beta yulgaris Zea mays Sinapis arvensis Chenopodium alb.Matricaria cliamom.Bromustectorum Alopecurus myosur.Substancja czynna kg/ha 1 II 2 0 70 75 70 40 40 3 100 100 100 70 70 I+ 11 1 + 2 0 95 100 95 95 95 0 = brak uszkodzen 100 = calkowite zniszczenie rosliny Nizej podane mieszaniny sa podobnie skuteczne jak mieszaniny opisane w przykladzie I.N-etylo-N-dwucyklo- [ 2,2,1 ]-heptylotiokarbaminian etylu i ester izopropylowo-III-rzed.butylowy kwasu N-[ l-fenylo-5-bromopirydazon- /6/ -ylo-/4/]-oksaminowego. N-l- lub 2-dwucyklo-[ 3,3,0 ]-oktylo-N-etylotio- karbaminian etylu, lub l-fenylo-4-/ a-hydroksy-0,0, /3-trójchloroetylo/-amino-5-bromopirydazon- /6/, lub N-l- lub 2-dwucyklo-[ 3,3,0 ]-oktylo-N-etylotiokarbaminian etylu, lub ester izopropylowy kwasu N-[ l-fenylo-5-bromo- pirydazon-/6/-/ 4/]-oksaminowego, lub N-etylo-N-dwucyklo-[ 2,2,1 ]-heptylotiokarbaminian etylu i 1-fenylo-4-/a^ -hydroksytrqchloroetyloamino-5-chloropirydazon-/6/. Ester S-etlowy kwasu N-[l lub 2-/3a,4,5,6,7,7a-szesciowo- doro-4,7-metanoindanylo/]-N-etylotiokarbaminowego i l-fenylo-4-/a-hydroksy-j3,^-trójchloroetylo/amino-5-bro- mo-pirydazon-/6/.Ester etylowy kwasu N-l- lub 2-dwucyklo-[ 3,3,0 ]-oktylo-N-etylotiokarbaminowego i l-fenylo-4-/ a-hydroksy-j3, 0, (3-trójchloroetylo/ -amino-5-bromopirydazon-/6/. Ester S-etylowy kwasu N-dwucyklooktylo-/3,2,l/-N-propin-/- -2/ -ylo - /l/- tiokarbaminowego i l-fenylo-4-/ a-hydroksy-0, 0, j3-trójchloroetylo/ -amino-5-bromopirydazon-/6/.Cena 10 zl PL
Claims (1)
1. Zastrzezenie patentowe Srodek chwastobójczy, znamienny tym, ze jako substancje czynna zawiera mieszanine tiokarbami- nianu o wzorze 1, w którym R{ oznacza nizszy rodnik alkilowy lub alkinylowy zawierajacy do 4 atomów wegla, R2 oznacza rodnik cykloheksylowy, rodnik dwu- lub trójcykloalifatyczny zawierajacy do 8 atomów wegla, R3 oznacza nizszy rodnik alkilowy zawierajacy do 4 atomów wegla i zwiazku o wzorze 2, w którym Y oznacza atom chloru lub bromu i X oznacza grupe o wzorze -NH-CHOH-CCl3 lub o wzorze NH-CO-COO-R, w którym R ozna¬ cza IH-rzedowy rodnik butylowy lub izopropylowy.89 163 R 2\ yN-C-S-R; 1 O Wzór 1 Wzór 2 Prac.;P0ffgraf. UP PRL naklad 120+18 i "* PL
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2218347A DE2218347A1 (de) | 1972-04-15 | 1972-04-15 | Herbizid, |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PL89163B1 true PL89163B1 (pl) | 1976-10-30 |
Family
ID=5842101
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PL1973161904A PL89163B1 (pl) | 1972-04-15 | 1973-04-13 |
Country Status (20)
| Country | Link |
|---|---|
| US (1) | US3870502A (pl) |
| JP (1) | JPS4914637A (pl) |
| AR (1) | AR195220A1 (pl) |
| AT (2) | AT324037B (pl) |
| AU (1) | AU473687B2 (pl) |
| BE (1) | BE798137A (pl) |
| BG (3) | BG20272A3 (pl) |
| CH (1) | CH567355A5 (pl) |
| DD (1) | DD103544A5 (pl) |
| DE (1) | DE2218347A1 (pl) |
| ES (1) | ES413698A1 (pl) |
| FR (1) | FR2180803A1 (pl) |
| GB (1) | GB1419882A (pl) |
| HU (1) | HU166674B (pl) |
| IL (1) | IL41930A0 (pl) |
| IT (1) | IT980219B (pl) |
| NL (1) | NL7304486A (pl) |
| PL (1) | PL89163B1 (pl) |
