GB1267998A - Insecticidal and acaricidal benzimidazole compositions - Google Patents
Insecticidal and acaricidal benzimidazole compositionsInfo
- Publication number
- GB1267998A GB1267998A GB22589/69A GB2258969A GB1267998A GB 1267998 A GB1267998 A GB 1267998A GB 22589/69 A GB22589/69 A GB 22589/69A GB 2258969 A GB2258969 A GB 2258969A GB 1267998 A GB1267998 A GB 1267998A
- Authority
- GB
- United Kingdom
- Prior art keywords
- hydrogen
- methyl
- fluorine
- trade mark
- chlorine
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 239000000203 mixture Substances 0.000 title abstract 3
- 230000000895 acaricidal effect Effects 0.000 title abstract 2
- 230000000749 insecticidal effect Effects 0.000 title abstract 2
- HYZJCKYKOHLVJF-UHFFFAOYSA-N 1H-benzimidazole Chemical compound C1=CC=C2NC=NC2=C1 HYZJCKYKOHLVJF-UHFFFAOYSA-N 0.000 title 1
- 239000001257 hydrogen Substances 0.000 abstract 5
- 229910052739 hydrogen Inorganic materials 0.000 abstract 5
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 5
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical group FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 abstract 4
- 229910052731 fluorine Inorganic materials 0.000 abstract 4
- 239000011737 fluorine Chemical group 0.000 abstract 4
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical group [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 abstract 3
- -1 aldrin Chemical compound 0.000 abstract 3
- 125000000217 alkyl group Chemical group 0.000 abstract 3
- 229910052801 chlorine Inorganic materials 0.000 abstract 3
- 239000000460 chlorine Chemical group 0.000 abstract 3
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 abstract 2
- 229910052784 alkaline earth metal Inorganic materials 0.000 abstract 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 abstract 2
- 229910052794 bromium Inorganic materials 0.000 abstract 2
- JLYXXMFPNIAWKQ-UHFFFAOYSA-N γ Benzene hexachloride Chemical compound ClC1C(Cl)C(Cl)C(Cl)C(Cl)C1Cl JLYXXMFPNIAWKQ-UHFFFAOYSA-N 0.000 abstract 2
- ZCVAOQKBXKSDMS-AQYZNVCMSA-N (+)-trans-allethrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OC1C(C)=C(CC=C)C(=O)C1 ZCVAOQKBXKSDMS-AQYZNVCMSA-N 0.000 abstract 1
- IAKOZHOLGAGEJT-UHFFFAOYSA-N 1,1,1-trichloro-2,2-bis(p-methoxyphenyl)-Ethane Chemical compound C1=CC(OC)=CC=C1C(C(Cl)(Cl)Cl)C1=CC=C(OC)C=C1 IAKOZHOLGAGEJT-UHFFFAOYSA-N 0.000 abstract 1
- FMTFEIJHMMQUJI-NJAFHUGGSA-N 102130-98-3 Natural products CC=CCC1=C(C)[C@H](CC1=O)OC(=O)[C@@H]1[C@@H](C=C(C)C)C1(C)C FMTFEIJHMMQUJI-NJAFHUGGSA-N 0.000 abstract 1
- ZVZQKNVMDKSGGF-UHFFFAOYSA-N 2-ethylsulfanylethoxy-dimethoxy-sulfanylidene-$l^{5}-phosphane Chemical compound CCSCCOP(=S)(OC)OC ZVZQKNVMDKSGGF-UHFFFAOYSA-N 0.000 abstract 1
