SU888801A3 - Инсектцидна композици - Google Patents
Инсектцидна композици Download PDFInfo
- Publication number
- SU888801A3 SU888801A3 SU731920459A SU1920459A SU888801A3 SU 888801 A3 SU888801 A3 SU 888801A3 SU 731920459 A SU731920459 A SU 731920459A SU 1920459 A SU1920459 A SU 1920459A SU 888801 A3 SU888801 A3 SU 888801A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- alkyl
- hydrogen
- aryl
- aralkyl
- alkenyl
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims description 11
- 239000002917 insecticide Substances 0.000 title abstract description 4
- 150000001875 compounds Chemical class 0.000 claims abstract description 24
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 15
- 239000001257 hydrogen Substances 0.000 claims abstract description 15
- -1 lactam acetal Chemical class 0.000 claims abstract description 8
- 125000000217 alkyl group Chemical group 0.000 claims abstract 16
- SKKTZJVNTSSCLS-WAYWQWQTSA-N (2z)-2-(nitromethylidene)piperidine Chemical compound [O-][N+](=O)\C=C1\CCCCN1 SKKTZJVNTSSCLS-WAYWQWQTSA-N 0.000 claims abstract 2
- 230000000749 insecticidal effect Effects 0.000 claims description 10
- 239000000460 chlorine Substances 0.000 claims description 7
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 6
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 6
- 241000255925 Diptera Species 0.000 claims description 6
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 6
- 229910052794 bromium Inorganic materials 0.000 claims description 6
- 229910052801 chlorine Inorganic materials 0.000 claims description 6
- 239000013543 active substance Substances 0.000 claims description 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 4
- 150000002431 hydrogen Chemical group 0.000 claims description 4
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims description 3
- COVZYZSDYWQREU-UHFFFAOYSA-N Busulfan Chemical compound CS(=O)(=O)OCCCCOS(C)(=O)=O COVZYZSDYWQREU-UHFFFAOYSA-N 0.000 claims description 3
- 239000000654 additive Substances 0.000 claims description 3
- 230000000996 additive effect Effects 0.000 claims description 3
- CCIVGXIOQKPBKL-UHFFFAOYSA-M ethanesulfonate Chemical compound CCS([O-])(=O)=O CCIVGXIOQKPBKL-UHFFFAOYSA-M 0.000 claims description 3
- 229910052731 fluorine Inorganic materials 0.000 claims description 3
- 239000011737 fluorine Substances 0.000 claims description 3
- 125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 claims description 3
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 3
- 125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 claims description 2
- 239000000575 pesticide Substances 0.000 claims description 2
- 239000002904 solvent Substances 0.000 claims description 2
- 231100000419 toxicity Toxicity 0.000 claims description 2
- 230000001988 toxicity Effects 0.000 claims description 2
- 241000256244 Heliothis virescens Species 0.000 claims 1
- 239000004480 active ingredient Substances 0.000 claims 1
- 229910052740 iodine Inorganic materials 0.000 claims 1
- 239000011630 iodine Substances 0.000 claims 1
- 239000007787 solid Substances 0.000 claims 1
- 239000004094 surface-active agent Substances 0.000 claims 1
- 231100000167 toxic agent Toxicity 0.000 claims 1
- XUWHAWMETYGRKB-UHFFFAOYSA-N piperidin-2-one Chemical compound O=C1CCCCN1 XUWHAWMETYGRKB-UHFFFAOYSA-N 0.000 abstract description 7
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract description 5
