GB1567482A - Pesticidal use of benzodithioles - Google Patents
Pesticidal use of benzodithioles Download PDFInfo
- Publication number
- GB1567482A GB1567482A GB6507/79A GB650779A GB1567482A GB 1567482 A GB1567482 A GB 1567482A GB 6507/79 A GB6507/79 A GB 6507/79A GB 650779 A GB650779 A GB 650779A GB 1567482 A GB1567482 A GB 1567482A
- Authority
- GB
- United Kingdom
- Prior art keywords
- compound
- formula
- plants
- soil
- benzodithiole
- 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
- 230000000361 pesticidal effect Effects 0.000 title claims description 4
- WHGMHGPIJZTKTI-UHFFFAOYSA-N 3h-1,2-benzodithiole Chemical class C1=CC=C2CSSC2=C1 WHGMHGPIJZTKTI-UHFFFAOYSA-N 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims description 37
- 239000002689 soil Substances 0.000 claims description 24
- 239000000203 mixture Substances 0.000 claims description 10
- 238000000034 method Methods 0.000 claims description 9
- 241000607479 Yersinia pestis Species 0.000 claims description 8
- IZTJMBFHQMPFKL-UHFFFAOYSA-N 1,3-benzodithiol-2-one Chemical compound C1=CC=C2SC(=O)SC2=C1 IZTJMBFHQMPFKL-UHFFFAOYSA-N 0.000 claims description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 3
- 239000008187 granular material Substances 0.000 claims description 3
- 229910052739 hydrogen Inorganic materials 0.000 claims description 3
- 239000001257 hydrogen Substances 0.000 claims description 3
- 239000003701 inert diluent Substances 0.000 claims description 3
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 3
- 229960000892 attapulgite Drugs 0.000 claims description 2
- 239000004927 clay Substances 0.000 claims description 2
- 239000003337 fertilizer Substances 0.000 claims description 2
- 229910052625 palygorskite Inorganic materials 0.000 claims description 2
- 239000003415 peat Substances 0.000 claims description 2
- 229910052902 vermiculite Inorganic materials 0.000 claims description 2
- 235000019354 vermiculite Nutrition 0.000 claims description 2
- 239000010455 vermiculite Substances 0.000 claims description 2
- 239000000080 wetting agent Substances 0.000 claims description 2
- ZJGPITKKLNFPGK-UHFFFAOYSA-N 5-nitro-1,3-benzodithiol-2-one Chemical compound [O-][N+](=O)C1=CC=C2SC(=O)SC2=C1 ZJGPITKKLNFPGK-UHFFFAOYSA-N 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 claims 1
- 239000003085 diluting agent Substances 0.000 claims 1
- 241000196324 Embryophyta Species 0.000 description 29
- 230000000855 fungicidal effect Effects 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 239000002904 solvent Substances 0.000 description 7
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 6
- 238000011282 treatment Methods 0.000 description 6
- 230000000895 acaricidal effect Effects 0.000 description 5
- 230000001069 nematicidal effect Effects 0.000 description 5
- 238000012360 testing method Methods 0.000 description 5
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- 244000046052 Phaseolus vulgaris Species 0.000 description 4
- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 4
- 230000002363 herbicidal effect Effects 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 240000008067 Cucumis sativus Species 0.000 description 3
- 235000010799 Cucumis sativus var sativus Nutrition 0.000 description 3
- 238000010348 incorporation Methods 0.000 description 3
- 208000015181 infectious disease Diseases 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 241000238876 Acari Species 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 241000233866 Fungi Species 0.000 description 2
- 241000244206 Nematoda Species 0.000 description 2
