GB812512A - Compositions for combating nematodes - Google Patents
Compositions for combating nematodesInfo
- Publication number
- GB812512A GB812512A GB11785/57A GB1178557A GB812512A GB 812512 A GB812512 A GB 812512A GB 11785/57 A GB11785/57 A GB 11785/57A GB 1178557 A GB1178557 A GB 1178557A GB 812512 A GB812512 A GB 812512A
- Authority
- GB
- United Kingdom
- Prior art keywords
- benzothiazole
- nitro
- amino
- chloro
- atoms
- 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
- 241000244206 Nematoda Species 0.000 title 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 3
- KUCSJGBXJBQHNI-UHFFFAOYSA-N 2-chloro-6-nitro-1,3-benzothiazole Chemical compound [O-][N+](=O)C1=CC=C2N=C(Cl)SC2=C1 KUCSJGBXJBQHNI-UHFFFAOYSA-N 0.000 abstract 2
- DXYYSGDWQCSKKO-UHFFFAOYSA-N 2-methylbenzothiazole Chemical compound C1=CC=C2SC(C)=NC2=C1 DXYYSGDWQCSKKO-UHFFFAOYSA-N 0.000 abstract 2
- IOJUPLGTWVMSFF-UHFFFAOYSA-N benzothiazole Chemical compound C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 abstract 2
- 229910052736 halogen Inorganic materials 0.000 abstract 2
- 150000002367 halogens Chemical class 0.000 abstract 2
- 229910052739 hydrogen Inorganic materials 0.000 abstract 2
- 239000001257 hydrogen Substances 0.000 abstract 2
- 125000004435 hydrogen atom Chemical class [H]* 0.000 abstract 2
- BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical compound OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 abstract 2
- UHGULLIUJBCTEF-UHFFFAOYSA-N 2-aminobenzothiazole Chemical compound C1=CC=C2SC(N)=NC2=C1 UHGULLIUJBCTEF-UHFFFAOYSA-N 0.000 abstract 1
- ZCXGMSGCBDSEOY-UHFFFAOYSA-N 2-benzothiazolsulfonic acid Chemical compound C1=CC=C2SC(S(=O)(=O)O)=NC2=C1 ZCXGMSGCBDSEOY-UHFFFAOYSA-N 0.000 abstract 1
- DRLMMVPCYXFPEP-UHFFFAOYSA-N 2-bromo-1,3-benzothiazole Chemical compound C1=CC=C2SC(Br)=NC2=C1 DRLMMVPCYXFPEP-UHFFFAOYSA-N 0.000 abstract 1
- BSQLQMLFTHJVKS-UHFFFAOYSA-N 2-chloro-1,3-benzothiazole Chemical compound C1=CC=C2SC(Cl)=NC2=C1 BSQLQMLFTHJVKS-UHFFFAOYSA-N 0.000 abstract 1
- CVULGJIRGZVJHQ-UHFFFAOYSA-N 2-ethylbenzothiazole Chemical compound C1=CC=C2SC(CC)=NC2=C1 CVULGJIRGZVJHQ-UHFFFAOYSA-N 0.000 abstract 1
- VEWGTWPJKSPGCD-UHFFFAOYSA-N 2-methyl-5-nitro-1,3-benzothiazole Chemical compound [O-][N+](=O)C1=CC=C2SC(C)=NC2=C1 VEWGTWPJKSPGCD-UHFFFAOYSA-N 0.000 abstract 1
- NSYKYZBOQLCIHR-UHFFFAOYSA-N 2-nitro-1,3-benzothiazole Chemical compound C1=CC=C2SC([N+](=O)[O-])=NC2=C1 NSYKYZBOQLCIHR-UHFFFAOYSA-N 0.000 abstract 1
- AVVSRALHGMVQQW-UHFFFAOYSA-N 5-chloro-1,3-benzothiazol-2-amine Chemical compound ClC1=CC=C2SC(N)=NC2=C1 AVVSRALHGMVQQW-UHFFFAOYSA-N 0.000 abstract 1
- OMIHQJBWAPWLBO-UHFFFAOYSA-N 5-methoxy-1,3-benzothiazol-2-amine Chemical compound COC1=CC=C2SC(N)=NC2=C1 OMIHQJBWAPWLBO-UHFFFAOYSA-N 0.000 abstract 1
- AEUQLELVLDMMKB-UHFFFAOYSA-N 5-nitro-1,3-benzothiazole Chemical compound [O-][N+](=O)C1=CC=C2SC=NC2=C1 AEUQLELVLDMMKB-UHFFFAOYSA-N 0.000 abstract 1
- 239000004480 active ingredient Substances 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 125000005189 alkyl hydroxy group Chemical group 0.000 abstract 1
- 125000003277 amino group Chemical group 0.000 abstract 1
- 239000000440 bentonite Substances 0.000 abstract 1
- 229910000278 bentonite Inorganic materials 0.000 abstract 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 abstract 1
- 239000004927 clay Substances 0.000 abstract 1
- 229910052570 clay Inorganic materials 0.000 abstract 1
- 239000003995 emulsifying agent Substances 0.000 abstract 1
- 239000003337 fertilizer Substances 0.000 abstract 1
- 239000000417 fungicide Substances 0.000 abstract 1
- 230000001069 nematicidal effect Effects 0.000 abstract 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
- -1 nitro, amino Chemical group 0.000 abstract 1
- 239000000575 pesticide Substances 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 239000007787 solid Substances 0.000 abstract 1
- 239000000454 talc Substances 0.000 abstract 1
- 229910052623 talc Inorganic materials 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/60—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings condensed with carbocyclic rings or ring systems
- C07D277/62—Benzothiazoles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/60—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings condensed with carbocyclic rings or ring systems
