GB1104893A - Imino-dithiole derivatives and their use as pesticides - Google Patents
Imino-dithiole derivatives and their use as pesticidesInfo
- Publication number
- GB1104893A GB1104893A GB51574/65A GB5157465A GB1104893A GB 1104893 A GB1104893 A GB 1104893A GB 51574/65 A GB51574/65 A GB 51574/65A GB 5157465 A GB5157465 A GB 5157465A GB 1104893 A GB1104893 A GB 1104893A
- Authority
- GB
- United Kingdom
- Prior art keywords
- alkyl
- substituted
- group
- amido
- formula
- 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
- 239000000575 pesticide Substances 0.000 title abstract 2
- MZCLLPIAZHLJMB-UHFFFAOYSA-N 1-imino-3H-dithiole Chemical class N=S1SCC=C1 MZCLLPIAZHLJMB-UHFFFAOYSA-N 0.000 title 1
- 125000000217 alkyl group Chemical group 0.000 abstract 7
- 125000003368 amide group Chemical group 0.000 abstract 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 4
- 239000000203 mixture Substances 0.000 abstract 3
- 239000004215 Carbon black (E152) Chemical group 0.000 abstract 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 2
- 125000002252 acyl group Chemical group 0.000 abstract 2
- 125000004390 alkyl sulfonyl group Chemical group 0.000 abstract 2
- 125000003277 amino group Chemical group 0.000 abstract 2
- 125000003118 aryl group Chemical group 0.000 abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 239000000839 emulsion Substances 0.000 abstract 2
- 125000005843 halogen group Chemical group 0.000 abstract 2
- 125000000623 heterocyclic group Chemical group 0.000 abstract 2
- 229930195733 hydrocarbon Chemical group 0.000 abstract 2
- 125000001183 hydrocarbyl group Chemical group 0.000 abstract 2
- 229910052739 hydrogen Inorganic materials 0.000 abstract 2
- 239000001257 hydrogen Substances 0.000 abstract 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 2
- 229920006395 saturated elastomer Polymers 0.000 abstract 2
- 125000000547 substituted alkyl group Chemical group 0.000 abstract 2
- 125000003107 substituted aryl group Chemical group 0.000 abstract 2
- 239000004094 surface-active agent Substances 0.000 abstract 2
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 1
- 239000004372 Polyvinyl alcohol Substances 0.000 abstract 1
- 239000004480 active ingredient Substances 0.000 abstract 1
- 239000000443 aerosol Substances 0.000 abstract 1
- 230000003115 biocidal effect Effects 0.000 abstract 1
- 239000005018 casein Substances 0.000 abstract 1
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 abstract 1
- 235000021240 caseins Nutrition 0.000 abstract 1
- 229920003086 cellulose ether Polymers 0.000 abstract 1
- 239000000084 colloidal system Substances 0.000 abstract 1
- 239000012141 concentrate Substances 0.000 abstract 1
- 239000002270 dispersing agent Substances 0.000 abstract 1
- RWIUQKWSQMMBQD-UHFFFAOYSA-N dithiol-3-imine Chemical compound N=C1C=CSS1 RWIUQKWSQMMBQD-UHFFFAOYSA-N 0.000 abstract 1
- 239000000428 dust Substances 0.000 abstract 1
- 239000004495 emulsifiable concentrate Substances 0.000 abstract 1
- 239000003995 emulsifying agent Substances 0.000 abstract 1
- 239000012530 fluid Substances 0.000 abstract 1
- 239000003292 glue Substances 0.000 abstract 1
- 239000008187 granular material Substances 0.000 abstract 1
- 239000004009 herbicide Substances 0.000 abstract 1
- 239000004615 ingredient Substances 0.000 abstract 1
- 239000000463 material Substances 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 229920002451 polyvinyl alcohol Polymers 0.000 abstract 1
- 230000001681 protective effect Effects 0.000 abstract 1
- 235000019830 sodium polyphosphate Nutrition 0.000 abstract 1
- 239000007787 solid Substances 0.000 abstract 1
- 239000003381 stabilizer Substances 0.000 abstract 1
- 239000004563 wettable powder Substances 0.000 abstract 1
- 239000000080 wetting agent Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
-
- G—PHYSICS
- G05—CONTROLLING; REGULATING
- G05D—SYSTEMS FOR CONTROLLING OR REGULATING NON-ELECTRIC VARIABLES
- G05D1/00—Control of position, course, altitude or attitude of land, water, air or space vehicles, e.g. using automatic pilots
- G05D1/0055—Control of position, course, altitude or attitude of land, water, air or space vehicles, e.g. using automatic pilots with safety arrangements
- G05D1/0077—Control of position, course, altitude or attitude of land, water, air or space vehicles, e.g. using automatic pilots with safety arrangements using redundant signals or controls
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Aviation & Aerospace Engineering (AREA)
- Radar, Positioning & Navigation (AREA)
- Remote Sensing (AREA)
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Automation & Control Theory (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