| SU (1) | SU471694A3 (pl) |
| ZA (1) | ZA732556B (pl) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GR75597B (pl) * | 1980-04-28 | 1984-08-01 | Stauffer Chemical Co | |
| US4545810A (en) * | 1980-08-07 | 1985-10-08 | Sds Biotech Corporation | Herbicidal and plant growth regulant diphenylpyridazinones |
| CN105472984B (zh) * | 2012-11-30 | 2017-07-18 | 罗门哈斯公司 | 用于干膜保护的环草定与ipbc的协同性组合 |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3546343A (en) * | 1966-01-18 | 1970-12-08 | Union Carbide Corp | 4-(methylcarbamoyloxy) carbanilates as insecticides and nematocides |
| DE1921464A1 (de) * | 1969-04-26 | 1970-12-17 | Basf Ag | Herbizid |
| PH9237A (en) * | 1969-07-01 | 1975-07-30 | H Hagimoto | Herbicidal composition comprising oxa-or thiadiazole compounds |
-
1972
- 1972-04-15 DE DE2218347A patent/DE2218347A1/de active Pending
-
1973
- 1973-03-09 BG BG022942A patent/BG20272A3/xx unknown
- 1973-03-09 BG BG024863A patent/BG22782A3/xx unknown
- 1973-03-09 BG BG024864A patent/BG20997A3/xx unknown
- 1973-03-23 JP JP48032763A patent/JPS4914637A/ja active Pending
- 1973-03-28 AR AR247279A patent/AR195220A1/es active
- 1973-03-30 NL NL7304486A patent/NL7304486A/xx not_active Application Discontinuation
- 1973-04-02 IL IL41930A patent/IL41930A0/xx unknown
- 1973-04-04 AU AU54079/73A patent/AU473687B2/en not_active Expired
- 1973-04-04 US US348084A patent/US3870502A/en not_active Expired - Lifetime
- 1973-04-12 BE BE129944A patent/BE798137A/xx unknown
- 1973-04-12 SU SU1906704A patent/SU471694A3/ru active
- 1973-04-13 FR FR7313535A patent/FR2180803A1/fr not_active Withdrawn
- 1973-04-13 ZA ZA732556A patent/ZA732556B/xx unknown
- 1973-04-13 CH CH537273A patent/CH567355A5/xx not_active IP Right Cessation
- 1973-04-13 PL PL1973161904A patent/PL89163B1/pl unknown
- 1973-04-13 GB GB1781773A patent/GB1419882A/en not_active Expired
- 1973-04-13 HU HUBA2915A patent/HU166674B/hu unknown
- 1973-04-13 AT AT328473A patent/AT324037B/de not_active IP Right Cessation
- 1973-04-13 DD DD170174A patent/DD103544A5/xx unknown
- 1973-04-13 IT IT49454/73A patent/IT980219B/it active
- 1973-04-13 AT AT545874A patent/AT324040B/de not_active IP Right Cessation
- 1973-04-14 ES ES413698A patent/ES413698A1/es not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| FR2180803A1 (pl) | 1973-11-30 |
| AT324037B (de) | 1975-08-11 |
| CH567355A5 (pl) | 1975-10-15 |
| ZA732556B (en) | 1974-04-24 |
| AT324040B (de) | 1975-08-11 |
| SU471694A3 (ru) | 1975-05-25 |
| BG22782A3 (bg) | 1977-04-20 |
| ES413698A1 (es) | 1976-06-16 |
| NL7304486A (pl) | 1973-10-17 |
| US3870502A (en) | 1975-03-11 |
| AU473687B2 (en) | 1976-07-01 |
| AU5407973A (en) | 1974-10-10 |
| IL41930A0 (en) | 1973-06-29 |
| BE798137A (fr) | 1973-10-12 |
| BG20997A3 (bg) | 1976-01-20 |
| JPS4914637A (pl) | 1974-02-08 |
| GB1419882A (en) | 1975-12-31 |
| HU166674B (pl) | 1975-05-28 |
| BG20272A3 (bg) | 1975-11-05 |
| DE2218347A1 (de) | 1973-10-31 |
| DD103544A5 (pl) | 1974-02-05 |
| IT980219B (it) | 1974-09-30 |
| AR195220A1 (es) | 1973-09-19 |
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