- 238000002360 preparation method Methods 0.000 abstract description 3
- SKKTZJVNTSSCLS-UHFFFAOYSA-N 2-(nitromethylidene)piperidine Chemical class [O-][N+](=O)C=C1CCCCN1 SKKTZJVNTSSCLS-UHFFFAOYSA-N 0.000 abstract description 2
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 abstract description 2
- 150000004703 alkoxides Chemical class 0.000 abstract description 2
- LYGJENNIWJXYER-UHFFFAOYSA-N nitromethane Chemical compound C[N+]([O-])=O LYGJENNIWJXYER-UHFFFAOYSA-N 0.000 abstract description 2
- 125000003342 alkenyl group Chemical group 0.000 abstract 3
- 125000003118 aryl group Chemical group 0.000 abstract 3
- 229910052736 halogen Inorganic materials 0.000 abstract 3
- 125000000304 alkynyl group Chemical group 0.000 abstract 2
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 2
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 2
- 150000002367 halogens Chemical group 0.000 abstract 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 125000004183 alkoxy alkyl group Chemical group 0.000 abstract 1
- 229910052799 carbon Inorganic materials 0.000 abstract 1
- 125000004966 cyanoalkyl group Chemical group 0.000 abstract 1
- 125000000717 hydrazino group Chemical group [H]N([*])N([H])[H] 0.000 abstract 1
- LYGJENNIWJXYER-BJUDXGSMSA-N nitromethane Chemical class [11CH3][N+]([O-])=O LYGJENNIWJXYER-BJUDXGSMSA-N 0.000 abstract 1
- 150000003053 piperidines Chemical class 0.000 abstract 1
- 125000001424 substituent group Chemical group 0.000 abstract 1
- 229910021653 sulphate ion Inorganic materials 0.000 abstract 1
- 238000012360 testing method Methods 0.000 description 13
- 241000238631 Hexapoda Species 0.000 description 6
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- 239000000725 suspension Substances 0.000 description 4
- LKMGDZMCCPSUFI-PLNGDYQASA-N (2z)-2-(nitromethylidene)pyrrolidine Chemical compound [O-][N+](=O)\C=C1\CCCN1 LKMGDZMCCPSUFI-PLNGDYQASA-N 0.000 description 3
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 2
- SBPBAQFWLVIOKP-UHFFFAOYSA-N chlorpyrifos Chemical compound CCOP(=S)(OCC)OC1=NC(Cl)=C(Cl)C=C1Cl SBPBAQFWLVIOKP-UHFFFAOYSA-N 0.000 description 2
- 238000013101 initial test Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- IWZSHWBGHQBIML-ZGGLMWTQSA-N (3S,8S,10R,13S,14S,17S)-17-isoquinolin-7-yl-N,N,10,13-tetramethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-amine Chemical compound CN(C)[C@H]1CC[C@]2(C)C3CC[C@@]4(C)[C@@H](CC[C@@H]4c4ccc5ccncc5c4)[C@@H]3CC=C2C1 IWZSHWBGHQBIML-ZGGLMWTQSA-N 0.000 description 1
- 241000449794 Alabama argillacea Species 0.000 description 1
- 125000000174 L-prolyl group Chemical group [H]N1C([H])([H])C([H])([H])C([H])([H])[C@@]1([H])C(*)=O 0.000 description 1
- 241000257226 Muscidae Species 0.000 description 1
- 244000061176 Nicotiana tabacum Species 0.000 description 1
- 235000002637 Nicotiana tabacum Nutrition 0.000 description 1
- 240000007594 Oryza sativa Species 0.000 description 1
- 235000007164 Oryza sativa Nutrition 0.000 description 1
- 239000000443 aerosol Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 150000008050 dialkyl sulfates Chemical class 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 125000006216 methylsulfinyl group Chemical group [H]C([H])([H])S(*)=O 0.000 description 1
- 230000004899 motility Effects 0.000 description 1
- 239000004476 plant protection product Substances 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/68—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member
