CS208457B2 - Insicticide and acaricide means and method of making the active substances - Google Patents
Insicticide and acaricide means and method of making the active substances Download PDFInfo
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- CS208457B2 CS208457B2 CS796379A CS637979A CS208457B2 CS 208457 B2 CS208457 B2 CS 208457B2 CS 796379 A CS796379 A CS 796379A CS 637979 A CS637979 A CS 637979A CS 208457 B2 CS208457 B2 CS 208457B2
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- 239000013543 active substance Substances 0.000 title description 16
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- DWDXUUXYFBTWAP-UHFFFAOYSA-N ethyl 3-[2-bromo-2-(4-chlorophenyl)ethenyl]-2,2-dimethylcyclopropane-1-carboxylate Chemical compound CC1(C)C(C(=O)OCC)C1C=C(Br)C1=CC=C(Cl)C=C1 DWDXUUXYFBTWAP-UHFFFAOYSA-N 0.000 description 1
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- DNZPFPGYVWVLCE-UHFFFAOYSA-N hydroxy(phenyl)methanesulfonic acid Chemical class OS(=O)(=O)C(O)C1=CC=CC=C1 DNZPFPGYVWVLCE-UHFFFAOYSA-N 0.000 description 1
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- 229910052742 iron Inorganic materials 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
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- 239000004816 latex Substances 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- 229920005610 lignin Polymers 0.000 description 1
- 239000006028 limestone Substances 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
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- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
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- JCXJVPUVTGWSNB-UHFFFAOYSA-N nitrogen dioxide Inorganic materials O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 description 1
- 230000003071 parasitic effect Effects 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
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- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
- DLYUQMMRRRQYAE-UHFFFAOYSA-N phosphorus pentoxide Inorganic materials O1P(O2)(=O)OP3(=O)OP1(=O)OP2(=O)O3 DLYUQMMRRRQYAE-UHFFFAOYSA-N 0.000 description 1
- 239000001007 phthalocyanine dye Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- NNFCIKHAZHQZJG-UHFFFAOYSA-N potassium cyanide Chemical compound [K+].N#[C-] NNFCIKHAZHQZJG-UHFFFAOYSA-N 0.000 description 1
- RPDAUEIUDPHABB-UHFFFAOYSA-N potassium ethoxide Chemical compound [K+].CC[O-] RPDAUEIUDPHABB-UHFFFAOYSA-N 0.000 description 1
- 239000001294 propane Substances 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
- 229960000856 protein c Drugs 0.000 description 1
- 235000021251 pulses Nutrition 0.000 description 1
- 239000008262 pumice Substances 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000007127 saponification reaction Methods 0.000 description 1
- 208000005687 scabies Diseases 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L sodium carbonate Substances [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- SMDQFHZIWNYSMR-UHFFFAOYSA-N sulfanylidenemagnesium Chemical compound S=[Mg] SMDQFHZIWNYSMR-UHFFFAOYSA-N 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 1
- JLKIGFTWXXRPMT-UHFFFAOYSA-N sulphamethoxazole Chemical compound O1C(C)=CC(NS(=O)(=O)C=2C=CC(N)=CC=2)=N1 JLKIGFTWXXRPMT-UHFFFAOYSA-N 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- JRMUNVKIHCOMHV-UHFFFAOYSA-M tetrabutylammonium bromide Chemical compound [Br-].CCCC[N+](CCCC)(CCCC)CCCC JRMUNVKIHCOMHV-UHFFFAOYSA-M 0.000 description 1
