DE1024745B - Gastropoden-Bekaempfungsmittel - Google Patents
Gastropoden-BekaempfungsmittelInfo
- Publication number
- DE1024745B DE1024745B DEF18509A DEF0018509A DE1024745B DE 1024745 B DE1024745 B DE 1024745B DE F18509 A DEF18509 A DE F18509A DE F0018509 A DEF0018509 A DE F0018509A DE 1024745 B DE1024745 B DE 1024745B
- Authority
- DE
- Germany
- Prior art keywords
- trichloro
- nitrosalicylanilide
- gastropod
- nitro
- acetoxybenzanilide
- 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.)
- Pending
Links
- 241000237858 Gastropoda Species 0.000 title claims description 18
- 239000003795 chemical substances by application Substances 0.000 claims description 6
- 125000005843 halogen group Chemical group 0.000 claims description 5
- 239000004480 active ingredient Substances 0.000 claims description 3
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 3
- 125000001424 substituent group Chemical group 0.000 claims description 2
- 239000000843 powder Substances 0.000 claims 2
- 125000002252 acyl group Chemical group 0.000 claims 1
- -1 5,5'-dichloro-2'-methyl-4'-nitrosalicylanilide Chemical compound 0.000 description 12
- 150000001875 compounds Chemical class 0.000 description 5
- IZUPBVBPLAPZRR-UHFFFAOYSA-N pentachlorophenol Chemical compound OC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl IZUPBVBPLAPZRR-UHFFFAOYSA-N 0.000 description 4
- 241000282412 Homo Species 0.000 description 3
- 238000011161 development Methods 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- WKOAXDGOFPEFCC-UHFFFAOYSA-N 5-chloro-N-(2,5-dichloro-4-nitrophenyl)-2-hydroxybenzamide Chemical compound ClC1=CC=C(C(C(=O)NC2=C(C=C(C(=C2)Cl)[N+](=O)[O-])Cl)=C1)O WKOAXDGOFPEFCC-UHFFFAOYSA-N 0.000 description 2
- 241001465754 Metazoa Species 0.000 description 2
- 241000242678 Schistosoma Species 0.000 description 2
- 241000242541 Trematoda Species 0.000 description 2
- 241000869417 Trematodes Species 0.000 description 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 235000013601 eggs Nutrition 0.000 description 2
- 239000003995 emulsifying agent Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000003750 molluscacide Substances 0.000 description 2
- 230000002013 molluscicidal effect Effects 0.000 description 2
- 244000045947 parasite Species 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 201000004409 schistosomiasis Diseases 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- 239000000454 talc Substances 0.000 description 2
- 229910052623 talc Inorganic materials 0.000 description 2
- AAOYLOCWJSLLJU-UHFFFAOYSA-N 1,2-bis(5-bromo-2-hydroxyphenyl)ethane-1,2-dione Chemical compound OC1=CC=C(Br)C=C1C(=O)C(=O)C1=CC(Br)=CC=C1O AAOYLOCWJSLLJU-UHFFFAOYSA-N 0.000 description 1
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 1
- USFZGCVGLNMJPL-UHFFFAOYSA-N 3,5-dichloro-n-(4-chlorophenyl)-2-hydroxybenzamide Chemical compound OC1=C(Cl)C=C(Cl)C=C1C(=O)NC1=CC=C(Cl)C=C1 USFZGCVGLNMJPL-UHFFFAOYSA-N 0.000 description 1
- HTXGLMUZXAFRII-UHFFFAOYSA-N 5-chloro-2-hydroxy-n-(4-nitrophenyl)benzamide Chemical compound OC1=CC=C(Cl)C=C1C(=O)NC1=CC=C([N+]([O-])=O)C=C1 HTXGLMUZXAFRII-UHFFFAOYSA-N 0.000 description 1
- HLVNFLKZAAKIIS-UHFFFAOYSA-N 5-chloro-n-(2,4-dichloro-6-nitrophenyl)-2-hydroxybenzamide Chemical compound OC1=CC=C(Cl)C=C1C(=O)NC1=C(Cl)C=C(Cl)C=C1[N+]([O-])=O HLVNFLKZAAKIIS-UHFFFAOYSA-N 0.000 description 1
- PXRYFUAYXXGZHX-UHFFFAOYSA-N 5-chloro-n-(2,5-dichloro-4-nitrophenyl)-2-hydroxy-3-methylbenzamide Chemical compound CC1=CC(Cl)=CC(C(=O)NC=2C(=CC(=C(Cl)C=2)[N+]([O-])=O)Cl)=C1O PXRYFUAYXXGZHX-UHFFFAOYSA-N 0.000 description 1