- XLOPRKKSAJMMEW-SFYZADRCSA-N Chrysanthemic acid Natural products CC(C)=C[C@@H]1[C@@H](C(O)=O)C1(C)C XLOPRKKSAJMMEW-SFYZADRCSA-N 0.000 abstract 1
- SOVGAJCNOMANBK-UHFFFAOYSA-N ClCCS(O)(O)(=O)C(C)COC1=CC=C(C(C)(C)C)C=C1 Chemical compound ClCCS(O)(O)(=O)C(C)COC1=CC=C(C(C)(C)C)C=C1 SOVGAJCNOMANBK-UHFFFAOYSA-N 0.000 abstract 1
- YVGGHNCTFXOJCH-UHFFFAOYSA-N DDT Chemical compound C1=CC(Cl)=CC=C1C(C(Cl)(Cl)Cl)C1=CC=C(Cl)C=C1 YVGGHNCTFXOJCH-UHFFFAOYSA-N 0.000 abstract 1
- 239000005947 Dimethoate Substances 0.000 abstract 1
- JHJOOSLFWRRSGU-UHFFFAOYSA-N Fenchlorphos Chemical compound COP(=S)(OC)OC1=CC(Cl)=C(Cl)C=C1Cl JHJOOSLFWRRSGU-UHFFFAOYSA-N 0.000 abstract 1
- 101000834981 Homo sapiens Testis, prostate and placenta-expressed protein Proteins 0.000 abstract 1
- 239000005949 Malathion Substances 0.000 abstract 1
- YNEVBPNZHBAYOA-UHFFFAOYSA-N Mexacarbate Chemical compound CNC(=O)OC1=CC(C)=C(N(C)C)C(C)=C1 YNEVBPNZHBAYOA-UHFFFAOYSA-N 0.000 abstract 1
- 229910019142 PO4 Inorganic materials 0.000 abstract 1
- VQXSOUPNOZTNAI-UHFFFAOYSA-N Pyrethrin I Natural products CC(=CC1CC1C(=O)OC2CC(=O)C(=C2C)CC=C/C=C)C VQXSOUPNOZTNAI-UHFFFAOYSA-N 0.000 abstract 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical class OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 abstract 1
- IDCBOTIENDVCBQ-UHFFFAOYSA-N TEPP Chemical compound CCOP(=O)(OCC)OP(=O)(OCC)OCC IDCBOTIENDVCBQ-UHFFFAOYSA-N 0.000 abstract 1
- 102100026164 Testis, prostate and placenta-expressed protein Human genes 0.000 abstract 1
- CRPUJAZIXJMDBK-UHFFFAOYSA-N Toxaphene Natural products C1CC2C(=C)C(C)(C)C1C2 CRPUJAZIXJMDBK-UHFFFAOYSA-N 0.000 abstract 1
- AVUYXHYHTTVPRX-UHFFFAOYSA-N Tris(2-methyl-1-aziridinyl)phosphine oxide Chemical compound CC1CN1P(=O)(N1C(C1)C)N1C(C)C1 AVUYXHYHTTVPRX-UHFFFAOYSA-N 0.000 abstract 1
- 239000003513 alkali Substances 0.000 abstract 1
- 150000001342 alkaline earth metals Chemical class 0.000 abstract 1
- 125000003342 alkenyl group Chemical group 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 125000000304 alkynyl group Chemical group 0.000 abstract 1
- 229940024113 allethrin Drugs 0.000 abstract 1
- 150000001556 benzimidazoles Chemical class 0.000 abstract 1
- 150000004657 carbamic acid derivatives Chemical class 0.000 abstract 1
- CVXBEEMKQHEXEN-UHFFFAOYSA-N carbaryl Chemical compound C1=CC=C2C(OC(=O)NC)=CC=CC2=C1 CVXBEEMKQHEXEN-UHFFFAOYSA-N 0.000 abstract 1
- 229960005286 carbaryl Drugs 0.000 abstract 1
- BIWJNBZANLAXMG-YQELWRJZSA-N chloordaan Chemical compound ClC1=C(Cl)[C@@]2(Cl)C3CC(Cl)C(Cl)C3[C@]1(Cl)C2(Cl)Cl BIWJNBZANLAXMG-YQELWRJZSA-N 0.000 abstract 1
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 abstract 1
- XLOPRKKSAJMMEW-UHFFFAOYSA-N chrysanthemic acid Chemical compound CC(C)=CC1C(C(O)=O)C1(C)C XLOPRKKSAJMMEW-UHFFFAOYSA-N 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- FHIVAFMUCKRCQO-UHFFFAOYSA-N diazinon Chemical compound CCOP(=S)(OCC)OC1=CC(C)=NC(C(C)C)=N1 FHIVAFMUCKRCQO-UHFFFAOYSA-N 0.000 abstract 1