Compounds of the formula <FORM:1104893/C2/1> wherein R1 represents an alkyl, substituted alkyl, aryl, substituted aryl, amino or hydrocarbon substituted amino group, or a heterocyclic ring system or a group of formula -OX, where X represents a hydrogen atom or an alkyl, acyl, amido, alkyl substituted amido or alkyl sulphonyl group; R2 and R3, which may be the same or different, each represent a hydrogen or halogen atom or a C1- 6 alkyl, phenyl or substituted phenyl group or R2 and R3 may, together with the carbon atoms of the dithiole ring to which they are attached, form a carbocyclic ring system which may be saturated or unsaturated, substituted or unsubstituted; or 1,1- or 2,2-dioxides thereof, may be prepared by conventional procedures. Many examples of the above compounds are given and some are claimed to be novel.ALSO:A biocidal composition comprises a carrier or surface active agent or both together with, as active ingredient, at least one 3-imino-1,2-dithiole of the formula: <FORM:1104893/A5-A6/1> wherein R1 represents an alkyl, substituted alkyl, aryl, substituted aryl, amino or hydrocarbon substituted amino group, or a heterocyclic ring system or a group of formula -OX where X represents a hydrogen atom or an alkyl, acyl, amido, alkyl substituted amido or alkyl sulphonyl group; R2 and R3, which may be the same or different, each represent a hydrogen or halogen atom or a C1-6 alkyl, phenyl or substituted phenyl group or R2 and R3 may, together with the carbon atoms of the dithiole ring to which they are attached, form a carbocyclic ring system which may be saturated or unsaturated, substituted or unsubstituted; or 1,1- or 2,2- dioxides thereof. The carrier, which may be a solid or a fluid, may be organic or inorganic and of synthetic or natural origin, the surface active agent, which may be ionic or nonionic, may be a wetting agent, an emulsifying agent or a dispersing agent and the composition may be formulated as a wettable powder, a dust, a concentrate, a solution, a conventional emulsion, an emulsifiable concentrate, an invert emulsion, an aerosol, granules or an encapsulated material. The composition may contain other ingredients such as protective colloids, glue, casein, gums and polyvinyl alcohol, sodium polyphosphates, cellulose ethers, stabilisers, other unspecified herbicides or pesticides, and stickers.
Priority Applications (7)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US598222A US3414653A (en) | 1965-12-06 | 1966-12-01 | Compositions and methods for controlling fungi using 3-imino-1,2-dithiole compounds |
| DE19661567143 DE1567143A1 (en) | 1965-12-06 | 1966-12-05 | Pest control agent with 3-imino-1,2-dithiol derivatives as active ingredient |
| FR86116A FR1504150A (en) | 1965-12-06 | 1966-12-05 | Pesticide compositions containing 3-imino-1, 2-dithiol derivatives, new 3-imino-1, 2-dithiols, and their use |
| CH243067A CH483193A (en) | 1965-12-06 | 1967-02-20 | Pesticide with 3-imino-1,2-dithiol derivatives as the active component |
| FR1548718D FR1548718A (en) | 1965-12-06 | 1967-11-16 | |
| US683496A US3509435A (en) | 1965-12-06 | 1967-11-16 | Mechanically cross-coupled dual channel actuator system |
| DE19671531456 DE1531456A1 (en) | 1965-12-06 | 1967-11-17 | Transmission system |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB5157466 | 1966-11-17 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1104893A true GB1104893A (en) | 1968-03-06 |
Family
ID=10460544
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB51574/65A Expired GB1104893A (en) | 1965-12-06 | 1965-12-06 | Imino-dithiole derivatives and their use as pesticides |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB1104893A (en) |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4163059A (en) * | 1976-08-21 | 1979-07-31 | Bayer Aktiengesellschaft | Pesticidally active 4,5-dichloro-3-substituted-phenylimino-1,2-dithiolenes |
| EP0249328A2 (en) * | 1986-05-23 | 1987-12-16 | Imperial Chemical Industries Plc | Heterocyclic thione compounds and their use as biocides |
| US5187172A (en) * | 1986-05-23 | 1993-02-16 | Imperial Chemical Industries Plc | Biocides |
| US5596102A (en) * | 1986-05-23 | 1997-01-21 | Zeneca Limited | Biocides |
| JP2019116479A (en) * | 2019-02-13 | 2019-07-18 | 株式会社Adeka | Novel compound |
| CN114524798A (en) * | 2022-01-14 | 2022-05-24 | 华南师范大学 | Benzodithiocarbazaheterocycle derivative and preparation method and application thereof |
-
1965
- 1965-12-06 GB GB51574/65A patent/GB1104893A/en not_active Expired
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4163059A (en) * | 1976-08-21 | 1979-07-31 | Bayer Aktiengesellschaft | Pesticidally active 4,5-dichloro-3-substituted-phenylimino-1,2-dithiolenes |
| EP0249328A2 (en) * | 1986-05-23 | 1987-12-16 | Imperial Chemical Industries Plc | Heterocyclic thione compounds and their use as biocides |
| EP0249328A3 (en) * | 1986-05-23 | 1990-05-23 | Imperial Chemical Industries Plc | Heterocyclic thione compounds and their use as biocides |
| US5187172A (en) * | 1986-05-23 | 1993-02-16 | Imperial Chemical Industries Plc | Biocides |
| US5596102A (en) * | 1986-05-23 | 1997-01-21 | Zeneca Limited | Biocides |
| JP2019116479A (en) * | 2019-02-13 | 2019-07-18 | 株式会社Adeka | Novel compound |
| CN114524798A (en) * | 2022-01-14 | 2022-05-24 | 华南师范大学 | Benzodithiocarbazaheterocycle derivative and preparation method and application thereof |
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