- CZDYPVPMEAXLPK-UHFFFAOYSA-N tetramethylsilane Chemical compound C[Si](C)(C)C CZDYPVPMEAXLPK-UHFFFAOYSA-N 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 239000011573 trace mineral Substances 0.000 description 1
- 235000013619 trace mineral Nutrition 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 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
- A01N53/00—Biocides, pest repellants or attractants, or plant growth regulators containing cyclopropane carboxylic acids or derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C61/00—Compounds having carboxyl groups bound to carbon atoms of rings other than six-membered aromatic rings
- C07C61/16—Unsaturated compounds
- C07C61/40—Unsaturated compounds containing halogen
-
- 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
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/38—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
- C07F9/40—Esters thereof
- C07F9/4003—Esters thereof the acid moiety containing a substituent or a structure which is considered as characteristic
- C07F9/4056—Esters of arylalkanephosphonic acids
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Catalysts (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19782842542 DE2842542A1 (de) | 1978-09-29 | 1978-09-29 | Substituierte bromostyryl-cyclopropancarbonsaeurephenoxybenzylester, verfahren zu ihrer herstellunnd ihre verwendung als insektizide und akarizide |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CS208457B2 true CS208457B2 (en) | 1981-09-15 |
Family
ID=6050909
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CS796379A CS208457B2 (en) | 1978-09-29 | 1979-09-21 | Insicticide and acaricide means and method of making the active substances |
Country Status (24)
| Country | Link |
|---|---|
| US (1) | US4279920A (ko) |
| EP (1) | EP0009708B1 (ko) |
| JP (1) | JPS5549342A (ko) |
| AU (1) | AU525915B2 (ko) |
| BG (1) | BG30622A3 (ko) |
| BR (1) | BR7906170A (ko) |
| CA (1) | CA1136637A (ko) |
| CS (1) | CS208457B2 (ko) |
| DD (1) | DD147906A5 (ko) |
| DE (2) | DE2842542A1 (ko) |
| DK (1) | DK409579A (ko) |
| EG (1) | EG13806A (ko) |
| ES (1) | ES484576A1 (ko) |
| HU (2) | HU188495B (ko) |
| IL (1) | IL58331A (ko) |
| NZ (1) | NZ191679A (ko) |
| OA (1) | OA06349A (ko) |
| PH (1) | PH15309A (ko) |
| PL (1) | PL120441B1 (ko) |
| PT (1) | PT70223A (ko) |
| RO (1) | RO78867B (ko) |
| SU (1) | SU893121A3 (ko) |
| TR (1) | TR20537A (ko) |
| ZA (1) | ZA795165B (ko) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4376785A (en) * | 1980-06-19 | 1983-03-15 | Sumitomo Chemical Company, Limited | Cyclopropanecarboxylates and a low fish toxic insecticide and/or acaricide containing them |
| US4377532A (en) * | 1981-02-26 | 1983-03-22 | Ciba-Geigy Corporation | 3-Phenoxybenzyl compounds |
| DE3900275A1 (de) * | 1989-01-07 | 1990-07-12 | Basf Ag | Substituierte cyclopropancarbonsaeurepropargylester, verfahren zu ihrer herstellung und ihre verwendung zur bekaempfung von schaedlingen |
| US8124036B1 (en) | 2005-10-27 | 2012-02-28 | ADA-ES, Inc. | Additives for mercury oxidation in coal-fired power plants |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4024163A (en) * | 1972-05-25 | 1977-05-17 | National Research Development Corporation | Insecticides |
| JPS5813522B2 (ja) * | 1974-10-24 | 1983-03-14 | 住友化学工業株式会社 | 新しいシクロプロパンカルボン酸エステルを含有する殺虫、殺ダニ剤 |
| CH602005A5 (en) * | 1976-02-17 | 1978-07-14 | Ciba Geigy Ag | (3)-Phenoxy-benzyl styryl-cyclopropane carboxylates |
