SU791197A3 - Инсектоакарицидное средство - Google Patents
Инсектоакарицидное средство Download PDFInfo
- Publication number
- SU791197A3 SU791197A3 SU762378585A SU2378585A SU791197A3 SU 791197 A3 SU791197 A3 SU 791197A3 SU 762378585 A SU762378585 A SU 762378585A SU 2378585 A SU2378585 A SU 2378585A SU 791197 A3 SU791197 A3 SU 791197A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- methyl
- octyl
- hydrogen
- cyclopropylmethyl
- cyclohexyl
- Prior art date
Links
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 12
- 150000001875 compounds Chemical class 0.000 claims abstract description 8
- 239000001257 hydrogen Substances 0.000 claims abstract description 8
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 8
- 230000000895 acaricidal effect Effects 0.000 claims abstract description 7
- 230000000749 insecticidal effect Effects 0.000 claims abstract description 4
- 125000004433 nitrogen atom Chemical group N* 0.000 claims abstract 3
- 229910052757 nitrogen Inorganic materials 0.000 claims abstract 2
- -1 n-octyl Chemical group 0.000 claims description 11
- 125000004186 cyclopropylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C1([H])[H] 0.000 claims description 6
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 6
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 5
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 5
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 3
- 230000000694 effects Effects 0.000 claims description 3
- 239000002917 insecticide Substances 0.000 claims description 3
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 3
- 125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 claims description 3
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical group [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 2
- PNKUSGQVOMIXLU-UHFFFAOYSA-N Formamidine Chemical class NC=N PNKUSGQVOMIXLU-UHFFFAOYSA-N 0.000 claims description 2
- 150000001409 amidines Chemical class 0.000 claims description 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 2
- 229910052794 bromium Inorganic materials 0.000 claims description 2
- 239000003795 chemical substances by application Substances 0.000 claims description 2
- 239000000460 chlorine Chemical group 0.000 claims description 2
- 229910052801 chlorine Inorganic materials 0.000 claims description 2
- 239000000575 pesticide Substances 0.000 claims description 2
- 150000002431 hydrogen Chemical class 0.000 claims 3
- 239000000654 additive Substances 0.000 claims 1
- 125000001309 chloro group Chemical group Cl* 0.000 claims 1
- 239000003085 diluting agent Substances 0.000 claims 1
- 239000000945 filler Substances 0.000 claims 1
- 239000002574 poison Substances 0.000 claims 1
- 231100000614 poison Toxicity 0.000 claims 1
- 125000000719 pyrrolidinyl group Chemical group 0.000 claims 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 abstract description 4
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 5
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 abstract 3
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 1
- 125000002373 5 membered heterocyclic group Chemical group 0.000 abstract 1
- 125000004070 6 membered heterocyclic group Chemical group 0.000 abstract 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 1
- 125000004122 cyclic group Chemical group 0.000 abstract 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- 239000001301 oxygen Substances 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 241000196324 Embryophyta Species 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 238000002474 experimental method Methods 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 241001454294 Tetranychus Species 0.000 description 2
- 239000013543 active substance Substances 0.000 description 2
- PWMWNFMRSKOCEY-UHFFFAOYSA-N 1-Phenyl-1,2-ethanediol Chemical compound OCC(O)C1=CC=CC=C1 PWMWNFMRSKOCEY-UHFFFAOYSA-N 0.000 description 1
- 241000426497 Chilo suppressalis Species 0.000 description 1
- 229940126062 Compound A Drugs 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
- 241001465754 Metazoa Species 0.000 description 1
- IFIHMDDBCWWPRF-UHFFFAOYSA-N N'-(4-chloro-2-methylphenyl)ethanimidamide Chemical compound CC(=NC1=C(C=C(C=C1)Cl)C)N IFIHMDDBCWWPRF-UHFFFAOYSA-N 0.000 description 1
- 240000007594 Oryza sativa Species 0.000 description 1
- 235000007164 Oryza sativa Nutrition 0.000 description 1
- 244000046052 Phaseolus vulgaris Species 0.000 description 1
- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 1
- 241000220221 Rosales Species 0.000 description 1
- 241000607479 Yersinia pestis Species 0.000 description 1
- 239000000642 acaricide Substances 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 230000004071 biological effect Effects 0.000 description 1
- 229940088623 biologically active substance Drugs 0.000 description 1
- CDKRVFYWESMRSP-UHFFFAOYSA-N chloro thiohypochlorite;1,1,3-trimethylurea Chemical compound ClSCl.CNC(=O)N(C)C CDKRVFYWESMRSP-UHFFFAOYSA-N 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- FHIVAFMUCKRCQO-UHFFFAOYSA-N diazinon Chemical compound CCOP(=S)(OCC)OC1=CC(C)=NC(C(C)C)=N1 FHIVAFMUCKRCQO-UHFFFAOYSA-N 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- UFEJKYYYVXYMMS-UHFFFAOYSA-N methylcarbamic acid Chemical compound CNC(O)=O UFEJKYYYVXYMMS-UHFFFAOYSA-N 0.000 description 1