- 240000003768 Solanum lycopersicum Species 0.000 description 2
- 241001454293 Tetranychus urticae Species 0.000 description 2
- 239000000642 acaricide Substances 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 230000002538 fungal effect Effects 0.000 description 2
- 239000000417 fungicide Substances 0.000 description 2
- 239000002035 hexane extract Substances 0.000 description 2
- 230000000749 insecticidal effect Effects 0.000 description 2
- 239000005645 nematicide Substances 0.000 description 2
- LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- HCMLNPZTRYNCMA-UHFFFAOYSA-N 1,3-benzodithiole Chemical compound C1=CC=C2SCSC2=C1 HCMLNPZTRYNCMA-UHFFFAOYSA-N 0.000 description 1
- 241000213004 Alternaria solani Species 0.000 description 1
- 241000239223 Arachnida Species 0.000 description 1
- VYZAHLCBVHPDDF-UHFFFAOYSA-N Dinitrochlorobenzene Chemical compound [O-][N+](=O)C1=CC=C(Cl)C([N+]([O-])=O)=C1 VYZAHLCBVHPDDF-UHFFFAOYSA-N 0.000 description 1
- 239000004398 Ethyl lauroyl arginate Substances 0.000 description 1
- 241000238631 Hexapoda Species 0.000 description 1
- 241000243786 Meloidogyne incognita Species 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- -1 Nitro 1,3 benzodithiole Chemical compound 0.000 description 1
- 241000918584 Pythium ultimum Species 0.000 description 1
- 241000813090 Rhizoctonia solani Species 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 230000003115 biocidal effect Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000004495 emulsifiable concentrate Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 239000004009 herbicide Substances 0.000 description 1
- 239000002054 inoculum Substances 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- 230000009545 invasion Effects 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 235000015097 nutrients Nutrition 0.000 description 1
- 238000003359 percent control normalization Methods 0.000 description 1
- 239000000575 pesticide Substances 0.000 description 1
- 239000001965 potato dextrose agar Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000007363 ring formation reaction Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- WZWGGYFEOBVNLA-UHFFFAOYSA-N sodium;dihydrate Chemical compound O.O.[Na] WZWGGYFEOBVNLA-UHFFFAOYSA-N 0.000 description 1
- 239000008223 sterile water Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 230000009885 systemic effect Effects 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D339/00—Heterocyclic compounds containing rings having two sulfur atoms as the only ring hetero atoms
- C07D339/02—Five-membered rings
- C07D339/06—Five-membered rings having the hetero atoms in positions 1 and 3, e.g. cyclic dithiocarbonates
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Heterocyclic Compounds Containing Sulfur Atoms (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US05/618,255 US4084954A (en) | 1975-09-30 | 1975-09-30 | Biocidally-active 1,3-benzodithiole-2-one compounds |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1567482A true GB1567482A (en) | 1980-05-14 |
Family
ID=24476962
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB6507/79A Expired GB1567482A (en) | 1975-09-30 | 1976-09-30 | Pesticidal use of benzodithioles |
| GB40675/76A Expired GB1567481A (en) | 1975-09-30 | 1976-09-30 | Benzodithiole derivatives |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB40675/76A Expired GB1567481A (en) | 1975-09-30 | 1976-09-30 | Benzodithiole derivatives |
Country Status (14)
| Country | Link |
|---|---|
| US (2) | US4084954A (en, 2012) |
| JP (1) | JPS5265270A (en, 2012) |
| AR (1) | AR221323A1 (en, 2012) |
| AU (1) | AU503926B2 (en, 2012) |