| NL7701321A (nl) * | 1976-02-17 | 1977-08-19 | Ciba Geigy | Werkwijze voor de bereiding van een ester. |
| ZA775160B (en) * | 1976-08-27 | 1978-07-26 | Fmc Corp | Insecticidal styryl- and substituted-styrylcyclopropanecarboxylates |
| CA1260486A (en) * | 1976-08-27 | 1989-09-26 | John F. Engel | Insecticidal styryl- and substituted- styrylcyclopropanecarboxylates |
| DE2730515A1 (de) * | 1977-07-06 | 1979-01-18 | Bayer Ag | Substituierte phenoxybenzyloxycarbonylderivate, verfahren zu ihrer herstellung und ihre verwendung als insektizide und akarizide |
| DE2739854A1 (de) * | 1977-09-03 | 1979-03-15 | Bayer Ag | Fluorsubstituierte phenoxybenzyloxycarbonylderivate, verfahren zu ihrer herstellung und ihre verwendung als insektizide und akarizide |
-
1978
- 1978-09-29 DE DE19782842542 patent/DE2842542A1/de not_active Ceased
-
1979
- 1979-09-10 US US06/074,045 patent/US4279920A/en not_active Expired - Lifetime
- 1979-09-17 DE DE7979103487T patent/DE2967304D1/de not_active Expired
- 1979-09-17 EP EP79103487A patent/EP0009708B1/de not_active Expired
- 1979-09-21 CS CS796379A patent/CS208457B2/cs unknown
- 1979-09-24 SU SU792817352A patent/SU893121A3/ru active
- 1979-09-25 TR TR20537A patent/TR20537A/xx unknown
- 1979-09-25 PT PT70223A patent/PT70223A/pt unknown
- 1979-09-25 BG BG044932A patent/BG30622A3/xx unknown
- 1979-09-26 PH PH23070A patent/PH15309A/en unknown
- 1979-09-26 BR BR7906170A patent/BR7906170A/pt unknown
- 1979-09-26 NZ NZ191679A patent/NZ191679A/xx unknown
- 1979-09-26 IL IL58331A patent/IL58331A/xx unknown
- 1979-09-27 PL PL1979218565A patent/PL120441B1/pl unknown
- 1979-09-27 AU AU51260/79A patent/AU525915B2/en not_active Ceased
- 1979-09-27 DD DD79215857A patent/DD147906A5/de unknown
- 1979-09-27 CA CA000336501A patent/CA1136637A/en not_active Expired
- 1979-09-28 HU HU833415A patent/HU188495B/hu not_active IP Right Cessation
- 1979-09-28 DK DK409579A patent/DK409579A/da not_active Application Discontinuation
- 1979-09-28 OA OA56908A patent/OA06349A/xx unknown
- 1979-09-28 HU HU79BA3857A patent/HU184682B/hu unknown
- 1979-09-28 ZA ZA00795165A patent/ZA795165B/xx unknown
- 1979-09-28 JP JP12427479A patent/JPS5549342A/ja active Granted
- 1979-09-28 ES ES484576A patent/ES484576A1/es not_active Expired
- 1979-09-29 RO RO98814A patent/RO78867B/ro unknown
- 1979-09-29 EG EG574/79A patent/EG13806A/xx active
Also Published As
| Publication number | Publication date |
|---|---|
| TR20537A (tr) | 1981-10-21 |
| CA1136637A (en) | 1982-11-30 |
| HU188495B (en) | 1986-04-28 |
| RO78867B (ro) | 1983-06-30 |
| US4279920A (en) | 1981-07-21 |
| EP0009708B1 (de) | 1984-11-21 |
| EP0009708A1 (de) | 1980-04-16 |
| NZ191679A (en) | 1981-05-15 |
| JPS636057B2 (ko) | 1988-02-08 |
| ES484576A1 (es) | 1980-06-16 |
| PT70223A (en) | 1979-10-01 |
| JPS5549342A (en) | 1980-04-09 |
| SU893121A3 (ru) | 1981-12-23 |
| OA06349A (fr) | 1981-06-30 |
| EG13806A (en) | 1982-06-30 |
| PL218565A1 (ko) | 1980-07-01 |
| AU5126079A (en) | 1980-04-03 |
| DE2967304D1 (en) | 1985-01-03 |
| DE2842542A1 (de) | 1980-04-17 |
| BR7906170A (pt) | 1980-05-27 |
| DK409579A (da) | 1980-03-30 |
| RO78867A (ro) | 1982-07-06 |
| PH15309A (en) | 1982-11-18 |
| PL120441B1 (en) | 1982-02-27 |
| IL58331A (en) | 1985-06-30 |
| AU525915B2 (en) | 1982-12-09 |
| BG30622A3 (en) | 1981-07-15 |
| DD147906A5 (de) | 1981-04-29 |
| HU184682B (en) | 1984-09-28 |
| IL58331A0 (en) | 1979-12-30 |
| ZA795165B (en) | 1980-10-29 |
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