- DFBKLUNHFCTMDC-PICURKEMSA-N dieldrin Chemical compound C([C@H]1[C@H]2[C@@]3(Cl)C(Cl)=C([C@]([C@H]22)(Cl)C3(Cl)Cl)Cl)[C@H]2[C@@H]2[C@H]1O2 DFBKLUNHFCTMDC-PICURKEMSA-N 0.000 abstract 1
- 229950006824 dieldrin Drugs 0.000 abstract 1
- NGPMUTDCEIKKFM-UHFFFAOYSA-N dieldrin Natural products CC1=C(Cl)C2(Cl)C3C4CC(C5OC45)C3C1(Cl)C2(Cl)Cl NGPMUTDCEIKKFM-UHFFFAOYSA-N 0.000 abstract 1
- FAXIJTUDSBIMHY-UHFFFAOYSA-N diethoxy-(2-ethylsulfanylethoxy)-sulfanylidene-$l^{5}-phosphane;1-diethoxyphosphorylsulfanyl-2-ethylsulfanylethane Chemical compound CCOP(=O)(OCC)SCCSCC.CCOP(=S)(OCC)OCCSCC FAXIJTUDSBIMHY-UHFFFAOYSA-N 0.000 abstract 1
- JXSJBGJIGXNWCI-UHFFFAOYSA-N diethyl 2-[(dimethoxyphosphorothioyl)thio]succinate Chemical compound CCOC(=O)CC(SP(=S)(OC)OC)C(=O)OCC JXSJBGJIGXNWCI-UHFFFAOYSA-N 0.000 abstract 1
- MCWXGJITAZMZEV-UHFFFAOYSA-N dimethoate Chemical compound CNC(=O)CSP(=S)(OC)OC MCWXGJITAZMZEV-UHFFFAOYSA-N 0.000 abstract 1
- DFBKLUNHFCTMDC-GKRDHZSOSA-N endrin Chemical compound C([C@@H]1[C@H]2[C@@]3(Cl)C(Cl)=C([C@]([C@H]22)(Cl)C3(Cl)Cl)Cl)[C@@H]2[C@H]2[C@@H]1O2 DFBKLUNHFCTMDC-GKRDHZSOSA-N 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- RIZMRRKBZQXFOY-UHFFFAOYSA-N ethion Chemical compound CCOP(=S)(OCC)SCSP(=S)(OCC)OCC RIZMRRKBZQXFOY-UHFFFAOYSA-N 0.000 abstract 1
- JLYXXMFPNIAWKQ-GNIYUCBRSA-N gamma-hexachlorocyclohexane Chemical compound Cl[C@H]1[C@H](Cl)[C@@H](Cl)[C@@H](Cl)[C@H](Cl)[C@H]1Cl JLYXXMFPNIAWKQ-GNIYUCBRSA-N 0.000 abstract 1
- 125000000262 haloalkenyl group Chemical group 0.000 abstract 1
- 125000001188 haloalkyl group Chemical group 0.000 abstract 1
- 125000001475 halogen functional group Chemical group 0.000 abstract 1
- FRCCEHPWNOQAEU-UHFFFAOYSA-N heptachlor Chemical compound ClC1=C(Cl)C2(Cl)C3C=CC(Cl)C3C1(Cl)C2(Cl)Cl FRCCEHPWNOQAEU-UHFFFAOYSA-N 0.000 abstract 1
- 239000002917 insecticide Substances 0.000 abstract 1
- 229960002809 lindane Drugs 0.000 abstract 1
- 229960000453 malathion Drugs 0.000 abstract 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
- LCCNCVORNKJIRZ-UHFFFAOYSA-N parathion Chemical compound CCOP(=S)(OCC)OC1=CC=C([N+]([O-])=O)C=C1 LCCNCVORNKJIRZ-UHFFFAOYSA-N 0.000 abstract 1
- RLBIQVVOMOPOHC-UHFFFAOYSA-N parathion-methyl Chemical compound COP(=S)(OC)OC1=CC=C([N+]([O-])=O)C=C1 RLBIQVVOMOPOHC-UHFFFAOYSA-N 0.000 abstract 1
- 125000006340 pentafluoro ethyl group Chemical group FC(F)(F)C(F)(F)* 0.000 abstract 1
- RGSFGYAAUTVSQA-UHFFFAOYSA-N pentamethylene Natural products C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 abstract 1
- 125000004817 pentamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 abstract 1