- C07D277/62—Benzothiazoles
- C07D277/64—Benzothiazoles with only hydrocarbon or substituted hydrocarbon radicals attached in position 2
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/60—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings condensed with carbocyclic rings or ring systems
- C07D277/62—Benzothiazoles
- C07D277/68—Benzothiazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached in position 2
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/60—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings condensed with carbocyclic rings or ring systems
- C07D277/62—Benzothiazoles
- C07D277/68—Benzothiazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached in position 2
- C07D277/70—Sulfur atoms
- C07D277/76—Sulfur atoms attached to a second hetero atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/60—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings condensed with carbocyclic rings or ring systems
- C07D277/62—Benzothiazoles
- C07D277/68—Benzothiazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached in position 2
- C07D277/82—Nitrogen atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
A nematicidal composition consists essentially of a benzothiazole of the formula <FORM:0812512/VI/1> in which R stands for hydrogen, an alkyl radical containing 1-5 C atoms, nitro, halogen, sulphonic acid, a salt of sulphonic acid, or an amino group, and R1 stands for hydrogen, an alkyl group containing 1-5 C atoms, halogen, nitro, amino or an alkyl-hydroxy group containing 1-5 C atoms preferably in an amount up to 10 per cent by weight together with an inert solid carrier, e.g. chalk, talc, bentonite or clay, or with water containing an emulsifier. The compositions may include fertilizers, other pesticides, fungicides and the like. Specified active ingredients are 2-methyl-benzothiazole, 2-ethyl - benzothiazole, 2 - chloro - benzothiazole, 2 - bromo - benzothiazole, 2 - nitro - benzothiazole, 5 - nitro - benzothiazole, 2 - ahloro - 5-nitro - benzothiazole, 2 - chloro - 6 - nitrobenzothiazole, 2 - amino - benzothiazole, 2 - amino-5 - chloro - benzothiazole, 2 - amino - 5 - methoxy - benzothiazole, benzothiazole - 2 - sulphonic - acid, 2 - methyl - 5 - nitro - benzothiazole, 2-chloro-6-nitro-benzothiazole.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE812512X | 1956-04-12 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB812512A true GB812512A (en) | 1959-04-29 |
Family
ID=6730723
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB11785/57A Expired GB812512A (en) | 1956-04-12 | 1957-04-10 | Compositions for combating nematodes |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB812512A (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3382146A (en) * | 1962-09-13 | 1968-05-07 | Philips Corp | Method of protecting plants with 2, 1, 3-benzodithiadiazole compounds |
| US3513237A (en) * | 1967-03-28 | 1970-05-19 | Union Carbide Corp | Pesticidal 2-trihalomethylbenzothiazoles |
| US4731374A (en) * | 1984-12-22 | 1988-03-15 | Dr. Karl Thomae Gmbh | Tetrahydro-benzthiazoles, the preparation thereof and their use as intermediate products or as pharmaceuticals |
-
1957
- 1957-04-10 GB GB11785/57A patent/GB812512A/en not_active Expired
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3382146A (en) * | 1962-09-13 | 1968-05-07 | Philips Corp | Method of protecting plants with 2, 1, 3-benzodithiadiazole compounds |
| US3513237A (en) * | 1967-03-28 | 1970-05-19 | Union Carbide Corp | Pesticidal 2-trihalomethylbenzothiazoles |
| US4731374A (en) * | 1984-12-22 | 1988-03-15 | Dr. Karl Thomae Gmbh | Tetrahydro-benzthiazoles, the preparation thereof and their use as intermediate products or as pharmaceuticals |
| US4843086A (en) * | 1984-12-22 | 1989-06-27 | Boehringer Ingelheim Kg | Tetrahydro-benzthiazoles, the preparation thereof and their use as intermediate products or as pharmaceuticals |
| US4886812A (en) * | 1984-12-22 | 1989-12-12 | Dr. Karl Thomae Gmbh | Tetrahydro-benzthiazoles, the preparation thereof and their use as intermediate products or as pharmaceuticals |
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