- AVULBMQWQQWAKG-UHFFFAOYSA-N 5-chloro-n-(2,6-dichloro-4-nitrophenyl)-2-hydroxybenzamide Chemical compound OC1=CC=C(Cl)C=C1C(=O)NC1=C(Cl)C=C([N+]([O-])=O)C=C1Cl AVULBMQWQQWAKG-UHFFFAOYSA-N 0.000 description 1
- WWZFLKFNYIFDQD-UHFFFAOYSA-N 5-chloro-n-(3,5-dichloro-2-nitrophenyl)-2-hydroxybenzamide Chemical compound OC1=CC=C(Cl)C=C1C(=O)NC1=CC(Cl)=CC(Cl)=C1[N+]([O-])=O WWZFLKFNYIFDQD-UHFFFAOYSA-N 0.000 description 1
- FKLGWJUBUPDJJI-UHFFFAOYSA-N 5-chloro-n-(3-chloro-4-nitrophenyl)-2-hydroxybenzamide Chemical compound OC1=CC=C(Cl)C=C1C(=O)NC1=CC=C([N+]([O-])=O)C(Cl)=C1 FKLGWJUBUPDJJI-UHFFFAOYSA-N 0.000 description 1
- JRHPJUCMRNXATL-UHFFFAOYSA-N 5-chloro-n-[2-chloro-5-(trifluoromethyl)phenyl]-2-hydroxybenzamide Chemical compound OC1=CC=C(Cl)C=C1C(=O)NC1=CC(C(F)(F)F)=CC=C1Cl JRHPJUCMRNXATL-UHFFFAOYSA-N 0.000 description 1
- NPGJBNOLEOSPOA-UHFFFAOYSA-N BrC1=CC=C(C(C(=O)NC2=C(C=C(C(=C2)Cl)[N+](=O)[O-])Cl)=C1)O Chemical compound BrC1=CC=C(C(C(=O)NC2=C(C=C(C(=C2)Cl)[N+](=O)[O-])Cl)=C1)O NPGJBNOLEOSPOA-UHFFFAOYSA-N 0.000 description 1
- SSYVHRLUBLUTIT-UHFFFAOYSA-N ClC=1C=C(C(=C(C(=O)NC2=C(C=C(C(=C2)Cl)[N+](=O)[O-])Cl)C=1)OC(C)=O)C Chemical compound ClC=1C=C(C(=C(C(=O)NC2=C(C=C(C(=C2)Cl)[N+](=O)[O-])Cl)C=1)OC(C)=O)C SSYVHRLUBLUTIT-UHFFFAOYSA-N 0.000 description 1
- ZPMURVVSPFWRPT-UHFFFAOYSA-N ClC=1C=CC(=C(C(=O)NC2=C(C=C(C(=C2)Cl)[N+](=O)[O-])Cl)C=1)OC(C)=O Chemical compound ClC=1C=CC(=C(C(=O)NC2=C(C=C(C(=C2)Cl)[N+](=O)[O-])Cl)C=1)OC(C)=O ZPMURVVSPFWRPT-UHFFFAOYSA-N 0.000 description 1
- 241000607479 Yersinia pestis Species 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 150000001447 alkali salts Chemical class 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 125000002490 anilino group Chemical class [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 239000002246 antineoplastic agent Substances 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 230000011681 asexual reproduction Effects 0.000 description 1
- 238000013465 asexual reproduction Methods 0.000 description 1
- 239000000440 bentonite Substances 0.000 description 1
- 229910000278 bentonite Inorganic materials 0.000 description 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 229910000365 copper sulfate Inorganic materials 0.000 description 1
- ARUVKPQLZAKDPS-UHFFFAOYSA-L copper(II) sulfate Chemical compound [Cu+2].[O-][S+2]([O-])([O-])[O-] ARUVKPQLZAKDPS-UHFFFAOYSA-L 0.000 description 1
- 229940127089 cytotoxic agent Drugs 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical compound C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 210000003608 fece Anatomy 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 208000015181 infectious disease Diseases 0.000 description 1
- 230000001418 larval effect Effects 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- CDYKTFABNOULII-UHFFFAOYSA-N n-(4-chlorophenyl)-2-hydroxy-5-nitrobenzamide Chemical compound OC1=CC=C([N+]([O-])=O)C=C1C(=O)NC1=CC=C(Cl)C=C1 CDYKTFABNOULII-UHFFFAOYSA-N 0.000 description 1
- RJMUSRYZPJIFPJ-UHFFFAOYSA-N niclosamide Chemical compound OC1=CC=C(Cl)C=C1C(=O)NC1=CC=C([N+]([O-])=O)C=C1Cl RJMUSRYZPJIFPJ-UHFFFAOYSA-N 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 229920000151 polyglycol Polymers 0.000 description 1
- 239000010695 polyglycol Substances 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 230000001568 sexual effect Effects 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/36—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids
- A01N37/38—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids having at least one oxygen or sulfur atom attached to an aromatic ring system
- A01N37/40—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids having at least one oxygen or sulfur atom attached to an aromatic ring system having at least one carboxylic group or a thio analogue, or a derivative thereof, and one oxygen or sulfur atom attached to the same aromatic ring system
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/44—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a nitrogen atom attached to the same carbon skeleton by a single or double bond, this nitrogen atom not being a member of a derivative or of a thio analogue of a carboxylic group, e.g. amino-carboxylic acids
- A01N37/48—Nitro-carboxylic acids; Derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C233/00—Carboxylic acid amides
- C07C233/01—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C233/12—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by halogen atoms or by nitro or nitroso groups
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Agronomy & Crop Science (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Priority Applications (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| BE551294D BE551294A (enrdf_load_stackoverflow) | 1955-09-26 | ||
| DEF18509A DE1024745B (de) | 1955-09-26 | 1955-09-26 | Gastropoden-Bekaempfungsmittel |
| CH352868D CH352868A (de) | 1955-09-26 | 1956-08-25 | Verwendung von Oxybenzylaniliden oder deren O-Acylderivaten oder Salzen als Gastropoden-Bekämpfungsmittel |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DEF18509A DE1024745B (de) | 1955-09-26 | 1955-09-26 | Gastropoden-Bekaempfungsmittel |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE1024745B true DE1024745B (de) | 1958-02-20 |
Family
ID=7088978
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DEF18509A Pending DE1024745B (de) | 1955-09-26 | 1955-09-26 | Gastropoden-Bekaempfungsmittel |
Country Status (3)
| Country | Link |
|---|---|
| BE (1) | BE551294A (enrdf_load_stackoverflow) |
| CH (1) | CH352868A (enrdf_load_stackoverflow) |
| DE (1) | DE1024745B (enrdf_load_stackoverflow) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1126374B (de) * | 1959-08-27 | 1962-03-29 | Bayer Ag | Verfahren zur Herstellung von Alkanolaminsalzen von Salicylaniliden |
| US3074848A (en) * | 1960-02-02 | 1963-01-22 | Bayer Ag | 2-hydroxy-5,2'-dichloro-4'-nitrobenzanilide for combating tapeworms |
| DE1148804B (de) * | 1961-03-14 | 1963-05-16 | Bayer Ag | Mittel zum Schutz gegen Termitenfrass |
-
0
- BE BE551294D patent/BE551294A/xx unknown
-
1955
- 1955-09-26 DE DEF18509A patent/DE1024745B/de active Pending
-
1956
- 1956-08-25 CH CH352868D patent/CH352868A/de unknown
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1126374B (de) * | 1959-08-27 | 1962-03-29 | Bayer Ag | Verfahren zur Herstellung von Alkanolaminsalzen von Salicylaniliden |
| US3074848A (en) * | 1960-02-02 | 1963-01-22 | Bayer Ag | 2-hydroxy-5,2'-dichloro-4'-nitrobenzanilide for combating tapeworms |
| DE1148804B (de) * | 1961-03-14 | 1963-05-16 | Bayer Ag | Mittel zum Schutz gegen Termitenfrass |
Also Published As
| Publication number | Publication date |
|---|---|
| BE551294A (enrdf_load_stackoverflow) | |
| CH352868A (de) | 1961-03-15 |
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