| BE (1) | BE846802A (en, 2012) |
| BR (1) | BR7606511A (en, 2012) |
| CA (1) | CA1071200A (en, 2012) |
| CH (1) | CH620338A5 (en, 2012) |
| DE (1) | DE2644036A1 (en, 2012) |
| FR (1) | FR2326424A1 (en, 2012) |
| GB (2) | GB1567482A (en, 2012) |
| MX (1) | MX4134E (en, 2012) |
| NL (1) | NL7610834A (en, 2012) |
| SE (1) | SE7610167L (en, 2012) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4084954A (en) * | 1975-09-30 | 1978-04-18 | The Ansul Company | Biocidally-active 1,3-benzodithiole-2-one compounds |
| FR2399210A1 (fr) * | 1977-08-04 | 1979-03-02 | Ansul Co | Produit antiparasitaire a base de 1,3-benzodithiole-2-thione |
| US4287204A (en) * | 1979-04-25 | 1981-09-01 | Ciba-Geigy Corporation | 1,3-Benzodithiol-2-ones |
| US4240821A (en) * | 1979-11-08 | 1980-12-23 | Ciba-Geigy Corporation | Biocidally-active 1,3-benzodithiole-2-thione compounds |
| US5833944A (en) * | 1994-11-07 | 1998-11-10 | Hybridon, Inc. | Procedure for the solid phase synthesis of 35 S-labeled oligonucleotides with 3H-1,2-benzodithiol-3-one-1,1-dioxide |
| US8470741B2 (en) * | 2003-05-07 | 2013-06-25 | Croda Americas Llc | Homogeneous liquid saccharide and oil systems |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB823251A (en) * | 1955-07-02 | 1959-11-11 | Thomae Gmbh Dr K | Improvements in or relating to preparations containing benzoxathiol derivatives for the care of hair and skin |
| US3491119A (en) * | 1967-01-19 | 1970-01-20 | Standard Oil Co | Benzotrithiolanes and their preparation |
| US3818041A (en) * | 1969-09-10 | 1974-06-18 | Standard Oil Co | Process for preparing aromatic cyclic thiones |
| US4084954A (en) * | 1975-09-30 | 1978-04-18 | The Ansul Company | Biocidally-active 1,3-benzodithiole-2-one compounds |
-
1975
- 1975-09-30 US US05/618,255 patent/US4084954A/en not_active Expired - Lifetime
-
1976
- 1976-09-14 SE SE7610167A patent/SE7610167L/xx not_active Application Discontinuation
- 1976-09-28 CA CA262,195A patent/CA1071200A/en not_active Expired
- 1976-09-29 BR BR7606511A patent/BR7606511A/pt unknown
- 1976-09-29 CH CH1230576A patent/CH620338A5/fr not_active IP Right Cessation
- 1976-09-29 FR FR7629310A patent/FR2326424A1/fr active Granted
- 1976-09-29 JP JP51118400A patent/JPS5265270A/ja active Pending
- 1976-09-30 NL NL7610834A patent/NL7610834A/xx not_active Application Discontinuation
- 1976-09-30 GB GB6507/79A patent/GB1567482A/en not_active Expired
- 1976-09-30 DE DE19762644036 patent/DE2644036A1/de not_active Withdrawn
- 1976-09-30 GB GB40675/76A patent/GB1567481A/en not_active Expired
- 1976-09-30 AR AR264928A patent/AR221323A1/es active
- 1976-09-30 BE BE171123A patent/BE846802A/xx unknown
- 1976-09-30 AU AU18287/76A patent/AU503926B2/en not_active Expired
- 1976-10-01 MX MX764947U patent/MX4134E/es unknown
-
1977
- 1977-08-04 US US05/821,978 patent/US4139362A/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| CH620338A5 (en, 2012) | 1980-11-28 |
| FR2326424A1 (fr) | 1977-04-29 |
| US4139362A (en) | 1979-02-13 |
| AR221323A1 (es) | 1981-01-30 |
| GB1567481A (en) | 1980-05-14 |
| NL7610834A (nl) | 1977-04-01 |
| FR2326424B1 (en, 2012) | 1981-10-09 |
| CA1071200A (en) | 1980-02-05 |
| SE7610167L (sv) | 1977-03-31 |
| AU503926B2 (en) | 1979-09-27 |
| BR7606511A (pt) | 1977-07-05 |
| AU1828776A (en) | 1978-04-06 |
| MX4134E (es) | 1982-01-06 |
| JPS5265270A (en) | 1977-05-30 |
| DE2644036A1 (de) | 1977-04-14 |
| BE846802A (fr) | 1977-01-17 |
| US4084954A (en) | 1978-04-18 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed [section 19, patents act 1949] | ||
| PCNP | Patent ceased through non-payment of renewal fee |