- 239000000575 pesticide Substances 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- 235000021317 phosphate Nutrition 0.000 abstract 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 abstract 1
- HYJYGLGUBUDSLJ-UHFFFAOYSA-N pyrethrin Natural products CCC(=O)OC1CC(=C)C2CC3OC3(C)C2C2OC(=O)C(=C)C12 HYJYGLGUBUDSLJ-UHFFFAOYSA-N 0.000 abstract 1
- VJFUPGQZSXIULQ-XIGJTORUSA-N pyrethrin II Chemical compound CC1(C)[C@H](/C=C(\C)C(=O)OC)[C@H]1C(=O)O[C@@H]1C(C)=C(C\C=C/C=C)C(=O)C1 VJFUPGQZSXIULQ-XIGJTORUSA-N 0.000 abstract 1
- 229940080817 rotenone Drugs 0.000 abstract 1
- JUVIOZPCNVVQFO-UHFFFAOYSA-N rotenone Natural products O1C2=C3CC(C(C)=C)OC3=CC=C2C(=O)C2C1COC1=C2C=C(OC)C(OC)=C1 JUVIOZPCNVVQFO-UHFFFAOYSA-N 0.000 abstract 1
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 abstract 1
- OEJNXTAZZBRGDN-UHFFFAOYSA-N toxaphene Chemical compound ClC1C(Cl)C2(Cl)C(CCl)(CCl)C(=C)C1(Cl)C2(Cl)Cl OEJNXTAZZBRGDN-UHFFFAOYSA-N 0.000 abstract 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
- C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
- C07D235/22—Benzimidazoles; Hydrogenated benzimidazoles with hetero atoms directly attached to ring nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
- C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
- C07D235/06—Benzimidazoles; Hydrogenated benzimidazoles with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached in position 2
- C07D235/10—Radicals substituted by halogen atoms or nitro radicals
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
1,267,998. Pesticides containing benzimidazoles. ELI LILLY & CO. 2 May, 1969 [3 May, 1968], No. 22589/69. Heading A5E. Insecticidal and acaricidal compositions comprise, in combination with a carrier, a compound of formula wherein R is hydrogen, an alkali or alkaline earth metal, or a group of formula R" O CO- or R"' R"" NCS-, wherein R' is hydrogen, fluorine, chlorine, bromine, C 1-5 alkyl, C 1-5 alkoxy or nitro, R" is C 1-5 alkyl, C 1-5 haloalkyl, C 2-5 alkenyl, C 2-5 haloalkenyl, or C 2-5 alkynyl, each of R"' and R"" is hydrogen, C 1-5 alkyl or phenyl or in combination they form a pentamethylene or tetramethylene chain, Y is hydrogen or fluorine, Z is hydrogen, fluorine, chlorine, trifluoromethyl or pentafluoroethyl and "halo" is fluorine, chlorine or bromine. The compositions may contain other insecticides, for example rotenone, natural or synthetic esters of chrysanthemic acid and its derivatives, including pyrethrin and allethrin, chlorinated hydrocarbons, including BHC, lindane, chlordane, heptachlor, toxaphene, aldrin, dieldrin, endrin, DDT (Trade Mark), TDE and methoxychlor, organic phosphates, including TEPP, phosphamiden, demeton, Malathion (Trade Mark), ethion, dimethoate, mecarban, methyl parathion, parathion, 0-2, 4-dichlorophenyl - O - methyl - phosphoramidothioate, Ronnel (Trade Mark), 0 - 4 - t - butyl - 2 - chlorophenyl - O - methyl - methyl phosphoramidate, tepa, metapa, diazinon and Metasystox (Trade Mark), sulphites, including 2 - p - t - butyl - phenoxy - 1 - methyl - ethyl - 2 - chlorethyl - sulphite, and carbamates, including 4- dimethylamino - 3,5 - xylylmethyl - carbamate and carbaryl. Reference has been directed by the Comptroller to Specifications 1,170,737, 1,151,424, 1,104,936, and 1,087,561.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US72654068A | 1968-05-03 | 1968-05-03 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1267998A true GB1267998A (en) | 1972-03-22 |
Family
ID=24919017
Family Applications (3)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB22589/69A Expired GB1267998A (en) | 1968-05-03 | 1969-05-02 | Insecticidal and acaricidal benzimidazole compositions |
| GB57611/70A Expired GB1267999A (en) | 1968-05-03 | 1969-05-02 | Benzimidazoles and a process for their preparation |
| GB57613/70A Expired GB1268000A (en) | 1968-05-03 | 1969-05-02 | Benzimidazoles and a process for their preparation |
Family Applications After (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB57611/70A Expired GB1267999A (en) | 1968-05-03 | 1969-05-02 | Benzimidazoles and a process for their preparation |
| GB57613/70A Expired GB1268000A (en) | 1968-05-03 | 1969-05-02 | Benzimidazoles and a process for their preparation |
Country Status (17)
| Country | Link |
|---|---|
| JP (1) | JPS5636165B1 (en) |
| BE (1) | BE732415A (en) |
| BG (3) | BG19163A3 (en) |
| CH (1) | CH509756A (en) |
| CS (1) | CS208686B2 (en) |
| DE (2) | DE1966823C3 (en) |
| EG (1) | EG9285A (en) |
| ES (2) | ES366718A1 (en) |
| FR (1) | FR2007808B1 (en) |
| GB (3) | GB1267998A (en) |
| HK (3) | HK17176A (en) |
| IL (1) | IL32074A (en) |
| MY (3) | MY7500102A (en) |
| NL (1) | NL158365B (en) |
| PH (1) | PH9655A (en) |
| RO (2) | RO62449A (en) |
| YU (2) | YU35357B (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3621301A1 (en) * | 1986-06-25 | 1988-01-07 | Bayer Ag | 2-TRIFLUORMETHYL-BENZIMIDAZOLE |
| EP2878198B1 (en) | 2013-11-29 | 2016-09-14 | Flügel GmbH | Method for attraction of cambiophagous, xylophagous and/or myzetophagous insects |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE659384A (en) * | 1965-02-05 | 1965-08-05 | Fisons Pest Control Ltd | Herbicidal and parasiticidal composition. |
| US3632397A (en) * | 1966-01-26 | 1972-01-04 | Lilly Co Eli | Method of controlling weeds pre-emergently |
-
1969
- 1969-04-23 EG EG221/69*A patent/EG9285A/en active
- 1969-04-25 IL IL32074A patent/IL32074A/en unknown
- 1969-04-30 BG BG016232A patent/BG19163A3/en unknown
- 1969-04-30 BG BG016231A patent/BG17584A3/en unknown