- C07D211/72—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, directly attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/68—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member
- C07D211/72—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D211/74—Oxygen atoms
- C07D211/76—Oxygen atoms attached in position 2 or 6
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Hydrogenated Pyridines (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US25030572A | 1972-05-04 | 1972-05-04 | |
| US25030672A | 1972-05-04 | 1972-05-04 | |
| US33115873A | 1973-02-09 | 1973-02-09 | |
| US00331155A US3853888A (en) | 1972-05-04 | 1973-02-09 | Piperidine insect control agents |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU888801A3 true SU888801A3 (ru) | 1981-12-07 |
Family
ID=27500350
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU731920459A SU888801A3 (ru) | 1972-05-04 | 1973-05-03 | Инсектцидна композици |
Country Status (16)
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6184234A (ja) * | 1984-10-03 | 1986-04-28 | 藤森工業株式会社 | 包装袋の製造方法 |
| CN1120839A (zh) * | 1993-04-08 | 1996-04-17 | 希巴-盖吉股份公司 | 新的2-硝基亚甲基/2-氰基亚氨基/2-硝基亚氨基-吡咯烷和哌啶，中间体，和其作为杀虫剂的用途 |
| US6838567B1 (en) | 1999-05-14 | 2005-01-04 | Kaneka Corporation | Process for producing optically active azetidine-2-carboxylic acids |
| CN1501917A (zh) * | 2000-08-30 | 2004-06-02 | 美国陶氏益农公司 | 杀虫剂用化合物、杀螨剂用化合物及其使用和制备方法 |
-
1973
- 1973-04-10 CA CA168,384A patent/CA978964A/en not_active Expired
- 1973-04-27 DE DE2321523A patent/DE2321523A1/de active Granted
- 1973-05-01 NL NL7306020A patent/NL7306020A/xx not_active Application Discontinuation
- 1973-05-02 DD DD170561A patent/DD105558A5/xx unknown
- 1973-05-02 CH CH623473A patent/CH583510A5/xx not_active IP Right Cessation
- 1973-05-02 PL PL1973162262A patent/PL89228B1/pl unknown
- 1973-05-02 AU AU55140/73A patent/AU472504B2/en not_active Expired
- 1973-05-02 HU HU73SE1675A patent/HU168688B/hu unknown
- 1973-05-02 IL IL42170A patent/IL42170A/xx unknown
- 1973-05-02 GB GB2081973A patent/GB1425763A/en not_active Expired
- 1973-05-02 FR FR7315715A patent/FR2196335B1/fr not_active Expired
- 1973-05-02 JP JP4859473A patent/JPS5626643B2/ja not_active Expired
- 1973-05-02 IT IT23620/73A patent/IT986985B/it active
- 1973-05-02 OA OA54893A patent/OA04404A/xx unknown
- 1973-05-03 SU SU731920459A patent/SU888801A3/ru active
- 1973-05-03 EG EG159/73A patent/EG10835A/xx active
Also Published As
| Publication number | Publication date |
|---|---|
| CA978964A (en) | 1975-12-02 |
| AU5514073A (en) | 1974-11-07 |
| NL7306020A (enrdf_load_stackoverflow) | 1973-11-06 |
| CH583510A5 (enrdf_load_stackoverflow) | 1977-01-14 |
| EG10835A (en) | 1976-07-31 |
| JPS4954532A (enrdf_load_stackoverflow) | 1974-05-27 |
| OA04404A (fr) | 1980-02-29 |
| IL42170A (en) | 1977-07-31 |
| JPS5626643B2 (enrdf_load_stackoverflow) | 1981-06-19 |
| HU168688B (en) | 1976-06-28 |
| DE2321523C2 (enrdf_load_stackoverflow) | 1987-09-17 |
| DD105558A5 (enrdf_load_stackoverflow) | 1974-05-05 |
| GB1425763A (en) | 1976-02-18 |
| FR2196335B1 (enrdf_load_stackoverflow) | 1977-02-11 |
| PL89228B1 (en) | 1976-11-30 |
| AU472504B2 (en) | 1976-05-27 |
| IL42170A0 (en) | 1973-07-30 |
| IT986985B (it) | 1975-01-30 |
| FR2196335A1 (enrdf_load_stackoverflow) | 1974-03-15 |
| DE2321523A1 (de) | 1973-11-15 |
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