- 239000004476 plant protection product Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- ILWRPSCZWQJDMK-UHFFFAOYSA-N triethylazanium;chloride Chemical compound Cl.CCN(CC)CC ILWRPSCZWQJDMK-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/16—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms
- C07D295/20—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms by radicals derived from carbonic acid, or sulfur or nitrogen analogues thereof
- C07D295/215—Radicals derived from nitrogen analogues of carbonic acid
-
- 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
- A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
- A01N47/34—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the groups, e.g. biuret; Thio analogues thereof; Urea-aldehyde condensation products
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C381/00—Compounds containing carbon and sulfur and having functional groups not covered by groups C07C301/00 - C07C337/00
- C07C381/06—Compounds containing sulfur atoms only bound to two nitrogen atoms
- C07C381/08—Compounds containing sulfur atoms only bound to two nitrogen atoms having at least one of the nitrogen atoms acylated
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/12—Systems containing only non-condensed rings with a six-membered ring
- C07C2601/14—The ring being saturated
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Dentistry (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Agronomy & Crop Science (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH967475A CH612421A5 (en) | 1975-07-24 | 1975-07-24 | Pesticide comprising a (N-methyl- N'-phenylformamidino-mercapto)urea as active ingredient |
| CH190976 | 1976-02-17 | ||
| CH702076 | 1976-06-03 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU791197A3 true SU791197A3 (ru) | 1980-12-23 |
Family
ID=27173337
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU762378585A SU791197A3 (ru) | 1975-07-24 | 1976-07-08 | Инсектоакарицидное средство |
Country Status (15)
| Country | Link |
|---|---|
| US (1) | US4098902A (enExample) |
| JP (1) | JPS5214729A (enExample) |
| AT (1) | AT350321B (enExample) |
| AU (1) | AU505161B2 (enExample) |
| BR (1) | BR7604811A (enExample) |
| CA (1) | CA1060035A (enExample) |
| DE (1) | DE2632692A1 (enExample) |
| EG (1) | EG12061A (enExample) |
| FR (1) | FR2318867A1 (enExample) |
| GB (1) | GB1538764A (enExample) |
| IL (1) | IL50105A (enExample) |
| MX (1) | MX3484E (enExample) |
| NL (1) | NL7608219A (enExample) |
| SU (1) | SU791197A3 (enExample) |
| TR (1) | TR19146A (enExample) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2737606A1 (de) * | 1977-08-20 | 1979-03-01 | Bayer Ag | Aryl-n-alkyl-carbamate, verfahren zu ihrer herstellung und ihre verwendung als insektizide |
| US4369189A (en) * | 1980-12-10 | 1983-01-18 | Union Carbide Corporation | Novel unsymmetrical formamidine-sulfenylated carbamate compounds |
| AU572825B2 (en) * | 1983-03-03 | 1988-05-19 | Fmc Corporation (Uk) Limited | Inhibition of corrosion and scale formation of metal surfaces |
| CA1339745C (en) * | 1984-04-10 | 1998-03-17 | Martin Anderson | Pesticidal benzoylurea compounds |
| JPS62290780A (ja) * | 1986-06-09 | 1987-12-17 | Sunstar Giken Kk | 一液型クロロプレン系接着剤 |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3853966A (en) * | 1970-11-09 | 1974-12-10 | G Kohn | N-chlorothio ureas |
| US3857883A (en) * | 1972-05-08 | 1974-12-31 | Chevron Res | N-chlorothio urea production |
| US3947591A (en) * | 1975-05-07 | 1976-03-30 | The Upjohn Company | Pesticidal N,N"-thio and dithio bis(substituted phenyl formamidines) |
-
1976
- 1976-07-08 SU SU762378585A patent/SU791197A3/ru active
- 1976-07-20 US US05/707,149 patent/US4098902A/en not_active Expired - Lifetime
- 1976-07-20 FR FR7622120A patent/FR2318867A1/fr active Granted
- 1976-07-21 DE DE19762632692 patent/DE2632692A1/de not_active Withdrawn
- 1976-07-22 TR TR19146A patent/TR19146A/xx unknown
- 1976-07-22 AU AU16127/76A patent/AU505161B2/en not_active Expired
- 1976-07-22 IL IL7650105A patent/IL50105A/xx unknown
- 1976-07-22 CA CA257,577A patent/CA1060035A/en not_active Expired
- 1976-07-23 BR BR7604811A patent/BR7604811A/pt unknown
- 1976-07-23 GB GB30873/76A patent/GB1538764A/en not_active Expired
- 1976-07-23 NL NL7608219A patent/NL7608219A/xx not_active Application Discontinuation
- 1976-07-23 MX MX001795U patent/MX3484E/es unknown
- 1976-07-23 AT AT545076A patent/AT350321B/de not_active IP Right Cessation
- 1976-07-24 JP JP51088614A patent/JPS5214729A/ja active Pending
- 1976-07-25 EG EG449/76A patent/EG12061A/xx active
Also Published As
| Publication number | Publication date |
|---|---|
| DE2632692A1 (de) | 1977-02-10 |
| AT350321B (de) | 1979-05-25 |
| JPS5214729A (en) | 1977-02-03 |
| AU505161B2 (en) | 1979-11-08 |
| CA1060035A (en) | 1979-08-07 |
| FR2318867A1 (fr) | 1977-02-18 |
| ATA545076A (de) | 1978-10-15 |
| EG12061A (en) | 1978-06-30 |
| BR7604811A (pt) | 1977-08-02 |
| AU1612776A (en) | 1978-01-26 |
| IL50105A (en) | 1979-12-30 |
| IL50105A0 (en) | 1976-09-30 |
| NL7608219A (nl) | 1977-01-26 |
| US4098902A (en) | 1978-07-04 |
| GB1538764A (en) | 1979-01-24 |
| FR2318867B1 (enExample) | 1979-06-08 |
| TR19146A (tr) | 1978-07-01 |
| MX3484E (es) | 1980-12-16 |
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