- 1969-04-30 YU YU1064/69A patent/YU35357B/en unknown
- 1969-04-30 BG BG12151A patent/BG17437A3/xx unknown
- 1969-05-02 FR FR6914147A patent/FR2007808B1/fr not_active Expired
- 1969-05-02 GB GB22589/69A patent/GB1267998A/en not_active Expired
- 1969-05-02 BE BE732415D patent/BE732415A/xx unknown
- 1969-05-02 DE DE1966823A patent/DE1966823C3/en not_active Expired
- 1969-05-02 JP JP3446769A patent/JPS5636165B1/ja active Pending
- 1969-05-02 DE DE19691922572 patent/DE1922572A1/en not_active Withdrawn
- 1969-05-02 PH PH10284*UA patent/PH9655A/en unknown
- 1969-05-02 ES ES366718A patent/ES366718A1/en not_active Expired
- 1969-05-02 GB GB57611/70A patent/GB1267999A/en not_active Expired
- 1969-05-02 GB GB57613/70A patent/GB1268000A/en not_active Expired
- 1969-05-04 CS CS693152A patent/CS208686B2/en unknown
- 1969-05-05 CH CH684869A patent/CH509756A/en not_active IP Right Cessation
- 1969-05-05 RO RO6900071823A patent/RO62449A/en unknown
- 1969-05-05 RO RO59885A patent/RO55895A/ro unknown
- 1969-05-05 NL NL6906852.A patent/NL158365B/en not_active IP Right Cessation
-
1971
- 1971-01-15 ES ES387295A patent/ES387295A1/en not_active Expired
-
1974
- 1974-08-16 YU YU2257/74A patent/YU35586B/en unknown
-
1975
- 1975-12-30 MY MY102/75A patent/MY7500102A/en unknown
- 1975-12-30 MY MY100/75A patent/MY7500100A/en unknown
- 1975-12-30 MY MY101/75A patent/MY7500101A/en unknown
-
1976
- 1976-03-25 HK HK171/76*UA patent/HK17176A/en unknown
- 1976-03-25 HK HK169/76*UA patent/HK16976A/en unknown
- 1976-03-25 HK HK170/76*UA patent/HK17076A/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| IL32074A (en) | 1975-10-15 |
| PH9655A (en) | 1976-01-27 |
| YU106469A (en) | 1980-06-30 |
| DE1966823C3 (en) | 1981-04-30 |
| NL6906852A (en) | 1969-11-05 |
| ES366718A1 (en) | 1971-07-16 |
| BG17584A3 (en) | 1973-11-10 |
| CH509756A (en) | 1971-07-15 |
| DE1966823A1 (en) | 1974-09-05 |
| MY7500100A (en) | 1975-12-31 |
| DE1966823B2 (en) | 1980-08-28 |
| GB1268000A (en) | 1972-03-22 |
| GB1267999A (en) | 1972-03-22 |
| YU35586B (en) | 1981-04-30 |
| BE732415A (en) | 1969-11-03 |
| CS208686B2 (en) | 1981-09-15 |
| NL158365B (en) | 1978-11-15 |
| DE1922572A1 (en) | 1969-11-13 |
| MY7500101A (en) | 1975-12-31 |
| EG9285A (en) | 1976-11-30 |
| MY7500102A (en) | 1975-12-31 |
| RO55895A (en) | 1974-02-01 |
| HK17076A (en) | 1976-04-02 |
| YU35357B (en) | 1980-12-31 |
| HK16976A (en) | 1976-04-02 |
| FR2007808A1 (en) | 1970-01-09 |
| HK17176A (en) | 1976-04-02 |
| JPS5636165B1 (en) | 1981-08-22 |
| YU225774A (en) | 1980-10-31 |
| ES387295A1 (en) | 1974-01-01 |
| IL32074A0 (en) | 1969-06-25 |
| FR2007808B1 (en) | 1976-07-23 |
| BG17437A3 (en) | 1973-11-10 |
| RO62449A (en) | 1978-01-15 |
| BG19163A3 (en) | 1975-04-30 |
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